Difference between revisions of "Timeline of leukemia"

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{{Attribute English Wikipedia|original-exists=yes}}
 
{{Attribute English Wikipedia|original-exists=yes}}
  
This is a '''timeline of [[leukemia]]''', describing especially major discoveries and advances in treatment against the disease.
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This is a '''timeline of [[wikipedia:leukemia|leukemia]]''', describing especially major discoveries and advances in treatment against the disease.
  
 
==Big picture==
 
==Big picture==
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! Year/period !! Key developments
 
! Year/period !! Key developments
 
|-
 
|-
|Prior to 1800||Various [[cancer]]s, including leukemia, are described in [[ancient Egypt]]ian texts dating back to 3000 BC. Translations inform "large, protruding mass" or "thick blood" and describe the disease as "there is no treatment." This basic understanding of leukemia and cancer lasts for millennia.<ref>{{cite web|title=History of Leukemia|url=http://leukemiainiraq.weebly.com/history-of-leukemia.html|accessdate=20 August 2016}}</ref>
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|Prior to 1800||Various [[wikipedia:cancer|cancer]]s, including leukemia, are described in [[wikipedia:ancient Egypt|ancient Egypt]]ian texts dating back to 3000 BC. Translations inform "large, protruding mass" or "thick blood" and describe the disease as "there is no treatment." This basic understanding of leukemia and cancer lasts for millennia.<ref>{{cite web|title=History of Leukemia|url=http://leukemiainiraq.weebly.com/history-of-leukemia.html|accessdate=20 August 2016}}</ref>
 
|-
 
|-
|19th Century||Discovery of leukemia. [[Alfred Velpeau|Velpeau]] (1825), [[Alfred Donné|Donné]] (1844), [[John Hughes Bennett|Bennett]] (1845), [[David Craigie|Craigie]] (1845), [[Rudolf Virchow|Virchow]] (1845), and [[Henry Fuller (physician)|Fuller]] (1846), establish the possibility that sustained [[leukocytosis]] could occur in the absence of infection. The term ''leukemia'' is adopted to describe such conditions.<ref name="the-leukemias"/><ref name="piller" /><ref name="Acute Myeloid Leukemia History" /> It is discovered that leukemia originates in the [[bone marrow]]. Histologic stains for microscopic study are introduced.<ref name="the-leukemias"/>
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|19th Century||Discovery of leukemia. [[wikipedia:Alfred Velpeau|Velpeau]] (1825), [[wikipedia:Alfred Donné|Donné]] (1844), [[wikipedia:John Hughes Bennett|Bennett]] (1845), [[wikipedia:David Craigie|Craigie]] (1845), [[wikipedia:Rudolf Virchow|Virchow]] (1845), and [[wikipedia:Henry Fuller (physician)|Fuller]] (1846), establish the possibility that sustained [[wikipedia:leukocytosis|leukocytosis]] could occur in the absence of infection. The term ''leukemia'' is adopted to describe such conditions.<ref name="the-leukemias"/><ref name="piller" /><ref name="Acute Myeloid Leukemia History" /> It is discovered that leukemia originates in the [[wikipedia:bone marrow|bone marrow]]. Histologic stains for microscopic study are introduced.<ref name="the-leukemias"/>
 
|-
 
|-
|1900s||Leukemia is subdivided in four primary types: [[acute myeloid leukemia]], [[chronic myeloid leukemia]], [[acute lymphocytic leukemia]] and [[chronic lymphocytic leukemia]].<ref>{{cite web|title=Leukemia types|url=http://www.cancercenter.com/leukemia/types/|accessdate=18 August 2016}}</ref><ref name="historia de la leucemia">{{cite web|title=La historia de la leucemia|url=http://lasaludi.info/historia-de-la-leucemia.html|accessdate=18 August 2016}}</ref>
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|1900s||Leukemia is subdivided in four primary types: [[wikipedia:acute myeloid leukemia|acute myeloid leukemia]], [[wikipedia:chronic myeloid leukemia|chronic myeloid leukemia]], [[wikipedia:acute lymphocytic leukemia|acute lymphocytic leukemia]] and [[wikipedia:chronic lymphocytic leukemia|chronic lymphocytic leukemia]].<ref>{{cite web|title=Leukemia types|url=http://www.cancercenter.com/leukemia/types/|accessdate=18 August 2016}}</ref><ref name="historia de la leucemia">{{cite web|title=La historia de la leucemia|url=http://lasaludi.info/historia-de-la-leucemia.html|accessdate=18 August 2016}}</ref>
 
|-
 
|-
|1940s–present||Era of [[chemotherapy]] development, also the first effective leukemia treatments with drugs introduced by [[Sidney Farber]].<ref name="piller" /><ref>{{cite web|title=Sidney Farber|url=http://www.dana-farber.org/About-Us/History-and-Milestones.aspx|accessdate=18 August 2016}}</ref><ref name=timeline/> Childhood leukemia is thought to be on a constant rise in the 20th and 21st century.<ref name="steadyhealth" /> In 2010, globally, approximately 281,500 people died of leukemia.<ref name=Loz2012>{{cite journal |vauthors= |title=Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010 |journal=Lancet |volume=380 |issue=9859 |pages=2095–128 |date=December 2012  |pmid=23245604 |doi=10.1016/S0140-6736(12)61728-0 |url=}}</ref> In 2000, approximately 256,000 children and adults around the world developed a form of leukemia, and 209,000 died from it.<ref name=Numbers>{{cite journal|title=Cancer incidence, mortality and survival by site for 14 regions of the world|author=Mathers, Colin D, Cynthia Boschi-Pinto, Alan D Lopez and Christopher JL Murray|work=Global Programme on Evidence for Health Policy Discussion Paper No. 13|publisher=World Health Organization|year=2001|url=http://www.who.int/entity/healthinfo/paper13.pdf}}</ref> DNA and genetic analysis have opened a new chapter in leukemia treatments.<ref name="steadyhealth">{{cite web|title=History of leukemia|url=http://ic.steadyhealth.com/history-of-leukemia|accessdate=19 August 2016}}</ref>
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|1940s–present||Era of [[wikipedia:chemotherapy|chemotherapy]] development, also the first effective leukemia treatments with drugs introduced by [[wikipedia:Sidney Farber|Sidney Farber]].<ref name="piller" /><ref>{{cite web|title=Sidney Farber|url=http://www.dana-farber.org/About-Us/History-and-Milestones.aspx|accessdate=18 August 2016}}</ref><ref name=timeline/> Childhood leukemia is thought to be on a constant rise in the 20th and 21st century.<ref name="steadyhealth" /> In 2010, globally, approximately 281,500 people died of leukemia.<ref name=Loz2012>{{cite journal |vauthors= |title=Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010 |journal=Lancet |volume=380 |issue=9859 |pages=2095–128 |date=December 2012  |pmid=23245604 |doi=10.1016/S0140-6736(12)61728-0 |url=}}</ref> In 2000, approximately 256,000 children and adults around the world developed a form of leukemia, and 209,000 died from it.<ref name=Numbers>{{cite journal|title=Cancer incidence, mortality and survival by site for 14 regions of the world|author=Mathers, Colin D, Cynthia Boschi-Pinto, Alan D Lopez and Christopher JL Murray|work=Global Programme on Evidence for Health Policy Discussion Paper No. 13|publisher=World Health Organization|year=2001|url=http://www.who.int/entity/healthinfo/paper13.pdf}}</ref> DNA and genetic analysis have opened a new chapter in leukemia treatments.<ref name="steadyhealth">{{cite web|title=History of leukemia|url=http://ic.steadyhealth.com/history-of-leukemia|accessdate=19 August 2016}}</ref>
 
