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Defining AML and MDS second cancer risk dynamics after diagnoses of first cancers treated or not with radiation
Risks of acute myeloid leukemia (AML) and/or myelodysplastic syndromes (MDS) are known to increase after cancer treatments. Their rise-and-fall dynamics and their associations with radiation have, however, not been fully characterized. To improve risk definition we developed SEERaBomb R software for...
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Published in: | Leukemia 2016-02, Vol.30 (2), p.285-294 |
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description | Risks of acute myeloid leukemia (AML) and/or myelodysplastic syndromes (MDS) are known to increase after cancer treatments. Their rise-and-fall dynamics and their associations with radiation have, however, not been fully characterized. To improve risk definition we developed SEERaBomb R software for Surveillance, Epidemiology and End Results second cancer analyses. Resulting high-resolution relative risk (RR) time courses were compared, where possible, to results of A-bomb survivor analyses. We found: (1) persons with prostate cancer receiving radiation therapy have increased RR of AML and MDS that peak in 1.5–2.5 years; (2) persons with non-Hodgkin lymphoma (NHL), lung and breast first cancers have the highest RR for AML and MDS over the next 1–12 years. These increased RR are radiation specific for lung and breast cancer but not for NHL; (3) AML latencies were brief compared to those of A-bomb survivors; and (4) there was a marked excess risk of acute promyelocytic leukemia in persons receiving radiation therapy. Knowing the type of first cancer, if it was treated with radiation, the interval from first cancer diagnosis to developing AML or MDS, and the type of AML, can improve estimates of whether AML or MDS cases developing in this setting are due to background versus other processes. |
doi_str_mv | 10.1038/leu.2015.258 |
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Their rise-and-fall dynamics and their associations with radiation have, however, not been fully characterized. To improve risk definition we developed SEERaBomb R software for Surveillance, Epidemiology and End Results second cancer analyses. Resulting high-resolution relative risk (RR) time courses were compared, where possible, to results of A-bomb survivor analyses. We found: (1) persons with prostate cancer receiving radiation therapy have increased RR of AML and MDS that peak in 1.5–2.5 years; (2) persons with non-Hodgkin lymphoma (NHL), lung and breast first cancers have the highest RR for AML and MDS over the next 1–12 years. These increased RR are radiation specific for lung and breast cancer but not for NHL; (3) AML latencies were brief compared to those of A-bomb survivors; and (4) there was a marked excess risk of acute promyelocytic leukemia in persons receiving radiation therapy. Knowing the type of first cancer, if it was treated with radiation, the interval from first cancer diagnosis to developing AML or MDS, and the type of AML, can improve estimates of whether AML or MDS cases developing in this setting are due to background versus other processes.</description><identifier>ISSN: 0887-6924</identifier><identifier>EISSN: 1476-5551</identifier><identifier>DOI: 10.1038/leu.2015.258</identifier><identifier>PMID: 26460209</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/67/1990/1673 ; 631/67/1990/283/1897 ; 631/67/2324 ; 692/308/174 ; 692/499 ; Acute myeloid leukemia ; Acute promyeloid leukemia ; Breast cancer ; Cancer ; Cancer Research ; Cancer therapies ; Care and treatment ; Complications and side effects ; Critical Care Medicine ; Disease susceptibility ; Epidemiology ; Female ; Health risks ; Hematology ; Humans ; Intensive ; Internal Medicine ; Leukemia ; Leukemia, Myeloid, Acute - etiology ; Lung cancer ; Lungs ; Lymphoma ; Male ; Medical diagnosis ; Medicine ; Medicine & Public Health ; Methods ; Myelodysplastic syndrome ; Myelodysplastic syndromes ; Myelodysplastic Syndromes - etiology ; Neoplasms - radiotherapy ; Neoplasms, Second Primary - etiology ; Non-Hodgkin's lymphoma ; Oncology ; Oncology, Experimental ; original-article ; Patient outcomes ; Promyeloid leukemia ; Prostate cancer ; Radiation ; Radiation therapy ; Radiotherapy ; Radiotherapy - adverse effects ; Risk ; Risk factors ; Second primary cancer</subject><ispartof>Leukemia, 2016-02, Vol.30 (2), p.285-294</ispartof><rights>Macmillan Publishers Limited 2016</rights><rights>COPYRIGHT 2016 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Feb 2016</rights><rights>Macmillan Publishers Limited 2016.