Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2026
Risk Factors for Subsequent Primary Cancers in Colorectal Cancer Survivors: A Systematic Review and Meta-analysis.
Систематический обзорСтатьяМетаанализНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Aung Ye Kyaw, Zhang Ye, Baxter Nancy N, Jenkins Mark A, Win Aung Ko
Аннотация
As colorectal cancer survival improves, survivors face an increased risk of subsequent primary cancers (SPC). This systematic review assessed the associations between cancer treatments, tumor features, and other risk factors and the risk of SPCs for colorectal cancer survivors. We searched four databases for peer-reviewed articles published up to October 2025. We conducted meta-analyses using random-effects models to summarize pooled relative risks (RR) for each SPC. Of 10,577 articles screened, 36 met the inclusion criteria. Radiotherapy was associated with increased risks of uterine [RR, 2.65; 95% confidence interval (CI), 1.63-3.67], ovarian (RR, 2.26; 95% CI, 1.30-3.91), urethral (RR, 4.66; 95% CI, 1.96-11.06), and lung cancer (RR, 1.19; 95% CI, 1.04-1.35) but a decreased risk of prostate cancer (RR, 0.55; 95% CI, 0.47-0.64). In women, chemotherapy was associated with increased risks of uterine (RR, 2.26; 95% CI, 1.63-3.15) and breast cancer (RR, 1.22; 95% CI, 1.05-1.43). Colon (vs. rectal) and proximal colon (vs. distal) cancers were associated with higher SPC risk, whereas stage II/III (vs. stage I) was associated with lower SPC risk. Older age, male sex, White race (vs. Black/Asian), smoking, alcohol consumption, and metabolic comorbidities were associated with increased SPC risk. These findings support the need for risk-based surveillance after colorectal cancer.