|-
 
|-
 
|}
 
|}
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== Visual data ==
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[[File:Leukemia cases in the USA.png|400px|thumb|center|Evolution of new leukemia cases and deaths per 100,000 people in the United States for the period 1975-2013, according to the [[wikipedia:National Cancer Institute|National Cancer Institute]]. Age-adjusted.<ref>{{cite web|title=Leukemia cases USA|url=https://seer.cancer.gov/statfacts/html/ld/leuks.html|website=cancer.gov|accessdate=21 November 2016}}</ref>]]
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=== Google Trends ===
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The comparative chart below shows {{w|Google Trends}} data Leukemia (Syndrome) and Leukemia (Search Term), from January 2004 to March 2021, when the screenshot was taken. Interest is also ranked by country and displayed on world map.<ref>{{cite web |title=Leukemia |url=https://trends.google.com/trends/explore?date=all&q=%2Fm%2F04psf,Leukemia |website=Google Trends |access-date=8 March 2021}}</ref>
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[[File:Leukemia gt.png|thumb|center|600px]]
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=== Google Ngram Viewer ===
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The chart below shows {{w|Google Ngram Viewer}} data for Leukemia, from 1500 to 2019.<ref>{{cite web |title=Leukemia |url=https://books.google.com/ngrams/graph?content=Leukemia&year_start=1500&year_end=2019&corpus=26&smoothing=3&case_insensitive=true |website=books.google.com |access-date=8 March 2021 |language=en}}</ref>
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[[File:Leukemia ngram.png|thumb|center|700px]]
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=== Wikipedia Views ===
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The chart below shows pageviews of the English Wikipedia article {{w|Leukemia}}, on desktop from December 2007, and on mobile-web, desktop-spider, mobile-web-spider and mobile app, from July 2015; to February 2021.<ref>{{cite web |title=Leukemia |url=https://wikipediaviews.org/displayviewsformultiplemonths.php?page=Leukemia&allmonths=allmonths&language=en&drilldown=all |website=wikipediaviews.org |access-date=8 March 2021}}</ref>
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[[File:Leukemia wv.png|thumb|center|400px]]
 +
  
 
==Full timeline==
 
==Full timeline==
[[File:Leukemia cases in the USA.png|none|400px|thumb|Evolution of new leukemia cases and deaths per 100,000 people in the United States for the period 1975-2013, according to the [[National Cancer Institute]]. Age-adjusted.<ref>{{cite web|title=Leukemia cases USA|url=https://seer.cancer.gov/statfacts/html/ld/leuks.html|website=cancer.gov|accessdate=21 November 2016}}</ref>]]
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 +
 
 
{| class="sortable wikitable"
 
{| class="sortable wikitable"
 
! Year/period !! Type of event !! Event !!Location
 
! Year/period !! Type of event !! Event !!Location
 
|-
 
|-
|1749||Discovery||French physician [[Joseph Lieutaud]] first notes white cells, calling them ''globuli albicantes''.<ref name="from ancient times">{{cite web|title=Leukaemia – a brief historical review from ancient times to 1950|url=http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2141.2001.02411.x/full|accessdate=20 August 2016}}</ref>||  
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|1749||Discovery||French physician [[wikipedia:Joseph Lieutaud|Joseph Lieutaud]] first notes white cells, calling them ''globuli albicantes''.<ref name="from ancient times">{{cite web|title=Leukaemia – a brief historical review from ancient times to 1950|url=http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2141.2001.02411.x/full|accessdate=20 August 2016}}</ref>||
 +
|-
 +
|1774||Development||English surgeon [[wikipedia:William Hewson (surgeon)|William Hewson]] publishes work on the [[wikipedia:lymphatic system|lymphatic system]] and first describes the [[wikipedia:lymphocyte|lymphocyte]].<ref name="from ancient times" />||United Kingdom
 +
|-
 +
|1811||Development||Peter Cullen defines a case of ''splenitis acutus'' with unexplainable milky blood.<ref name="kampen">{{cite journal|last1=Kampen|first1=KR|title=The discovery and early understanding of leukemia.|doi=10.1016/j.leukres.2011.09.028|pmid=22033191|volume=36|date=Jan 2012|journal=Leuk Res|pages=6–13}}</ref>||[[wikipedia:Edinburgh|Edinburgh]], Scotland
 +
|-
 +
|1825||Development||French [[wikipedia:surgeon|surgeon]] [[wikipedia:Alfred-Armand-Louis-Marie Velpeau|Alfred Velpeau]] defines the leukemia associated symptoms, and observes [[wikipedia:pus|pus]] in the [[wikipedia:blood vessel|blood vessel]]s.<ref name="kampen" />||
 
|-
 
|-
|1774||Development||English surgeon [[William Hewson (surgeon)|William Hewson]] publishes work on the [[lymphatic system]] and first describes the [[lymphocyte]].<ref name="from ancient times" />||United Kingdom
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|1844||Discovery||French bacteriologist [[wikipedia:Alfred François Donné|Alfred Donné]] detects a maturation arrest of the [[wikipedia:white blood cell|white blood cell]]s.<ref name="kampen" />||
 
|-
 
|-
|1811||Development||Peter Cullen defines a case of ''splenitis acutus'' with unexplainable milky blood.<ref name="kampen">{{cite journal|last1=Kampen|first1=KR|title=The discovery and early understanding of leukemia.|doi=10.1016/j.leukres.2011.09.028|pmid=22033191|volume=36|date=Jan 2012|journal=Leuk Res|pages=6–13}}</ref>||[[Edinburgh]], Scotland
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|1845||Development|| English physician [[wikipedia:John Hughes Bennett|John Bennett]] renames ''splenitis acutus'' to ''leucocythemia'', based on the microscopic accumulation of purulent [[wikipedia:White blood cell|leukocytes]].<ref name="kampen" /><ref>{{cite web|title=splenitis acutus|url=http://leukemiaresearch12.wixsite.com/leukemiaresearch/about|accessdate=19 August 2016}}</ref>||  
 
|-
 
|-
|1825||Development||French [[surgeon]] [[Alfred-Armand-Louis-Marie Velpeau|Alfred Velpeau]] defines the leukemia associated symptoms, and observes [[pus]] in the [[blood vessel]]s.<ref name="kampen" />||
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|1845–1847||Development||German physician [[wikipedia:Rudolf Virchow|Rudolf Virchow]] defines a reversed [[wikipedia:White blood cell|white]] and [[wikipedia:red blood cell|red]] [[wikipedia:blood cell|blood cell]] balance. Virchow introduces the term ''leukemia'' for the disease (''leukämie'' in [[wikipedia:german language|German]]).<ref name="the-leukemias">{{cite web|title=The leukemias|url=http://jco.ascopubs.org/content/32/31/3463.extract#|accessdate=17 August 2016}}</ref><ref name="kampen" />||
 
|-
 
|-
|1844||Discovery||French bacteriologist [[Alfred François Donné|Alfred Donné]] detects a maturation arrest of the [[white blood cell]]s.<ref name="kampen" />||
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|1868||Discovery||German [[wikipedia:pathologist|pathologist]] [[wikipedia:Franz Ernst Christian Neumann|Ernst Neumann]] reports changes in the [[wikipedia:bone marrow|bone marrow]] in leukaemia and establishes the link between the source of blood and the bone marrow.<ref name="piller">{{cite web|title=Leukaemia – a brief historical review from ancient times to 1950|url=http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2141.2001.02411.x/full|accessdate=17 August 2016}}</ref>||[[wikipedia:Königsberg|Königsberg]], [[wikipedia:Prussia|Prussia]]
 
