Department of Radiological, Oncological and Pathological Sciences, Sapienza-University of Rome, 00161 Rome, Italy.
Institut Jules Bordet and l'Université Libre de Bruxelles (U.L.B.), Hôpital Universitaire de Bruxelles (HUB), Rue Meylemeersch, 90 (Rez Haut Nord), Anderlecht, 1070 Brussels, Belgium; Department of Internal Medicine and Medical Specialties (DIMI), School of Medicine, University of Genova, Genova, Italy.
Cancer Treat Rev. 2024 Jul;128:102769. doi: 10.1016/j.ctrv.2024.102769. Epub 2024 May 22.
The therapeutic landscape for early breast cancer (eBC) has expanded by introducing novel anticancer agents into clinical practice. During their reproductive years, women with eBC should be informed of the potential risk of premature ovarian insufficiency (POI) and infertility with the proposed systemic therapy. Although the topic of female fertility is becoming increasingly relevant in patients with cancer, limited information is available on the gonadotoxicity of new agents available for eBC treatment. Analyses from clinical trials and prospective data on ovarian function biomarkers are lacking. The purpose of this systematic review is to report the available preclinical and clinical data on female fertility risk with the use of the new agents that are part of clinical practice use or under development for eBC management. This review highlights the clear need to perform additional research efforts to improve our understanding on the gonoadtoxicity of new anticancer agents.
早期乳腺癌(eBC)的治疗领域通过将新型抗癌药物引入临床实践而得到了扩展。患有 eBC 的女性在其生育年龄段时,应被告知拟议的系统治疗可能导致卵巢早衰(POI)和不孕的潜在风险。尽管癌症患者的女性生育能力问题越来越受到关注,但关于新型 eBC 治疗药物的性腺毒性的信息有限。缺乏关于卵巢功能生物标志物的临床试验分析和前瞻性数据。本系统评价的目的是报告使用新的治疗药物的临床前和临床数据,这些药物是临床实践中使用的一部分或正在开发用于 eBC 管理。本综述强调了明确需要进行额外的研究工作,以提高我们对新型抗癌药物的性腺毒性的理解。