Cancer Survivorship—Genetic Susceptibility and Second Primary Cancers: Research Strategies and Recommendations
Cancer survivors constitute 3.5% of the United States population, but second primary malignancies among this high-risk group now account for 16% of all cancer incidence. Although few data currently exist regarding the molecular mechanisms for second primary cancers and other late outcomes after canc...
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creator | Travis, Lois B. Rabkin, Charles S. Brown, Linda Morris Allan, James M. Alter, Blanche P. Ambrosone, Christine B. Begg, Colin B. Caporaso, Neil Chanock, Stephen DeMichele, Angela Figg, William Douglas Gospodarowicz, Mary K. Hall, Eric J. Hisada, Michie Inskip, Peter Kleinerman, Ruth Little, John B. Malkin, David Ng, Andrea K. Offit, Kenneth Pui, Ching-Hon Robison, Leslie L. Rothman, Nathaniel Shields, Peter G. Strong, Louise Taniguchi, Toshiyasu Tucker, Margaret A. Greene, Mark H. |
description | Cancer survivors constitute 3.5% of the United States population, but second primary malignancies among this high-risk group now account for 16% of all cancer incidence. Although few data currently exist regarding the molecular mechanisms for second primary cancers and other late outcomes after cancer treatment, the careful measurement and documentation of potentially carcinogenic treatments (chemotherapy and radiotherapy) provide a unique platform for in vivo research on gene–environment interactions in human carcinogenesis. We review research priorities identified during a National Cancer Institute (NCI)–sponsored workshop entitled “Cancer Survivorship—Genetic Susceptibility and Second Primary Cancers.” These priorities include 1) development of a national research infrastructure for studies of cancer survivorship; 2) creation of a coordinated system for biospecimen collection; 3) development of new technology, bioinformatics, and biomarkers; 4) design of new epidemiologic methods; and 5) development of evidence-based clinical practice guidelines. Many of the infrastructure resources and design strategies that would facilitate research in this area also provide a foundation for the study of other important nonneoplastic late effects of treatment and psychosocial concerns among cancer survivors. These research areas warrant high priority to promote NCI's goal of eliminating pain and suffering related to cancer. |
doi_str_mv | 10.1093/jnci/djj001 |
format | Article |
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Although few data currently exist regarding the molecular mechanisms for second primary cancers and other late outcomes after cancer treatment, the careful measurement and documentation of potentially carcinogenic treatments (chemotherapy and radiotherapy) provide a unique platform for in vivo research on gene–environment interactions in human carcinogenesis. We review research priorities identified during a National Cancer Institute (NCI)–sponsored workshop entitled “Cancer Survivorship—Genetic Susceptibility and Second Primary Cancers.” These priorities include 1) development of a national research infrastructure for studies of cancer survivorship; 2) creation of a coordinated system for biospecimen collection; 3) development of new technology, bioinformatics, and biomarkers; 4) design of new epidemiologic methods; and 5) development of evidence-based clinical practice guidelines. Many of the infrastructure resources and design strategies that would facilitate research in this area also provide a foundation for the study of other important nonneoplastic late effects of treatment and psychosocial concerns among cancer survivors. These research areas warrant high priority to promote NCI's goal of eliminating pain and suffering related to cancer.</description><identifier>ISSN: 0027-8874</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/djj001</identifier><identifier>PMID: 16391368</identifier><identifier>CODEN: JNCIEQ</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Antineoplastic Agents - adverse effects ; Biotechnology ; Cancer ; Carcinogens ; Case-Control Studies ; Chemotherapy ; Clinical trials ; Clinical Trials as Topic ; Cohort Studies ; Congresses as Topic ; Genes ; Genetic Predisposition to Disease ; Humans ; Medical Informatics ; Medical research ; Medical treatment ; Multicenter Studies as Topic ; Neoplasms - drug therapy ; Neoplasms - genetics ; Neoplasms - mortality ; Neoplasms - radiotherapy ; Neoplasms, Radiation-Induced - chemically induced ; Neoplasms, Radiation-Induced - etiology ; Neoplasms, Radiation-Induced - genetics ; Neoplasms, Second Primary - chemically induced ; Neoplasms, Second Primary - etiology ; Neoplasms, Second Primary - genetics ; Radiotherapy - adverse effects ; Registries ; Specimen Handling ; Survivor ; Survivors - statistics & numerical data ; Syndrome ; United States - epidemiology</subject><ispartof>JNCI : Journal of the National Cancer Institute, 2006-01, Vol.98 (1), p.15-25</ispartof><rights>Copyright Oxford University Press(England) Jan 4, 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c449t-5358985bec4efd218a6ca7704df655cbe72605233505674313af39d1db78eee73</citedby><cites>FETCH-LOGICAL-c449t-5358985bec4efd218a6ca7704df655cbe72605233505674313af39d1db78eee73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16391368$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Travis, Lois B.</creatorcontrib><creatorcontrib>Rabkin, Charles S.</creatorcontrib><creatorcontrib>Brown, Linda Morris</creatorcontrib><creatorcontrib>Allan, James M.</creatorcontrib><creatorcontrib>Alter, Blanche P.</creatorcontrib><creatorcontrib>Ambrosone, Christine B.</creatorcontrib><creatorcontrib>Begg, Colin B.</creatorcontrib><creatorcontrib>Caporaso, Neil</creatorcontrib><creatorcontrib>Chanock, Stephen</creatorcontrib><creatorcontrib>DeMichele, Angela</creatorcontrib><creatorcontrib>Figg, William Douglas</creatorcontrib><creatorcontrib>Gospodarowicz, Mary K.