|-
 
|-
|1845||Development|| English physician [[John Hughes Bennett|John Bennett]] renames ''splenitis acutus'' to ''leucocythemia'', based on the microscopic accumulation of purulent [[White blood cell|leukocytes]].<ref name="kampen" /><ref>{{cite web|title=splenitis acutus|url=http://leukemiaresearch12.wixsite.com/leukemiaresearch/about|accessdate=19 August 2016}}</ref>||  
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| 1877 || Medical development || Swiss [[wikipedia:pathologist|pathologist]] [[wikipedia:Paul Ehrlich|Paul Ehrlich]] develops methods for staining tissue, making possible to distinguish between different types of blood cells, thus leading to the capability to diagnose numerous [[wikipedia:blood disease|blood disease]]s.<ref name="the-leukemias" /><ref name="piller" /><ref name="Acute Myeloid Leukemia History" />||Germany
 
|-
 
|-
|1845–1847||Development||German physician [[Rudolf Virchow]] defines a reversed [[White blood cell|white]] and [[red blood cell|red]] [[blood cell]] balance. Virchow introduces the term ''leukemia'' for the disease (''leukämie'' in [[german language|German]]).<ref name="the-leukemias">{{cite web|title=The leukemias|url=http://jco.ascopubs.org/content/32/31/3463.extract#|accessdate=17 August 2016}}</ref><ref name="kampen" />||
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| 1879 || Medical development || F. Mosler first describes the technique of bone marrow examination to diagnose leukemia.<ref name="Acute Myeloid Leukemia History" />||  
 
|-
 
|-
|1868||Discovery||German [[pathologist]] [[Franz Ernst Christian Neumann|Ernst Neumann]] reports changes in the [[bone marrow]] in leukaemia and establishes the link between the source of blood and the bone marrow.<ref name="piller">{{cite web|title=Leukaemia – a brief historical review from ancient times to 1950|url=http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2141.2001.02411.x/full|accessdate=17 August 2016}}</ref>||[[Königsberg]], [[Prussia]]
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| 1889 || Development || German physician [[wikipedia:Wilhelm Ebstein|Wilhelm Ebstein]] introduces the term ''acute leukemia'' to differentiate rapidly progressive and fatal leukemias from the more indolent chronic leukemias.<ref name="Acute Myeloid Leukemia History" />|| [[wikipedia:Prussia|Prussia]]
 
|-
 
|-
|1877||Development||Swiss [[pathologist]] [[Paul Ehrlich]] develops methods for staining tissue, making possible to distinguish between different types of blood cells, thus leading to the capability to diagnose numerous [[blood disease]]s.<ref name="the-leukemias" /><ref name="piller" /><ref name="Acute Myeloid Leukemia History" />||Germany
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| 1900 || Development || Swiss [[wikipedia:hematologist|hematologist]] [[wikipedia:Otto Naegeli|Otto Naegeli]] refines the classification of leukemia by dividing it into myelogenous and lymphocytic classes.<ref name="the-leukemias" /><ref name="piller" /><ref name="Acute Myeloid Leukemia History" />||
 
|-
 
|-
|1879||Development||F. Mosler first describes the technique of bone marrow examination to diagnose leukemia.<ref name="Acute Myeloid Leukemia History" />||  
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| 1936 || Medical development || American hematologist John H. Lawrence of the {{w|University of California, Berkeley}} introduces phosphorus-32 for the treatment of {{w|leukemia}}.<ref>{{cite book |last1=Marks |first1=Geoffrey |last2=Beatty |first2=William K. |title=The Precious Metals of Medicine |url=https://books.google.com.ar/books?id=QO5sAAAAMAAJ&q=%22in+1936%22+John+Lawrence+uses+phosphorus-32+to+treat+leukaemia&dq=%22in+1936%22+John+Lawrence+uses+phosphorus-32+to+treat+leukaemia&hl=en&sa=X&ved=0ahUKEwiP-JPz47jdAhWMHpAKHQNECI4Q6AEIMjAC}}</ref><ref>{{cite book |last1=Oreskes |first1=Naomi |last2=Krige |first2=John |title=Science and Technology in the Global Cold War |url=https://books.google.com.ar/books?id=FjMqBQAAQBAJ&pg=PA37&dq=%22in+1936%22+John+Lawrence+uses+phosphorus-32+to+treat+leukaemia&hl=en&sa=X&ved=0ahUKEwiP-JPz47jdAhWMHpAKHQNECI4Q6AEIKDAA#v=onepage&q=%22in%201936%22%20John%20Lawrence%20uses%20phosphorus-32%20to%20treat%20leukaemia&f=false}}</ref><ref>{{cite book |title=Positron Emission Tomography: Basic Sciences |edition=Dale L. Bailey, David W. Townsend, Peter E. Valk, Michael N. Maisey |url=https://books.google.com.ar/books?id=svliBnNd2LcC&pg=PR6&dq=%22in+1936%22+John+Lawrence+uses+phosphorus-32+to+treat+leukaemia&hl=en&sa=X&ved=0ahUKEwiP-JPz47jdAhWMHpAKHQNECI4Q6AEILTAB#v=onepage&q=%22in%201936%22%20John%20Lawrence%20uses%20phosphorus-32%20to%20treat%20leukaemia&f=false}}</ref> || {{w|United States}}
 
|-
 
|-
|1889||Development||German physician [[Wilhelm Ebstein]] introduces the term ''acute leukemia'' to differentiate rapidly progressive and fatal leukemias from the more indolent chronic leukemias.<ref name="Acute Myeloid Leukemia History" />||[[Prussia]]
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|1946||Organization||[[wikipedia:Leukemia Research Foundation|Leukemia Research Foundation]] is established. It is dedicated to combating all blood cancers by funding research.<ref>{{cite web|title=Leukemia Research Foundation|url=https://www.charitynavigator.org/index.cfm?bay=search.summary&orgid=8070|accessdate=17 August 2016}}</ref>||[[wikipedia:Northfield, Illinois|Northfield, Illinois]], [[wikipedia:United States|United States]]
 
|-
 
|-
|1900||Development||Swiss [[hematologist]] [[Otto Naegeli]] refines the classification of leukemia by dividing it into myelogenous and lymphocytic classes.<ref name="the-leukemias" /><ref name="piller" /><ref name="Acute Myeloid Leukemia History" />||
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|1947||Discovery||American [[wikipedia:pediatrics|pediatric]] [[wikipedia:pathologist|pathologist]] [[wikipedia:Sidney Farber|Sidney Farber]] discovers that [[wikipedia:aminopterin|aminopterin]] can induce remissions in acute [[wikipedia:lymphocytic leukemia|lymphocytic leukemia]] in children, leading to the development of a new category of chemotherapy drugs, called [[wikipedia:antimetabolites|antimetabolites]], that impair the ability of cancer cells to grow and replicate. It is considered the first effective leukemia treatment.<ref name=timeline>{{cite web|title=Leukemia Progress & Timeline|url=http://cancerprogress.net/timeline/leukemia|accessdate=16 August 2016}}</ref>||
 
|-
 
|-
|1946||Organization||[[Leukemia Research Foundation]] is established. It is dedicated to combating all blood cancers by funding research.<ref>{{cite web|title=Leukemia Research Foundation|url=https://www.charitynavigator.org/index.cfm?bay=search.summary&orgid=8070|accessdate=17 August 2016}}</ref>||[[Northfield, Illinois]], [[United States]]
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|1949||Organization||[[wikipedia:Leukemia & Lymphoma Society|Leukemia & Lymphoma Society]] is founded. It is the world's largest voluntary health organization dedicated to funding blood cancer research, education and patient services.<ref name="organizations">{{cite web|title=Leukemia Organizations|url=http://www.findingdulcinea.com/guides/Health/Cancer/Leukemia.pg_04.html|accessdate=17 August 2016}}</ref><ref name="Leukemia&Lymphoma">{{cite web|title=The Leukemia & Lymphoma Society|url=http://www.lls.org/who-we-are/history|accessdate=17 August 2016}}</ref>||[[wikipedia:Rye Brook|Rye Brook]], [[wikipedia:New York (state)|New York]] (serves the [[wikipedia:United States|United States]] and [[wikipedia:Canada|Canada]])
 
