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来自日本的真实世界证据,涉及接受CDK4/6抑制剂加内分泌治疗作为激素受体阳性、人表皮生长因子受体2阴性晚期或转移性乳腺癌一线或二线治疗的患者的生存结果和治疗顺序。

Real-world evidence from Japan regarding survival outcomes and treatment sequence in patients receiving CDK4/6 inhibitor plus endocrine therapy as first- or second-line treatment for hormone receptor-positive, HER2-negative advanced or metastatic breast cancer.

作者信息

Yoshinami Tetsuhiro, Takano Yuko, Ozaki Yukinori, Kajiwara Yukiko, Yamamoto Mitsugu, Watanabe Ken-Ichi, Tsukabe Masami, Fujisawa Fumie, Nagai Shigenori E, Shibata Nobuhiro, Oshiro Chiya, Bando Hiroko, Tsunoda Nobuyuki, Yamagami Kazuhiko, Koizumi Kei, Takada Masahiro, Toriguchi Naoko, Sekine Nobuyuki, Kawaguchi Tsutomu, Saji Shigehira, Sagara Yasuaki, Morita Satoshi, Masuda Norikazu

机构信息

Department of Breast and Endocrine Surgery, Graduate School of Medicine, Osaka University, 2-2-E10 Yamadaoka, Suita, Osaka, 565-0871, Japan.

Department of Breast and Endocrine Surgery, Nagoya University Hospital, Nagoya, Aichi, Japan.

出版信息

Breast Cancer. 2025 May 20. doi: 10.1007/s12282-025-01713-7.

Abstract

BACKGROUND

A cyclin-dependent kinase 4/6 inhibitor (CDK4/6i) plus endocrine therapy (ET) is a current standard first-/second-line treatment for hormone receptor (HR)-positive, HER2-negative advanced/metastatic breast cancer (AMBC). We aimed to provide real-world evidence regarding CDK4/6i therapy in this population.

METHODS

In this multicenter observational study, data from patients who had started CDK4/6i therapy between January 1, 2019, and December 31, 2021, as first-/second-line treatment for AMBC were used; real-world progression-free survival (rwPFS), chemotherapy-free survival, and overall survival were analyzed using the Kaplan-Meier method. Additionally, data were analyzed by separating patients with treatment-free interval (TFI) < 12 months (deemed resistant to ET) from the first-line treatment group (hereafter, the exclusive first-line treatment group).

RESULTS

Data from 745 patients were analyzed. Compared with palbociclib, abemaciclib was used in younger patients and those with expected poor prognosis. Median rwPFS was 36.8, 17.8, and 31.4 months in patients with de novo stage IV disease, TFI < 12 months, and TFI ≥ 12 months, respectively, in the first-line treatment group, and 17.4 months in the second-line treatment group. In the exclusive first-line treatment group, median rwPFS of the subsequent treatment after initial CDK4/6i plus ET was < 7 months, regardless of the type of subsequent treatment; prognosis was especially poor in those who were switched to chemotherapy.

CONCLUSIONS

The real-world survival outcomes found in this study for patients receiving first-/second-line CDK4/6i therapy were consistent with those of randomized phase 3 studies. As outcomes of subsequent treatment after initial CDK4/6i plus ET remain insufficient, further improvement in treatment is necessary.

摘要

背景

细胞周期蛋白依赖性激酶4/6抑制剂(CDK4/6i)联合内分泌治疗(ET)是目前激素受体(HR)阳性、人表皮生长因子受体2(HER2)阴性晚期/转移性乳腺癌(AMBC)的标准一线/二线治疗方案。我们旨在提供关于该人群CDK4/6i治疗的真实世界证据。

方法

在这项多中心观察性研究中,使用了2019年1月1日至2021年12月31日期间开始接受CDK4/6i治疗作为AMBC一线/二线治疗的患者数据;采用Kaplan-Meier方法分析真实世界无进展生存期(rwPFS)、无化疗生存期和总生存期。此外,将一线治疗组中无治疗间隔(TFI)<12个月(被认为对ET耐药)的患者(以下简称排他性一线治疗组)与其他患者分开进行数据分析。

结果

分析了745例患者的数据。与哌柏西利相比,阿贝西利用于更年轻的患者和预后预期较差的患者。在一线治疗组中,初治IV期疾病、TFI<12个月和TFI≥12个月的患者的中位rwPFS分别为36.8个月、17.8个月和31.4个月,二线治疗组为17.4个月。在排他性一线治疗组中,初始CDK4/6i联合ET治疗后后续治疗的中位rwPFS<7个月,无论后续治疗类型如何;改用化疗的患者预后尤其差。

结论

本研究中接受一线/二线CDK4/6i治疗的患者的真实世界生存结果与3期随机研究的结果一致。由于初始CDK4/6i联合ET治疗后后续治疗的结果仍然不足,有必要进一步改进治疗。

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