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男性乳腺癌患者中细胞周期蛋白依赖性激酶 4-6(CDK 4-6)抑制剂的临床结局:一项多中心研究。

Clinical outcomes of cyclin-dependent kinase 4-6 (CDK 4-6) inhibitors in patients with male breast cancer: A multicenter study.

机构信息

Hacettepe University Faculty of Medicine, Department of Medical Oncology, Ankara, Turkey.

Erciyes University Faculty of Medicine, Department of Medical Oncology, Kayseri, Turkey.

出版信息

Breast. 2022 Dec;66:85-88. doi: 10.1016/j.breast.2022.09.009. Epub 2022 Sep 30.

DOI:10.1016/j.breast.2022.09.009
PMID:36208540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9547301/
Abstract

BACKGROUND

Since breast cancer is less common in men than in women, data on the use of new therapeutic agents, including cyclin-dependent kinase 4-6 (CDK 4-6) inhibitors, are limited in patients with metastatic hormone receptor positive (HR+), human epidermal growth factor receptor 2-negative (HER2-) male breast cancer. Therefore; we aimed to investigate the treatment responses of metastatic HR+, HER2-male breast cancer patients treated with CDK 4-6 inhibitors in a multicenter real-life cohort.

METHODS

Male patients with a diagnosis of HR+ and HER2-metastatic breast cancer, treated with any CDK 4-6 inhibitor, were included in the study. Demographic and clinical characteristics of the patients were recorded. We aimed to determine progression-free survival (PFS) time, response rates and drug related side effects.

RESULTS

A total 25 patients from 14 institutions were recruited. The mean age at diagnosis was 57 years. Median follow-up was 19.53 (95% CI: 14.04-25.02) months. The overall response rate was 60%. While the median PFS was 20.6 months in the whole cohort, it wasn't reached in those using CDK 4-6 inhibitors in first line and 10 months in the subsequent lines (p:0.009). No new adverse events were encountered.

CONCLUSION

In our study, we found that CDK 4-6 inhibitors are effective and safe options in men with HR+ and HER2-metastatic breast cancer as in women. Our results support the use of CDK 4-6 inhibitor-based combinations in the first-line treatment of HR+ and HER2-metastatic male breast cancer.

摘要

背景

由于男性乳腺癌的发病率低于女性,因此转移性激素受体阳性(HR+)、人表皮生长因子受体 2 阴性(HER2-)男性乳腺癌患者使用新型治疗药物的数据(包括细胞周期蛋白依赖性激酶 4-6(CDK 4-6)抑制剂)有限。因此;我们旨在调查 CDK 4-6 抑制剂治疗转移性 HR+、HER2-男性乳腺癌患者的治疗反应在多中心真实世界队列中。

方法

本研究纳入了诊断为 HR+和 HER2-转移性乳腺癌且接受任何 CDK 4-6 抑制剂治疗的男性患者。记录了患者的人口统计学和临床特征。我们旨在确定无进展生存期(PFS)时间、反应率和药物相关副作用。

结果

共招募了来自 14 个机构的 25 名患者。诊断时的平均年龄为 57 岁。中位随访时间为 19.53 个月(95%CI:14.04-25.02)。总缓解率为 60%。虽然整个队列的中位 PFS 为 20.6 个月,但在一线使用 CDK 4-6 抑制剂的患者中未达到,在后续线中为 10 个月(p:0.009)。未发现新的不良事件。

结论

在我们的研究中,我们发现 CDK 4-6 抑制剂在 HR+和 HER2-转移性男性乳腺癌患者中与女性一样是有效且安全的选择。我们的结果支持在 HR+和 HER2-转移性男性乳腺癌的一线治疗中使用 CDK 4-6 抑制剂为基础的联合治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83ae/9547301/8194d7d402c6/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83ae/9547301/8194d7d402c6/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83ae/9547301/8194d7d402c6/gr1.jpg

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