|-
 
|-
|1947||Discovery||American [[pediatrics|pediatric]] [[pathologist]] [[Sidney Farber]] discovers that [[aminopterin]] can induce remissions in acute [[lymphocytic leukemia]] in children, leading to the development of a new category of chemotherapy drugs, called [[antimetabolites]], that impair the ability of cancer cells to grow and replicate. It is considered the first effective leukemia treatment.<ref name=timeline>{{cite web|title=Leukemia Progress & Timeline|url=http://cancerprogress.net/timeline/leukemia|accessdate=16 August 2016}}</ref>||
+
|1949–1956||Discovery||Researchers discover ways to protect the body from [[wikipedia:radiation damage|radiation damage]] by shielding a mouse's [[wikipedia:spleen|spleen]] from radiation. Eventually, it is learned that the body recruits stem cells, which are found in the spleen and bone marrow, to protect and heal itself from radiation damage.<ref name="timeline" />||
 
|-
 
|-
|1949||Organization||[[Leukemia & Lymphoma Society]] is founded. It is the world's largest voluntary health organization dedicated to funding blood cancer research, education and patient services.<ref name="organizations">{{cite web|title=Leukemia Organizations|url=http://www.findingdulcinea.com/guides/Health/Cancer/Leukemia.pg_04.html|accessdate=17 August 2016}}</ref><ref name="Leukemia&Lymphoma">{{cite web|title=The Leukemia & Lymphoma Society|url=http://www.lls.org/who-we-are/history|accessdate=17 August 2016}}</ref>||[[Rye Brook]], [[New York (state)|New York]] (serves the [[United States]] and [[Canada]])
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|1957||Development||Researchers report the first [[wikipedia:bone marrow|bone marrow]] transplantation for treating leukemia, although with poor results. It would not be until the late 1970s when marrow transplantation becomes successful due to tissue matching.<ref>{{cite journal|last1=Tetsuya|first1=Ishii|last2=Koji|first2=Eto|title=Fetal stem cell transplantation: Past, present, and future|doi=10.4252/wjsc.v6.i4.404|pmid=25258662|pmc=4172669|volume=6|year=2014|journal=World J Stem Cells|pages=404–20}}</ref>||[[wikipedia:United States|United States]]
 
|-
 
|-
|1949–1956||Discovery||Researchers discover ways to protect the body from [[radiation damage]] by shielding a mouse's [[spleen]] from radiation. Eventually, it is learned that the body recruits stem cells, which are found in the spleen and bone marrow, to protect and heal itself from radiation damage.<ref name="timeline" />||
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|1958||Discovery||Scientists find that a combination of the drugs [[wikipedia:Mercaptopurine|6-mercaptopurine]] and [[wikipedia:methotrexate|methotrexate]] can reduce or eliminate cancer growth and extend survival in patients with leukemia. It is discovered that carefully honed drug combinations can attack cancer cells from different angles.<ref name="timeline" />||[[wikipedia:United States|United States]]
 
|-
 
|-
|1957||Development||Researchers report the first [[bone marrow]] transplantation for treating leukemia, although with poor results. It would not be until the late 1970s when marrow transplantation becomes successful due to tissue matching.<ref>{{cite journal|last1=Tetsuya|first1=Ishii|last2=Koji|first2=Eto|title=Fetal stem cell transplantation: Past, present, and future|doi=10.4252/wjsc.v6.i4.404|pmid=25258662|pmc=4172669|volume=6|year=2014|journal=World J Stem Cells|pages=404–20}}</ref>||[[United States]]
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|1960–1969||Discovery||Various studies show that the drug [[wikipedia:Cytarabine|cytarabine (ara-C)]] has activity against leukemias and provides a major boost to combination chemotherapy for [[wikipedia:acute myeloid leukemia|acute myeloid leukemia]].<ref name="timeline" />||  
 
|-
 
|-
|1958||Discovery||Scientists find that a combination of the drugs [[Mercaptopurine|6-mercaptopurine]] and [[methotrexate]] can reduce or eliminate cancer growth and extend survival in patients with leukemia. It is discovered that carefully honed drug combinations can attack cancer cells from different angles.<ref name="timeline" />||[[United States]]
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|1960||Discovery||Researchers identify a chromosomal abnormality linked to many leukemias. A decade later, it is discovered that this abnormality results when parts of chromosomes 9 and 22 switch places in a phenomenon called [[wikipedia:Chromosomal translocation|translocation]].<ref name="timeline" />||[[wikipedia:Philadelphia|Philadelphia]], [[wikipedia:United States|United States]]
 
|-
 
|-
|1960–1969||Discovery||Various studies show that the drug [[Cytarabine|cytarabine (ara-C)]] has activity against leukemias and provides a major boost to combination chemotherapy for [[acute myeloid leukemia]].<ref name="timeline" />||  
+
|1961||Discovery||Researchers demonstrate that drug [[wikipedia:vinblastine|vinblastine]] blocks a key protein involved in cancer cell division and induces some leukemias and lymphomas into remission. Vinblastine is approved by the [[wikipedia:FDA|FDA]].<ref name="timeline" />||[[wikipedia:United States|United States]]
 
|-
 
|-
|1960||Discovery||Researchers identify a chromosomal abnormality linked to many leukemias. A decade later, it is discovered that this abnormality results when parts of chromosomes 9 and 22 switch places in a phenomenon called [[Chromosomal translocation|translocation]].<ref name="timeline" />||[[Philadelphia]], [[United States]]
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|1963||Development||[[wikipedia:Vincristine|Vincristine]], a sister drug to [[wikipedia:vinblastine|vinblastine]], is approved by the [[wikipedia:FDA|FDA]].<ref name="timeline" />||[[wikipedia:United States|United States]]  
 
|-
 
|-
|1961||Discovery||Researchers demonstrate that drug [[vinblastine]] blocks a key protein involved in cancer cell division and induces some leukemias and lymphomas into remission. Vinblastine is approved by the [[FDA]].<ref name="timeline" />||[[United States]]
+
|1965||Organization||The [[wikipedia:International Agency for Research on Cancer|International Agency for Research on Cancer]] (IARC) is founded as an intergovernmental agency forming part of the [[wikipedia:World Health Organization|World Health Organization]] of the [[wikipedia:United Nations|United Nations]]. Its role is to conduct and coordinate research into the causes of cancer.<ref>{{cite web|title=IARC|url=http://apps.who.int/bookorders/anglais/detart1.jsp?codlan=1&codcol=76&codcch=34|accessdate=21 November 2016}}</ref>||[[wikipedia:Lyon|Lyon]], [[wikipedia:France|France]]
 
|-
 
|-
|1963||Development||[[Vincristine]], a sister drug to [[vinblastine]], is approved by the [[FDA]].<ref name="timeline" />||[[United States]]  
+
|1974||Development||[[wikipedia:Antibiotic|Antibiotic]] [[wikipedia:doxorubicin|doxorubicin]] is approved by the [[wikipedia:FDA|FDA]] to treat many cancer types, including some leukemias. Together with [[wikipedia:cytarabine|cytarabine]], doxorubicin induces [[wikipedia:acute myeloid leukemia|acute myeloid leukemia]] remissions by damaging the [[wikipedia:DNA|DNA]] of [[wikipedia:cancer cells|cancer cells]].<ref name="timeline" />||[[wikipedia:United States|United States]]  
 