</creatorcontrib><creatorcontrib>Hall, Eric J.</creatorcontrib><creatorcontrib>Hisada, Michie</creatorcontrib><creatorcontrib>Inskip, Peter</creatorcontrib><creatorcontrib>Kleinerman, Ruth</creatorcontrib><creatorcontrib>Little, John B.</creatorcontrib><creatorcontrib>Malkin, David</creatorcontrib><creatorcontrib>Ng, Andrea K.</creatorcontrib><creatorcontrib>Offit, Kenneth</creatorcontrib><creatorcontrib>Pui, Ching-Hon</creatorcontrib><creatorcontrib>Robison, Leslie L.</creatorcontrib><creatorcontrib>Rothman, Nathaniel</creatorcontrib><creatorcontrib>Shields, Peter G.</creatorcontrib><creatorcontrib>Strong, Louise</creatorcontrib><creatorcontrib>Taniguchi, Toshiyasu</creatorcontrib><creatorcontrib>Tucker, Margaret A.</creatorcontrib><creatorcontrib>Greene, Mark H.</creatorcontrib><title>Cancer Survivorship—Genetic Susceptibility and Second Primary Cancers: Research Strategies and Recommendations</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>JNCI J Natl Cancer Inst</addtitle><description>Cancer survivors constitute 3.5% of the United States population, but second primary malignancies among this high-risk group now account for 16% of all cancer incidence. Although few data currently exist regarding the molecular mechanisms for second primary cancers and other late outcomes after cancer treatment, the careful measurement and documentation of potentially carcinogenic treatments (chemotherapy and radiotherapy) provide a unique platform for in vivo research on gene–environment interactions in human carcinogenesis. We review research priorities identified during a National Cancer Institute (NCI)–sponsored workshop entitled “Cancer Survivorship—Genetic Susceptibility and Second Primary Cancers.” These priorities include 1) development of a national research infrastructure for studies of cancer survivorship; 2) creation of a coordinated system for biospecimen collection; 3) development of new technology, bioinformatics, and biomarkers; 4) design of new epidemiologic methods; and 5) development of evidence-based clinical practice guidelines. Many of the infrastructure resources and design strategies that would facilitate research in this area also provide a foundation for the study of other important nonneoplastic late effects of treatment and psychosocial concerns among cancer survivors. These research areas warrant high priority to promote NCI's goal of eliminating pain and suffering related to cancer.</description><subject>Antineoplastic Agents - adverse effects</subject><subject>Biotechnology</subject><subject>Cancer</subject><subject>Carcinogens</subject><subject>Case-Control Studies</subject><subject>Chemotherapy</subject><subject>Clinical trials</subject><subject>Clinical Trials as Topic</subject><subject>Cohort Studies</subject><subject>Congresses as Topic</subject><subject>Genes</subject><subject>Genetic Predisposition to Disease</subject><subject>Humans</subject><subject>Medical Informatics</subject><subject>Medical research</subject><subject>Medical treatment</subject><subject>Multicenter Studies as Topic</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - genetics</subject><subject>Neoplasms - mortality</subject><subject>Neoplasms - radiotherapy</subject><subject>Neoplasms, Radiation-Induced - chemically induced</subject><subject>Neoplasms, Radiation-Induced - 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Although few data currently exist regarding the molecular mechanisms for second primary cancers and other late outcomes after cancer treatment, the careful measurement and documentation of potentially carcinogenic treatments (chemotherapy and radiotherapy) provide a unique platform for in vivo research on gene–environment interactions in human carcinogenesis. We review research priorities identified during a National Cancer Institute (NCI)–sponsored workshop entitled “Cancer Survivorship—Genetic Susceptibility and Second Primary Cancers.” These priorities include 1) development of a national research infrastructure for studies of cancer survivorship; 2) creation of a coordinated system for biospecimen collection; 3) development of new technology, bioinformatics, and biomarkers; 4) design of new epidemiologic methods; and 5) development of evidence-based clinical practice guidelines. Many of the infrastructure resources and design strategies that would facilitate research in this area also provide a foundation for the study of other important nonneoplastic late effects of treatment and psychosocial concerns among cancer survivors. These research areas warrant high priority to promote NCI's goal of eliminating pain and suffering related to cancer.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>16391368</pmid><doi>10.1093/jnci/djj001</doi><tpages>11</tpages></addata></record> |
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subjects | Antineoplastic Agents - adverse effects Biotechnology Cancer Carcinogens Case-Control Studies Chemotherapy Clinical trials Clinical Trials as Topic Cohort Studies Congresses as Topic Genes Genetic Predisposition to Disease Humans Medical Informatics Medical research Medical treatment Multicenter Studies as Topic Neoplasms - drug therapy Neoplasms - genetics Neoplasms - mortality Neoplasms - radiotherapy Neoplasms, Radiation-Induced - chemically induced Neoplasms, Radiation-Induced - etiology Neoplasms, Radiation-Induced - genetics Neoplasms, Second Primary - chemically induced Neoplasms, Second Primary - etiology Neoplasms, Second Primary - genetics Radiotherapy - adverse effects Registries Specimen Handling Survivor Survivors - statistics & numerical data Syndrome United States - epidemiology |
title | Cancer Survivorship—Genetic Susceptibility and Second Primary Cancers: Research Strategies and Recommendations |
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