女性乳腺癌后第二次非乳房原发的风险:系统回顾和荟萃分析。

Isaac Allen, Hend Hassan, Eleni Sofianopoulou, Diana Eccles, Clare Turnbull, Marc Tischkowitz, Paul Pharoah, Antonis C Antoniou
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引用次数: 0

摘要

背景:乳腺癌幸存者的第二原发癌发病率正在上升。通过系统回顾和荟萃分析,我们检查了非乳房二次原发的风险,结合特定的癌症部位。方法:我们对PubMed、Embase和Web of Science进行了系统搜索,寻找2022年3月之前发表的研究。我们纳入了报告标准化发病率(SIRs)及相关标准误差的研究,以评估乳腺癌后第二次非乳房原发的综合风险。我们根据年龄、随访时间和地理区域对合并的第二主要风险进行了荟萃分析。我们还评估了几个特定部位的第二主要风险,按年龄分层。所有meta分析均采用dersimonan - laird估计量的方差逆方法,假设为随机效应模型。使用纽卡斯尔-渥太华量表评估相关偏差和研究质量。结果:1项前瞻性研究和27项回顾性队列研究被确定。第二次非乳房原发的SIRs为0.84 ~ 1.84。总SIR估计为1.24 (95% CI 1.14-1.36, I2: 99%)。这因年龄而异:50岁之前诊断乳腺癌的估计为1.59 (95% CI 1.36-1.85),显著高于50岁或以上首次诊断乳腺癌的女性(SIR: 1.13, 95% CI 1.01-1.36, p为差异)。结论:乳腺癌幸存者在许多部位发生第二次原发的风险显著增加。与欧洲乳腺癌幸存者相比,50岁之前被诊断为乳腺癌的人和亚洲乳腺癌幸存者的风险更高。由于缺乏潜在混杂变量的数据,本研究受到限制。结论可能为乳腺癌后的临床管理决策提供信息,尽管具体的临床建议不在本综述的范围内。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Risks of second non-breast primaries following breast cancer in women: a systematic review and meta-analysis.

Risks of second non-breast primaries following breast cancer in women: a systematic review and meta-analysis.

Risks of second non-breast primaries following breast cancer in women: a systematic review and meta-analysis.

Risks of second non-breast primaries following breast cancer in women: a systematic review and meta-analysis.

Background: Second primary cancer incidence is rising among breast cancer survivors. We examined the risks of non-breast second primaries, in combination and at specific cancer sites, through a systematic review and meta-analysis.

Methods: We conducted a systematic search of PubMed, Embase, and Web of Science, seeking studies published by March 2022. We included studies that reported standardized incidence ratios (SIRs), with associated standard errors, assessing the combined risk of second non-breast primaries following breast cancer. We performed meta-analyses of combined second primary risks, stratifying by age, follow-up duration, and geographic region. We also assessed second primary risks at several specific sites, stratifying by age. The inverse variance method with DerSimonian-Laird estimators was used in all meta-analyses, assuming a random-effects model. Associated biases and study quality were evaluated using the Newcastle-Ottawa scale.

Results: One prospective and twenty-seven retrospective cohort studies were identified. SIRs for second non-breast primaries combined ranged from 0.84 to 1.84. The summary SIR estimate was 1.24 (95% CI 1.14-1.36, I2: 99%). This varied by age: the estimate was 1.59 (95% CI 1.36-1.85) when breast cancer was diagnosed before age 50, which was significantly higher than in women first diagnosed at 50 or over (SIR: 1.13, 95% CI 1.01-1.36, p for difference: < 0.001). SPC risks were also significantly higher when based on Asian, rather than European, registries (Asia-SIR: 1.47, 95% CI 1.29-1.67. Europe-SIR: 1.16, 95% CI 1.04-1.28). There were significantly increased risks of second thyroid (SIR: 1.89, 95% CI 1.49-2.38), corpus uteri (SIR: 1.84, 95% CI 1.53-2.23), ovary (SIR: 1.53, 95% CI 1.35-1.73), kidney (SIR: 1.43, 95% CI 1.17-1.73), oesophagus (SIR: 1.39, 95% CI 1.26-1.55), skin (melanoma) (SIR: 1.34, 95% CI 1.18-1.52), blood (leukaemia) (SIR: 1.30, 95% CI 1.17-1.45), lung (SIR: 1.25, 95% CI 1.03-1.51), stomach (SIR: 1.23, 95% CI 1.12-1.36) and bladder (SIR: 1.15, 95% CI 1.05-1.26) primaries.

Conclusions: Breast cancer survivors are at significantly increased risk of second primaries at many sites. Risks are higher for those diagnosed with breast cancer before age 50 and in Asian breast cancer survivors compared to European breast cancer survivors. This study is limited by a lack of data on potentially confounding variables. The conclusions may inform clinical management decisions following breast cancer, although specific clinical recommendations lie outside the scope of this review.

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