|-
 
|-
|1965||Organization||The [[International Agency for Research on Cancer]] (IARC) is founded as an intergovernmental agency forming part of the [[World Health Organization]] of the [[United Nations]]. Its role is to conduct and coordinate research into the causes of cancer.<ref>{{cite web|title=IARC|url=http://apps.who.int/bookorders/anglais/detart1.jsp?codlan=1&codcol=76&codcch=34|accessdate=21 November 2016}}</ref>||[[Lyon]], [[France]]
+
|1977||Discovery||Chemotherapy drug [[wikipedia:chlorambucil|chlorambucil]] is found to slow the progression of chronic [[wikipedia:lymphocytic leukemia|lymphocytic leukemia]], the second most common type of leukemia in adults.<ref name="timeline" />||
 
|-
 
|-
|1974||Development||[[Antibiotic]] [[doxorubicin]] is approved by the [[FDA]] to treat many cancer types, including some leukemias. Together with [[cytarabine]], doxorubicin induces [[acute myeloid leukemia]] remissions by damaging the [[DNA]] of [[cancer cells]].<ref name="timeline" />||[[United States]]
+
|1980||Discovery||Human T-cell leukemia virus [[wikipedia:Human T-lymphotropic virus|type 1 (HTLV-I)]] is identified. It is the first virus that causes cancer being discovered.<ref>{{cite journal|title=Human T-cell leukemia virus type I (HTLV-I) infection and the onset of adult T-cell leukemia (ATL)|doi=10.1186/1742-4690-2-27| pmid=15854229|pmc=1131926|volume=2|year=2005|journal=Retrovirology|pages=27 | last1 = Matsuoka | first1 = M}}</ref><ref>{{cite web|title=Fifty Years of Milestones in Cancer Research|url=http://www.webmd.com/prostate-cancer/features/fifty-years-of-milestones-in-cancer-research?page=2|accessdate=28 August 2016}}</ref>||  
 
|-
 
|-
|1977||Discovery||Chemotherapy drug [[chlorambucil]] is found to slow the progression of chronic [[lymphocytic leukemia]], the second most common type of leukemia in adults.<ref name="timeline" />||
+
|1982||Discovery||A large trial shows that using the [[wikipedia:anthracycline|anthracycline]] [[wikipedia:daunorubicin|daunorubicin]], in combination with [[wikipedia:cytarabine|cytarabine]], is more effective at causing complete remissions of [[wikipedia:acute myeloid leukemia|acute myeloid leukemia]] than the previously-standard drug, [[wikipedia:doxorubicin|doxorubicin]].<ref name="timeline" />||
 
|-
 
|-
|1980||Discovery||Human T-cell leukemia virus [[Human T-lymphotropic virus|type 1 (HTLV-I)]] is identified. It is the first virus that causes cancer being discovered.<ref>{{cite journal|title=Human T-cell leukemia virus type I (HTLV-I) infection and the onset of adult T-cell leukemia (ATL)|doi=10.1186/1742-4690-2-27| pmid=15854229|pmc=1131926|volume=2|year=2005|journal=Retrovirology|pages=27 | last1 = Matsuoka | first1 = M}}</ref><ref>{{cite web|title=Fifty Years of Milestones in Cancer Research|url=http://www.webmd.com/prostate-cancer/features/fifty-years-of-milestones-in-cancer-research?page=2|accessdate=28 August 2016}}</ref>||  
+
|1986||Organization||The [[wikipedia:National Marrow Donor Program|National Marrow Donor Program]] is established as a nonprofit organization. It operates the world's largest registry of unrelated adult donors and umbilical [[wikipedia:cord blood|cord blood]] units, which contain [[wikipedia:stem cell|stem cell]]s that can help save the lives of some patients with blood-related cancers.<ref name="timeline" />||[[wikipedia:St. Paul|St. Paul]], [[wikipedia:Minnesota|Minnesota]], [[wikipedia:United States|United States]]
 
|-
 
|-
|1982||Discovery||A large trial shows that using the [[anthracycline]] [[daunorubicin]], in combination with [[cytarabine]], is more effective at causing complete remissions of [[acute myeloid leukemia]] than the previously-standard drug, [[doxorubicin]].<ref name="timeline" />||
+
|1986–1989||Discovery||Scientists find that occupational exposure to [[wikipedia:benzene|benzene]] is associated with increased risk of developing [[wikipedia:non-lymphocytic leukemia|non-lymphocytic leukemia]], [[wikipedia:non-Hodgkin lymphoma|non-Hodgkin lymphoma]], and other diseases.<ref name="timeline" />||  
 
|-
 
|-
|1986||Organization||The [[National Marrow Donor Program]] is established as a nonprofit organization. It operates the world's largest registry of unrelated adult donors and umbilical [[cord blood]] units, which contain [[stem cell]]s that can help save the lives of some patients with blood-related cancers.<ref name="timeline" />||[[St. Paul]], [[Minnesota]], [[United States]]  
+
|1988||Organization||The [[wikipedia:José Carreras Leukaemia Foundation|José Carreras Leukaemia Foundation]] is founded by tenor [[wikipedia:José Carreras|José Carreras]]. It finances national and international scientific research projects, among other activities.<ref>{{cite web|title=José Carreras foundation|url=https://www.mariinsky.ru/en/company/opera_guest/jose_carreras/|accessdate=19 August 2016}}</ref>||[[wikipedia:Barcelona|Barcelona]], [[wikipedia:Spain|Spain]] (branches in [[wikipedia:United States|United States]], [[wikipedia:Switzerland|Switzerland]] and [[wikipedia:Germany|Germany]])
 
|-
 
|-
|1986–1989||Discovery||Scientists find that occupational exposure to [[benzene]] is associated with increased risk of developing [[non-lymphocytic leukemia]], [[non-Hodgkin lymphoma]], and other diseases.<ref name="timeline" />||  
+
|1989||Organization||[[wikipedia:The Simon Flavell Leukaemia Research Laboratory|The Simon Flavell Leukaemia Research Laboratory]] is founded. It aims at supporting children and adults who have been diagnosed with leukemia and [[wikipedia:lymphoma|lymphoma]], and conducting research programmes into new antibody-based treatments.<ref>{{cite web|title=David Flavell|url=https://www.ljmu.ac.uk/about-us/fellows/honorary-fellows-2013/david-flavell|accessdate=19 August 2016}}</ref><ref>{{cite web|title=Simon Flavell Leukaemia Research Laboratory  research|url=http://www.telegraph.co.uk/news/health/news/7648847/Common-flower-could-revolutionise-treatment-of-leukemia.html|accessdate=19 August 2016}}</ref>||[[wikipedia:Southampton|Southampton]], United Kingdom
 
|-
 
|-
|1988||Organization||The [[José Carreras Leukaemia Foundation]] is founded by tenor [[José Carreras]]. It finances national and international scientific research projects, among other activities.<ref>{{cite web|title=José Carreras foundation|url=https://www.mariinsky.ru/en/company/opera_guest/jose_carreras/|accessdate=19 August 2016}}</ref>||[[Barcelona]], [[Spain]] (branches in [[United States]], [[Switzerland]] and [[Germany]])
+
|1990–1994||Development||[[wikipedia:Fludarabine|Fludarabine]] is introduced, and proven effective for patients who do not respond to [[wikipedia:chlorambucil|chlorambucil]] for treating leukemia.<ref name="timeline" /><ref>{{cite journal|title=Fludarabine Compared with Chlorambucil as Primary Therapy for Chronic Lymphocytic Leukemia|doi=10.1056/NEJM200012143432402|url=http://www.nejm.org/doi/full/10.1056/NEJM200012143432402#Background=&t=abstract | volume=343|journal=New England Journal of Medicine|pages=1750–1757|pmid=11114313|date=December 2000 | last1 = Rai | first1 = KR | last2 = Peterson | first2 = BL | last3 = Appelbaum | first3 = FR | display-authors = 3 | last4 = et al}}</ref>||
 
