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哌柏西利联合内分泌治疗用于日本HR+/HER2-晚期乳腺癌患者一线或二线治疗的总生存期:一项多中心观察性研究(P-BRIDGE研究)

Overall survival of palbociclib plus endocrine therapy in Japanese patients with HR+/HER2- advanced breast cancer in the first-or second-line setting: a multicenter observational study (P-BRIDGE study).

作者信息

Nagai Shigenori E, Hattori Masaya, Yoshinami Tetsuhiro, Masuda Hiroko, Okamura Takuho, Watanabe Kenichi, Nakayama Takahiro, Tsuneizumi Michiko, Takabatake Daisuke, Harao Michiko, Yoshino Hiroshi, Mori Natsuko, Yasojima Hiroyuki, Oshiro Chiya, Iwase Madoka, Yamaguchi Miki, Sangai Takafumi, Sasada Shinsuke, Ishida Takanori, Futamura Manabu, Muramatsu Yasuaki, Kosaka Nobuyoshi, Masuda Norikazu

机构信息

Division of Breast Oncology, Saitama Prefectural Cancer Center, Saitama, Japan.

Department of Breast Oncology, Aichi Cancer Center, Nagoya, Japan.

出版信息

Breast Cancer. 2025 Apr 5. doi: 10.1007/s12282-025-01689-4.

Abstract

BACKGROUND

Recently, we reported the real-world effectiveness of palbociclib plus endocrine therapy (ET) in HR+/HER2- advanced breast cancer (ABC) in Japan (NCT05399329). However, median overall survival (OS) was not reached because of limited follow-up (36 months). Here, we present follow-up data from this study, including real-world clinical outcomes and treatment patterns.

METHODS

The P-BRIDGE study was a multi-center, observational study evaluating the real-world effectiveness and treatment patterns of patients diagnosed with HR+/HER2- ABC who received palbociclib plus ET in first (1L) or second line (2L) in Japan. The primary endpoint was real-world progression-free survival (rwPFS); secondary endpoints included OS and chemotherapy-free survival (CFS).

RESULTS

Of the 693 eligible patients, 426 and 267 patients received palbociclib with ET as 1L and 2L treatment, respectively. After a median follow-up of 48.1 months, the median rwPFS (95% CI) was 26.2 months (21.4-30.4) for 1L and 14.9 months (11.7-18.3) for 2L, respectively. Median OS (95% CI) was 68.2 months (60.8-NE) for 1L and 50.7 months (42.2-57.2) for 2L, respectively. OS analysis was also performed in the following subgroups: TFI < 12 months/TFI ≥ 12months/de novo metastatic median OS was 56.3 months (43.9-68.2), NR (NE-NE), NR (56.3-NE), visceral metastasis was 65.0 months (56.3-NE), liver metastasis was 46.4 months (37.2-NE), and bone only metastasis was NR (57.8-NE) in 1L, respectively.

CONCLUSIONS

The updated results from this study further confirm the real-world effectiveness of palbociclib plus ET in routine clinical practice in Japan. More than 5 years of median OS in 1L was observed, supporting the use of palbociclib plus ET as 1L standard of care for HR+/HER2- ABC.

摘要

背景

最近,我们报道了哌柏西利联合内分泌治疗(ET)在日本激素受体阳性/人表皮生长因子受体2阴性晚期乳腺癌(ABC)中的真实世界疗效(NCT05399329)。然而,由于随访时间有限(36个月),未达到中位总生存期(OS)。在此,我们展示了这项研究的随访数据,包括真实世界的临床结局和治疗模式。

方法

P-BRIDGE研究是一项多中心观察性研究,评估在日本一线(1L)或二线(2L)接受哌柏西利联合ET治疗的激素受体阳性/人表皮生长因子受体2阴性ABC患者的真实世界疗效和治疗模式。主要终点是真实世界无进展生存期(rwPFS);次要终点包括总生存期(OS)和无化疗生存期(CFS)。

结果

在693例符合条件的患者中,分别有426例和267例患者接受哌柏西利联合ET作为1L和2L治疗。中位随访48.1个月后,1L的中位rwPFS(95%CI)为26.2个月(21.4 - 30.4),2L为14.9个月(11.7 - 18.3)。1L的中位OS(95%CI)为68.2个月(60.8 - NE),2L为50.7个月(42.2 - 57.2)。还在以下亚组中进行了OS分析:无病间期(TFI)<12个月/TFI≥12个月/初发转移,1L的中位OS分别为56.3个月(43.9 - 68.2)、未达到(NE - NE)、未达到(56.3 - NE),内脏转移为65.0个月(56.3 - NE),肝转移为46.4个月(37.2 - NE),仅骨转移未达到(未达到 - NE)。

结论

本研究的更新结果进一步证实了哌柏西利联合ET在日本常规临床实践中的真实世界疗效。观察到1L的中位OS超过5年,支持将哌柏西利联合ET作为激素受体阳性/人表皮生长因子受体2阴性ABC的1L标准治疗方案。

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