Department of Clinical Epidemiology, Department of Clinical Medicine, Aarhus University Hospital & Aarhus University, Aarhus, Denmark.
Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Breast Cancer Res Treat. 2023 Nov;202(1):11-22. doi: 10.1007/s10549-023-07043-6. Epub 2023 Sep 1.
Breast cancer and its treatments may increase the risk of type 2 diabetes (T2D). We conducted a systematic review and meta-analysis to investigate the association between breast cancer and the incidence of T2D overall, and according to breast cancer treatments.
We searched PubMed, Embase and references of relevant papers for studies on breast cancer, breast cancer treatment, and subsequent T2D risk. Using random-effects models, we calculated effect estimates and associated 95% confidence intervals of the association between breast cancer, adjuvant breast cancer treatments (i.e., endocrine therapy (tamoxifen, aromatase inhibitors, and combined) and chemotherapy), and subsequent T2D. We used funnel plots to assess publication bias.
Among 15 eligible studies, 10 reported on T2D risk after breast cancer, chemotherapy, or endocrine therapy; five studies investigated more than one association. Compared with patients without breast cancer, those with breast cancer and those who received any endocrine therapy had elevated risk of incident T2D (EE = 1.23, 95% CI = 1.13-1.33 and EE = 1.23, 95% CI = 1.16-1.32, respectively). Among breast cancer patients only, the risk of T2D was higher for those who received tamoxifen compared with those who did not receive tamoxifen (EE = 1.28, 95% CI = 1.18-1.38). Due to few studies, analyses investigating T2D risk after treatment with aromatase inhibitors or chemotherapy were inconclusive.
Our findings suggest an elevated risk of T2D in breast cancer survivors, particularly after tamoxifen therapy. Further research is needed to determine the impact of aromatase inhibitors, and chemotherapy on the incidence of T2D after breast cancer.
乳腺癌及其治疗可能会增加 2 型糖尿病(T2D)的风险。我们进行了一项系统评价和荟萃分析,以调查乳腺癌与 T2D 总体发病风险之间的关系,以及根据乳腺癌的治疗方法进行的调查。
我们在 PubMed、Embase 和相关文献的参考文献中搜索了关于乳腺癌、乳腺癌治疗和随后发生 T2D 风险的研究。我们使用随机效应模型计算了乳腺癌、辅助乳腺癌治疗(即内分泌治疗(他莫昔芬、芳香化酶抑制剂和联合)和化疗)与随后发生 T2D 之间关联的效应估计值和相关的 95%置信区间。我们使用漏斗图评估了发表偏倚。
在 15 项合格的研究中,有 10 项报告了乳腺癌、化疗或内分泌治疗后 T2D 的发病风险;有 5 项研究调查了多种关联。与没有乳腺癌的患者相比,患有乳腺癌和接受任何内分泌治疗的患者发生 T2D 的风险增加(EE=1.23,95%CI=1.13-1.33 和 EE=1.23,95%CI=1.16-1.32)。仅在乳腺癌患者中,接受他莫昔芬治疗的患者发生 T2D 的风险高于未接受他莫昔芬治疗的患者(EE=1.28,95%CI=1.18-1.38)。由于研究较少,分析乳腺癌患者接受芳香化酶抑制剂或化疗后 T2D 发病风险的结果尚无定论。
我们的研究结果表明,乳腺癌幸存者 T2D 的风险升高,特别是在接受他莫昔芬治疗后。需要进一步的研究来确定芳香化酶抑制剂和化疗对乳腺癌后 T2D 发生率的影响。