|-
 
|-
|1989||Organization||[[The Simon Flavell Leukaemia Research Laboratory]] is founded. It aims at supporting children and adults who have been diagnosed with leukemia and [[lymphoma]], and conducting research programmes into new antibody-based treatments.<ref>{{cite web|title=David Flavell|url=https://www.ljmu.ac.uk/about-us/fellows/honorary-fellows-2013/david-flavell|accessdate=19 August 2016}}</ref><ref>{{cite web|title=Simon Flavell Leukaemia Research Laboratory  research|url=http://www.telegraph.co.uk/news/health/news/7648847/Common-flower-could-revolutionise-treatment-of-leukemia.html|accessdate=19 August 2016}}</ref>||[[Southampton]], United Kingdom
+
|1993||Treatment||[[wikipedia:Stem cell|Stem cell]] transplantation for treating leukemia is performed for the first time.<ref>{{cite journal|title=Haploidentical stem cell transplantation for acute leukemia.|pmid=12430847 | volume=76 Suppl 1 | journal=Int J Hematol|pages=165–8 | last1 = Aversa | first1 = F | last2 = Terenzi | first2 = A | last3 = Felicini | first3 = R | last4 = Carotti | first4 = A | last5 = Falcinelli | first5 = F | last6 = Tabilio | first6 = A | last7 = Velardi | first7 = A | last8 = Martelli | first8 = MF | doi=10.1007/bf03165238}}</ref><ref>{{cite web|title=Fifty Years of Milestones in Cancer Research|url=http://www.webmd.com/prostate-cancer/features/fifty-years-of-milestones-in-cancer-research?page=3|accessdate=28 August 2016}}</ref>||
 
|-
 
|-
|1990–1994||Development||[[Fludarabine]] is introduced, and proven effective for patients who do not respond to [[chlorambucil]] for treating leukemia.<ref name="timeline" /><ref>{{cite journal|title=Fludarabine Compared with Chlorambucil as Primary Therapy for Chronic Lymphocytic Leukemia|doi=10.1056/NEJM200012143432402|url=http://www.nejm.org/doi/full/10.1056/NEJM200012143432402#Background=&t=abstract | volume=343|journal=New England Journal of Medicine|pages=1750–1757|pmid=11114313|date=December 2000 | last1 = Rai | first1 = KR | last2 = Peterson | first2 = BL | last3 = Appelbaum | first3 = FR | display-authors = 3 | last4 = et al}}</ref>||
+
|1995||Discovery||Researchers discover that Lymphocyte transfusions from a biologically matched, healthy donor to a patient with chronic [[wikipedia:myeloid leukemia|myeloid leukemia]] can help drive the leukemia back into remission if the cancer returns after a previous stem cell or bone marrow transplant from the same donor.<ref name="timeline" />||
 
|-
 
|-
|1993||Treatment||[[Stem cell]] transplantation for treating leukemia is performed for the first time.<ref>{{cite journal|title=Haploidentical stem cell transplantation for acute leukemia.|pmid=12430847 | volume=76 Suppl 1 | journal=Int J Hematol|pages=165–8 | last1 = Aversa | first1 = F | last2 = Terenzi | first2 = A | last3 = Felicini | first3 = R | last4 = Carotti | first4 = A | last5 = Falcinelli | first5 = F | last6 = Tabilio | first6 = A | last7 = Velardi | first7 = A | last8 = Martelli | first8 = MF | doi=10.1007/bf03165238}}</ref><ref>{{cite web|title=Fifty Years of Milestones in Cancer Research|url=http://www.webmd.com/prostate-cancer/features/fifty-years-of-milestones-in-cancer-research?page=3|accessdate=28 August 2016}}</ref>||
+
|1995||Discovery||[[wikipedia:Tretinoin|Tretinoin]] is found to cause remission in patients with [[wikipedia:acute promyelocytic leukemia|acute promyelocytic leukemia]].<ref name="timeline" />||  
 
|-
 
|-
|1995||Discovery||Researchers discover that Lymphocyte transfusions from a biologically matched, healthy donor to a patient with chronic [[myeloid leukemia]] can help drive the leukemia back into remission if the cancer returns after a previous stem cell or bone marrow transplant from the same donor.<ref name="timeline" />||
+
|2000||Discovery||Large clinical trial demonstrates that drug [[wikipedia:fludarabine|fludarabine]], which was originally developed as a back-up therapy for patients with [[wikipedia:B-cell chronic lymphocytic leukemia|chronic lymphocytic leukemia]], works in more patients and produces longer lasting remissions than previous standard drug, [[wikipedia:chlorambucil|chlorambucil]].<ref name="timeline" />||  
 
|-
 
|-
|1995||Discovery||[[Tretinoin]] is found to cause remission in patients with [[acute promyelocytic leukemia]].<ref name="timeline" />||  
+
|2001|| Treatment ||The [[wikipedia:FDA|FDA]] approves [[wikipedia:imatinib|imatinib]] after the drug is shown to halt the growth of [[wikipedia:chronic myelogenous leukemia|chronic myelogenous leukemia]] in the majority of patients.<ref name="timeline" />||[[wikipedia:United States|United States]]
 
|-
 
|-
|2000||Discovery||Large clinical trial demonstrates that drug [[fludarabine]], which was originally developed as a back-up therapy for patients with [[B-cell chronic lymphocytic leukemia|chronic lymphocytic leukemia]], works in more patients and produces longer lasting remissions than previous standard drug, [[chlorambucil]].<ref name="timeline" />||  
+
|2004–2006||Development||Epigenetic drugs [[wikipedia:azacytidine|azacytidine]] and [[wikipedia:decitabine|decitabine]] are approved by the FDA to prevent cancer in patients with [[wikipedia:myelodysplastic syndrome|myelodysplastic syndrome]]s, a group of blood disorders that predispose a person to [[wikipedia:acute myelogenous leukemia|acute myelogenous leukemia]].<ref name="timeline" />||[[wikipedia:United States|United States]]
 
|-
 
|-
|2001||Discovery||The [[FDA]] approves [[imatinib]] after the drug is shown to halt the growth of [[chronic myelogenous leukemia]] in the majority of patients.<ref name="timeline" />||[[United States]]
+
|2005|| Treatment ||FDA approves [[wikipedia:palifermin|palifermin]] to reduce oral sores associated with chemotherapy in patients with blood cancers.<ref name="timeline" />||
 
|-
 
|-
|2004–2006||Development||Epigenetic drugs [[azacytidine]] and [[decitabine]] are approved by the FDA to prevent cancer in patients with [[myelodysplastic syndrome]]s, a group of blood disorders that predispose a person to [[acute myelogenous leukemia]].<ref name="timeline" />||[[United States]]
+
|2006||Discovery||[[wikipedia:Dasatinib|Dasatinib]] is found to help as second targeted treatment for patients with [[wikipedia:chronic myelogenous leukemia|chronic myelogenous leukemia]] who cannot tolerate or develop resistance to [[wikipedia:imatinib|imatinib]].<ref name="timeline" />||  
 
