2007
DOI: 10.1200/jco.2006.09.0936
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Long-Term Solid Cancer Risk Among 5-Year Survivors of Hodgkin's Lymphoma

Abstract: Multivariable modeling demonstrates for the first time temporal changes in SC risk not evident in unadjusted analyses, and can facilitate the development of individualized risk assessment and the creation of screening strategies for early detection.

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Cited by 322 publications
(278 citation statements)
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“…4,7,[11][12][13][14] A protective effect of breastfeeding on the risk of premenopausal breast cancer has been observed in several studies, although not in all analyses. [31][32][33][34][35][36][37] Although the small size of this cohort prohibits analysis of the possibility that lactation might be protective, further studies in larger survivor cohorts may be indicated.…”
Section: Discussionmentioning
confidence: 99%
“…4,7,[11][12][13][14] A protective effect of breastfeeding on the risk of premenopausal breast cancer has been observed in several studies, although not in all analyses. [31][32][33][34][35][36][37] Although the small size of this cohort prohibits analysis of the possibility that lactation might be protective, further studies in larger survivor cohorts may be indicated.…”
Section: Discussionmentioning
confidence: 99%
“…8,9 Late effects, especially SPM and cardiovascular events, are well-known after first-line treatment of HL. [10][11][12][13][14][15][16] In contrast, only a few retrospective studies have addressed long-term effects after ASCT for relapsed or refractory HL. 17,18 Thus, long-term prospective data are lacking for first-relapsed or refractory HL treated with ASCT.…”
Section: A B D Cmentioning
confidence: 99%
“…[21] For instance, a risk model approximated that those diagnosed at the age of 30 with HL will have a 30 year cumulative risk of second primary malignancy for men and women at 18% and 26%, respectively, compared to age-matched risks of 7% and 9%. [22,23] The latency of the various second malignancies seen following therapy for HL varies by histology. Risk for myelodysplastic syndrome (MDS) and acute myelogenous leukemia (AML) peak at three to five years after therapy and return to population baseline, or at most remain minimally elevated, by 10 years after.…”
Section: Second Primary Malignancymentioning
confidence: 99%