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CDK4/6抑制剂治疗激素受体阳性、人表皮生长因子受体2阴性转移性乳腺癌患者的真实世界治疗结局:来自巴西一家参考中心的结果

Real-world treatment outcomes in HR+ HER2- metastatic breast cancer patients treated with CDK4/6 inhibitors: Results from a reference center in Brazil.

作者信息

Queiroz Marcello Moro, Sacardo Karina Perez, Ribeiro Mauricio Fernando, Gadotti Luiza Lara, Saddi Rodrigo, Oliveira Leandro Jonata de Carvalho, Linck Rudinei Diogo Marques, Cruz Marcelo Rocha de Souza, Barroso-Sousa Romualdo, Sahade Marina, Correa Tatiana Strava, Mano Max Senna, Suzuki Daniele Assad, Shimada Andrea Kazumi, Katz Artur

机构信息

Oncology Center, Hospital Sírio-Libanês, Street Dona Adma Jafet, number 115, zip-code 01308-050, São Paulo, SP, Brazil.

Oncology Center, DASA, Av. das Nações Unidas, number 7815, zip-code 05425-070, São Paulo, SP, Brazil.

出版信息

Cancer Treat Res Commun. 2023;35:100683. doi: 10.1016/j.ctarc.2023.100683. Epub 2023 Jan 19.

DOI:10.1016/j.ctarc.2023.100683
PMID:36716534
Abstract

BACKGROUND

Cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) have been recently developed and introduced into clinical practice.

METHODS

We retrospectively analyzed data from patients with confirmed HR+/HER2 metastatic breast cancer treated with hormonal therapy in combination with ribociclib (R), palbociclib (P), or abemaciclib (A).

OUTCOMES

median progression-free survival (mPFS), time to treatment discontinuation (mTTD), and objective response rate (ORR).

RESULTS

Between January 2016 - June 2021, 142 patients were treated with an CDK4/6i (79 P, 42 R, 21 A). The median age was 59 years and 67.6% had recurrent disease. Roughly 35.2%, 36.6%, 28.2% of the patients had 1, 2 or 3+ metastatic sites, respectively, and 55.6% of the patients received CDK4/6i as a first-line treatment. The mPFS was 28m(R) vs. 14m(P) vs. 6m(A) (P = 0.002), with a higher proportion of patients receiving R in the first-line setting. However, no difference was seen when the analysis was restricted to the first-line scenario (P = 0.193). Sixty-four patients required one dose reduction, and 19 patients required two. ORR was 76.2% (R) vs 62% (P) vs 42.9% (A). More patients achieved a complete response with R and P, with no difference in the incidence of partial response and stable disease. Adverse events occurred in 94.4% of the population, with the most common grade 3-4 AE being neutropenia (59.1%).

CONCLUSIONS

Our results confirm the efficacy and tolerability of CDK4/6i in routine clinical practice. This is the first real-world data describing and comparing the efficacy and toxicity of CDK4/6i in the Brazilian population.

摘要

背景

细胞周期蛋白依赖性激酶4/6抑制剂(CDK4/6i)最近已被开发并引入临床实践。

方法

我们回顾性分析了接受激素疗法联合瑞博西尼(R)、哌柏西利(P)或阿贝西利(A)治疗的确诊HR+/HER2转移性乳腺癌患者的数据。

结果

无进展生存期(mPFS)、治疗中断时间(mTTD)和客观缓解率(ORR)。

结果

2016年1月至2021年6月期间,142例患者接受了CDK4/6i治疗(79例接受P,42例接受R,21例接受A)。中位年龄为59岁,67.6%的患者患有复发性疾病。分别约35.2%、36.6%、28.2%的患者有1个、2个或3个以上转移部位,55.6%的患者接受CDK4/6i作为一线治疗。mPFS为28个月(R)对14个月(P)对6个月(A)(P = 0.002),一线治疗中接受R的患者比例更高。然而,当分析仅限于一线情况时,未发现差异(P = 0.193)。64例患者需要减少一剂,19例患者需要减少两剂。ORR为76.2%(R)对62%(P)对42.9%(A)。更多患者使用R和P实现了完全缓解,部分缓解和疾病稳定的发生率无差异。94.4%的人群发生了不良事件,最常见的3-4级不良事件是中性粒细胞减少(59.1%)。

结论

我们的结果证实了CDK4/6i在常规临床实践中的疗效和耐受性。这是描述和比较CDK4/6i在巴西人群中的疗效和毒性的首个真实世界数据。

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