|-
 
|-
|2005||Development||FDA approves [[palifermin]] to reduce oral sores associated with chemotherapy in patients with blood cancers.<ref name="timeline" />||
+
|2008||Development||[[wikipedia:Acute Myeloid Leukemia|Acute Myeloid Leukemia]] becomes the first cancer genome to be fully sequenced.  [[wikipedia:DNA|DNA]] is extracted from leukemic cells and compared to unaffected skin. Acquired mutations in several genes that have not previously been associated with the disease are found in leukemic cells.<ref name="Acute Myeloid Leukemia History">{{cite web|title=Acute Myeloid Leukemia History|url=http://www.news-medical.net/health/Acute-Myeloid-Leukemia-History.aspx|accessdate=17 August 2016}}</ref>||
 
|-
 
|-
|2006||Discovery||[[Dasatinib]] is found to help as second targeted treatment for patients with [[chronic myelogenous leukemia]] who cannot tolerate or develop resistance to [[imatinib]].<ref name="timeline" />||  
+
| 2011 || Discovery || A large trial establishes that progression of [[wikipedia:B-cell chronic lymphocytic leukemia|chronic lymphocytic leukemia]] slows and survival improves after adding targeted drug [[wikipedia:rituximab|rituximab]] to initial treatment with standard drug [[wikipedia:fludarabine|fludarabine]].<ref name="timeline" />||
 
|-
 
|-
|2008||Development||[[Acute Myeloid Leukemia]] becomes the first cancer genome to be fully sequenced.  [[DNA]] is extracted from leukemic cells and compared to unaffected skin. Acquired mutations in several genes that have not previously been associated with the disease are found in leukemic cells.<ref name="Acute Myeloid Leukemia History">{{cite web|title=Acute Myeloid Leukemia History|url=http://www.news-medical.net/health/Acute-Myeloid-Leukemia-History.aspx|accessdate=17 August 2016}}</ref>||
+
| 2017 || Treatment || The United States {{w|Food and Drug Administration}} approves the first gene therapy, {{w|tisagenlecleucel}} (Kymriah), for refractory B-cell precursor acute lymphoblastic leukemia.<ref>{{cite web |title=The Past and Future of Gene Therapy |url=https://www.specialtypharmacytimes.com/news/the-past-and-future-of-gene-therapy |website=specialtypharmacytimes.com |accessdate=18 October 2018}}</ref> || {{w|United States}}
 
|-
 
|-
|2011||Discovery||A large trial establishes that progression of [[B-cell chronic lymphocytic leukemia|chronic lymphocytic leukemia]] slows and survival improves after adding targeted drug [[rituximab]] to initial treatment with standard drug [[fludarabine]].<ref name="timeline" />||
 
 
|}
 
|}
  
 
==See also==
 
==See also==
* [[Timeline of melanoma]]
+
 
* [[Timeline of lymphoma]]
+
* [[wikipedia:Timeline of melanoma|Timeline of melanoma]]
* [[Timeline of lung cancer]]
+
* [[wikipedia:Timeline of lymphoma|Timeline of lymphoma]]
* [[Timeline of brain cancer]]
+
* [[wikipedia:Timeline of lung cancer|Timeline of lung cancer]]
 +
* [[wikipedia:Timeline of brain cancer|Timeline of brain cancer]]
  
 
==References==
 
==References==
 
{{Reflist}}
 
{{Reflist}}
 
{{Cancer timeline}}
 
{{Cancer timeline}}
[[Category:Leukemia]]
+
[[wikipedia:Category:Leukemia|Category:Leukemia]]
[[Category:Health-related timelines]]
+
[[wikipedia:Category:Health-related timelines|Category:Health-related timelines]]
[[Category:Medicine timelines]]
+
[[wikipedia:Category:Medicine timelines|Category:Medicine timelines]]

Revision as of 22:58, 29 March 2021

The content on this page is forked from the English Wikipedia page entitled "Timeline of leukemia". The original page still exists at Timeline of leukemia. The original content was released under the Creative Commons Attribution/Share-Alike License (CC-BY-SA), so this page inherits this license.

This is a timeline of leukemia, describing especially major discoveries and advances in treatment against the disease.

Big picture

Year/period Key developments
Prior to 1800 Various cancers, including leukemia, are described in ancient Egyptian texts dating back to 3000 BC. Translations inform "large, protruding mass" or "thick blood" and describe the disease as "there is no treatment." This basic understanding of leukemia and cancer lasts for millennia.[1]
19th Century Discovery of leukemia. Velpeau (1825), Donné (1844), Bennett (1845), Craigie (1845), Virchow (1845), and Fuller (1846), establish the possibility that sustained leukocytosis could occur in the absence of infection. The term leukemia is adopted to describe such conditions.[2][3][4] It is discovered that leukemia originates in the bone marrow. Histologic stains for microscopic study are introduced.[2]
1900s Leukemia is subdivided in four primary types: acute myeloid leukemia, chronic myeloid leukemia, acute lymphocytic leukemia and chronic lymphocytic leukemia.[5][6]
1940s–present Era of chemotherapy development, also the first effective leukemia treatments with drugs introduced by Sidney Farber.[3][7][8] Childhood leukemia is thought to be on a constant rise in the 20th and 21st century.[9] In 2010, globally, approximately 281,500 people died of leukemia.[10] In 2000, approximately 256,000 children and adults around the world developed a form of leukemia, and 209,000 died from it.[11] DNA and genetic analysis have opened a new chapter in leukemia treatments.[9]

Visual data

Evolution of new leukemia cases and deaths per 100,000 people in the United States for the period 1975-2013, according to the National Cancer Institute. Age-adjusted.[12]

Google Trends

The comparative chart below shows Google Trends data Leukemia (Syndrome) and Leukemia (Search Term), from January 2004 to March 2021, when the screenshot was taken. Interest is also ranked by country and displayed on world map.[13]

Leukemia gt.png

Google Ngram Viewer

The chart below shows Google Ngram Viewer data for Leukemia, from 1500 to 2019.[14]

Leukemia ngram.png

Wikipedia Views

The chart below shows pageviews of the English Wikipedia article Leukemia, on desktop from December 2007, and on mobile-web, desktop-spider, mobile-web-spider and mobile app, from July 2015; to February 2021.[15]