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c684t-2f0dd6407a513f1751703748a2e9f2da1530b8418fcf8b10158552c93c8c8963</citedby><cites>FETCH-LOGICAL-c684t-2f0dd6407a513f1751703748a2e9f2da1530b8418fcf8b10158552c93c8c8963</cites><orcidid>0000-0002-9701-1851</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26460209$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Radivoyevitch, T</creatorcontrib><creatorcontrib>Sachs, R K</creatorcontrib><creatorcontrib>Gale, R P</creatorcontrib><creatorcontrib>Molenaar, R J</creatorcontrib><creatorcontrib>Brenner, D J</creatorcontrib><creatorcontrib>Hill, B T</creatorcontrib><creatorcontrib>Kalaycio, M E</creatorcontrib><creatorcontrib>Carraway, H E</creatorcontrib><creatorcontrib>Mukherjee, S</creatorcontrib><creatorcontrib>Sekeres, M A</creatorcontrib><creatorcontrib>Maciejewski, J P</creatorcontrib><title>Defining AML and MDS second cancer risk dynamics after diagnoses of first cancers treated or not with radiation</title><title>Leukemia</title><addtitle>Leukemia</addtitle><addtitle>Leukemia</addtitle><description>Risks of acute myeloid leukemia (AML) and/or myelodysplastic syndromes (MDS) are known to increase after cancer treatments. 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Academic</collection><jtitle>Leukemia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Radivoyevitch, T</au><au>Sachs, R K</au><au>Gale, R P</au><au>Molenaar, R J</au><au>Brenner, D J</au><au>Hill, B T</au><au>Kalaycio, M E</au><au>Carraway, H E</au><au>Mukherjee, S</au><au>Sekeres, M A</au><au>Maciejewski, J P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Defining AML and MDS second cancer risk dynamics after diagnoses of first cancers treated or not with radiation</atitle><jtitle>Leukemia</jtitle><stitle>Leukemia</stitle><addtitle>Leukemia</addtitle><date>2016-02-01</date><risdate>2016</risdate><volume>30</volume><issue>2</issue><spage>285</spage><epage>294</epage><pages>285-294</pages><issn>0887-6924</issn><eissn>1476-5551</eissn><abstract>Risks of acute myeloid leukemia (AML) and/or myelodysplastic syndromes (MDS) are known to increase after cancer treatments. Their rise-and-fall dynamics and their associations with radiation have, however, not been fully characterized. To improve risk definition we developed SEERaBomb R software for Surveillance, Epidemiology and End Results second cancer analyses. Resulting high-resolution relative risk (RR) time courses were compared, where possible, to results of A-bomb survivor analyses. We found: (1) persons with prostate cancer receiving radiation therapy have increased RR of AML and MDS that peak in 1.5–2.5 years; (2) persons with non-Hodgkin lymphoma (NHL), lung and breast first cancers have the highest RR for AML and MDS over the next 1–12 years. These increased RR are radiation specific for lung and breast cancer but not for NHL; (3) AML latencies were brief compared to those of A-bomb survivors; and (4) there was a marked excess risk of acute promyelocytic leukemia in persons receiving radiation therapy. Knowing the type of first cancer, if it was treated with radiation, the interval from first cancer diagnosis to developing AML or MDS, and the type of AML, can improve estimates of whether AML or MDS cases developing in this setting are due to background versus other processes.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26460209</pmid><doi>10.1038/leu.2015.258</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-9701-1851</orcidid></addata></record> |
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subjects | 631/67/1990/1673 631/67/1990/283/1897 631/67/2324 692/308/174 692/499 Acute myeloid leukemia Acute promyeloid leukemia Breast cancer Cancer Cancer Research Cancer therapies Care and treatment Complications and side effects Critical Care Medicine Disease susceptibility Epidemiology Female Health risks Hematology Humans Intensive Internal Medicine Leukemia Leukemia, Myeloid, Acute - etiology Lung cancer Lungs Lymphoma Male Medical diagnosis Medicine Medicine & Public Health Methods Myelodysplastic syndrome Myelodysplastic syndromes Myelodysplastic Syndromes - etiology Neoplasms - radiotherapy Neoplasms, Second Primary - etiology Non-Hodgkin's lymphoma Oncology Oncology, Experimental original-article Patient outcomes Promyeloid leukemia Prostate cancer Radiation Radiation therapy Radiotherapy Radiotherapy - adverse effects Risk Risk factors Second primary cancer |
title | Defining AML and MDS second cancer risk dynamics after diagnoses of first cancers treated or not with radiation |
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