کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3444196 1595250 2014 4 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Age-specific incidence of all neoplasms after colorectal cancer
ترجمه فارسی عنوان
بروز بیماری خاصی در تمام موارد نئوپلاسم بعد از سرطان کولورکتال
کلمات کلیدی
سرطان روده بزرگ، چندین بدخیمی، رجیستر سرطان، وقوع
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی پزشکی و دندانپزشکی (عمومی)
چکیده انگلیسی

PurposePatients diagnosed with a specific neoplasm tend to have a subsequent excess risk of the same neoplasm. The age incidence of a second neoplasm at the same site is approximately constant with age, and consequently the relative risk is greater at younger age. It is unclear whether such a line of reasoning can be extended from a specific neoplasm to the incidence of all neoplasms in subjects diagnosed with a defined neoplasm.MethodsWe considered the age-specific incidence of all non–hormone-related epithelial neoplasms after a first primary colorectal cancer (n = 9542) in the Vaud Cancer Registry data set.ResultsIn subjects with a previous colorectal cancer, the incidence rate of all other epithelial non–hormone-related cancers was stable around 800 per 100,000 between age 30 and 60 years, and rose only about twofold to reach 1685 at age 70 to 79 years and 1826 per 100,000 at age 80 years or older. After excluding synchronous cancers, the rise was only about 1.5-fold, that is, from about 700 to 1000. In the general population, the incidence rate of all epithelial non–hormone-related cancers was 29 per 100,000 at age 30 to 39 years, and rose 30-fold to 883 per 100,000 at age 70 to 79 years. Excluding colorectal cancers, the rise of all non–hormone-related cancers was from 360 per 100,000 at age 40 to 49 years to 940 at age 70 to 79 years after colorectal cancer, and from 90 to 636 per 100,000 in the general population (i.e., 2.6- vs. 7.1-fold).ConclusionsThe rise of incidence with age of all epithelial non–hormone-related second cancers after colorectal cancer is much smaller than in the general population. This can possibly be related to the occurrence of a single mutational event in a population of susceptible individuals, although alternative models are plausible within the complexity of the process of carcinogenesis.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Annals of Epidemiology - Volume 24, Issue 10, October 2014, Pages 785–788
نویسندگان
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