Leukemia wv.png


Full timeline

Year/period Type of event Event Location
1749 Discovery French physician Joseph Lieutaud first notes white cells, calling them globuli albicantes.[16]
1774 Development English surgeon William Hewson publishes work on the lymphatic system and first describes the lymphocyte.[16] United Kingdom
1811 Development Peter Cullen defines a case of splenitis acutus with unexplainable milky blood.[17] Edinburgh, Scotland
1825 Development French surgeon Alfred Velpeau defines the leukemia associated symptoms, and observes pus in the blood vessels.[17]
1844 Discovery French bacteriologist Alfred Donné detects a maturation arrest of the white blood cells.[17]
1845 Development English physician John Bennett renames splenitis acutus to leucocythemia, based on the microscopic accumulation of purulent leukocytes.[17][18]
1845–1847 Development German physician Rudolf Virchow defines a reversed white and red blood cell balance. Virchow introduces the term leukemia for the disease (leukämie in German).[2][17]
1868 Discovery German pathologist Ernst Neumann reports changes in the bone marrow in leukaemia and establishes the link between the source of blood and the bone marrow.[3] Königsberg, Prussia
1877 Medical development Swiss pathologist Paul Ehrlich develops methods for staining tissue, making possible to distinguish between different types of blood cells, thus leading to the capability to diagnose numerous blood diseases.[2][3][4] Germany
1879 Medical development F. Mosler first describes the technique of bone marrow examination to diagnose leukemia.[4]
1889 Development German physician Wilhelm Ebstein introduces the term acute leukemia to differentiate rapidly progressive and fatal leukemias from the more indolent chronic leukemias.[4] Prussia
1900 Development Swiss hematologist Otto Naegeli refines the classification of leukemia by dividing it into myelogenous and lymphocytic classes.[2][3][4]
1936 Medical development American hematologist John H. Lawrence of the University of California, Berkeley introduces phosphorus-32 for the treatment of leukemia.[19][20][21] United States
1946 Organization Leukemia Research Foundation is established. It is dedicated to combating all blood cancers by funding research.[22] Northfield, Illinois, United States
1947 Discovery American pediatric pathologist Sidney Farber discovers that aminopterin can induce remissions in acute lymphocytic leukemia in children, leading to the development of a new category of chemotherapy drugs, called antimetabolites, that impair the ability of cancer cells to grow and replicate. It is considered the first effective leukemia treatment.[8]
1949 Organization Leukemia & Lymphoma Society is founded. It is the world's largest voluntary health organization dedicated to funding blood cancer research, education and patient services.[23][24] Rye Brook, New York (serves the United States and Canada)
1949–1956 Discovery Researchers discover ways to protect the body from radiation damage by shielding a mouse's spleen from radiation. Eventually, it is learned that the body recruits stem cells, which are found in the spleen and bone marrow, to protect and heal itself from radiation damage.[8]
1957 Development Researchers report the first bone marrow transplantation for treating leukemia, although with poor results. It would not be until the late 1970s when marrow transplantation becomes successful due to tissue matching.[25] United States
1958 Discovery Scientists find that a combination of the drugs 6-mercaptopurine and methotrexate can reduce or eliminate cancer growth and extend survival in patients with leukemia. It is discovered that carefully honed drug combinations can attack cancer cells from different angles.[8] United States
1960–1969 Discovery Various studies show that the drug cytarabine (ara-C) has activity against leukemias and provides a major boost to combination chemotherapy for acute myeloid leukemia.[8]
1960 Discovery Researchers identify a chromosomal abnormality linked to many leukemias. A decade later, it is discovered that this abnormality results when parts of chromosomes 9 and 22 switch places in a phenomenon called translocation.[8] Philadelphia, United States
1961 Discovery Researchers demonstrate that drug vinblastine blocks a key protein involved in cancer cell division and induces some leukemias and lymphomas into remission. Vinblastine is approved by the FDA.[8] United States
1963 Development Vincristine, a sister drug to vinblastine, is approved by the FDA.[8] United States
1965 Organization The International Agency for Research on Cancer (IARC) is founded as an intergovernmental agency forming part of the World Health Organization of the United Nations. Its role is to conduct and coordinate research into the causes of cancer.[26] Lyon, France
1974 Development Antibiotic doxorubicin is approved by the FDA to treat many cancer types, including some leukemias. Together with cytarabine, doxorubicin induces acute myeloid leukemia remissions by damaging the DNA of cancer cells.[8] United States
1977 Discovery Chemotherapy drug chlorambucil is found to slow the progression of chronic lymphocytic leukemia, the second most common type of leukemia in adults.[8]
1980 Discovery Human T-cell leukemia virus type 1 (HTLV-I) is identified. It is the first virus that causes cancer being discovered.[27][28]
1982 Discovery A large trial shows that using the anthracycline daunorubicin, in combination with cytarabine, is more effective at causing complete remissions of acute myeloid leukemia than the previously-standard drug, doxorubicin.[8]
1986 Organization The National Marrow Donor Program is established as a nonprofit organization. It operates the world's largest registry of unrelated adult donors and umbilical cord blood units, which contain stem cells that can help save the lives of some patients with blood-related cancers.[8] St. Paul, Minnesota, United States
1986–1989 Discovery Scientists find that occupational exposure to benzene is associated with increased risk of developing non-lymphocytic leukemia, non-Hodgkin lymphoma, and other diseases.[8]
1988 Organization The José Carreras Leukaemia Foundation is founded by tenor José Carreras. It finances national and international scientific research projects, among other activities.[29] Barcelona, Spain (branches in United States, Switzerland and Germany)
1989 Organization The Simon Flavell Leukaemia Research Laboratory is founded. It aims at supporting children and adults who have been diagnosed with leukemia and lymphoma, and conducting research programmes into new antibody-based treatments.[30][31] Southampton, United Kingdom
1990–1994 Development Fludarabine is introduced, and proven effective for patients who do not respond to chlorambucil for treating leukemia.[8][32]
1993 Treatment Stem cell transplantation for treating leukemia is performed for the first time.[33][34]
1995 Discovery Researchers discover that Lymphocyte transfusions from a biologically matched, healthy donor to a patient with chronic myeloid leukemia can help drive the leukemia back into remission if the cancer returns after a previous stem cell or bone marrow transplant from the same donor.[8]
1995 Discovery Tretinoin is found to cause remission in patients with acute promyelocytic leukemia.[8]
2000 Discovery Large clinical trial demonstrates that drug fludarabine, which was originally developed as a back-up therapy for patients with chronic lymphocytic leukemia, works in more patients and produces longer lasting remissions than previous standard drug, chlorambucil.[8]
2001 Treatment The FDA approves imatinib after the drug is shown to halt the growth of chronic myelogenous leukemia in the majority of patients.[8] United States
2004–2006 Development Epigenetic drugs azacytidine and decitabine are approved by the FDA to prevent cancer in patients with myelodysplastic syndromes, a group of blood disorders that predispose a person to acute myelogenous leukemia.[8] United States
2005 Treatment FDA approves palifermin to reduce oral sores associated with chemotherapy in patients with blood cancers.[8]
2006 Discovery Dasatinib is found to help as second targeted treatment for patients with chronic myelogenous leukemia who cannot tolerate or develop resistance to imatinib.[8]
2008 Development Acute Myeloid Leukemia becomes the first cancer genome to be fully sequenced. DNA is extracted from leukemic cells and compared to unaffected skin. Acquired mutations in several genes that have not previously been associated with the disease are found in leukemic cells.[4]
2011 Discovery A large trial establishes that progression of chronic lymphocytic leukemia slows and survival improves after adding targeted drug rituximab to initial treatment with standard drug fludarabine.[8]
2017 Treatment The United States Food and Drug Administration approves the first gene therapy, tisagenlecleucel (Kymriah), for refractory B-cell precursor acute lymphoblastic leukemia.[35] United States

See also

References

  1. "History of Leukemia". Retrieved 20 August 2016. 
  2. 2.0 2.1 2.2 2.3 2.4 "The leukemias". Retrieved 17 August 2016. 
  3. 3.0 3.1 3.2 3.3 3.4 "Leukaemia – a brief historical review from ancient times to 1950". Retrieved 17 August 2016. 
  4. 4.0 4.1 4.2 4.3 4.4 4.5 "Acute Myeloid Leukemia History". Retrieved 17 August 2016. 
  5. "Leukemia types". Retrieved 18 August 2016. 
  6. "La historia de la leucemia". Retrieved 18 August 2016. 
  7. "Sidney Farber". Retrieved 18 August 2016. 
  8. 8.00 8.01 8.02 8.03 8.04 8.05 8.06 8.07 8.08 8.09 8.10 8.11 8.12 8.13 8.14 8.15 8.16 8.17 8.18 8.19 8.20 8.21 "Leukemia Progress & Timeline". Retrieved 16 August 2016. 
  9. 9.0 9.1 "History of leukemia". Retrieved 19 August 2016. 
  10. "Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010". Lancet. 380 (9859): 2095–128. December 2012. PMID 23245604. doi:10.1016/S0140-6736(12)61728-0. 
  11. Mathers, Colin D, Cynthia Boschi-Pinto, Alan D Lopez and Christopher JL Murray (2001). "Cancer incidence, mortality and survival by site for 14 regions of the world" (PDF). Global Programme on Evidence for Health Policy Discussion Paper No. 13. World Health Organization. 
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Category:Leukemia Category:Health-related timelines Category:Medicine timelines