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CDK4/6抑制剂在有症状和无症状转移性乳腺癌一线治疗中的评估。

Evaluation of CDK4/6 inhibitors in first-line in symptomatic and asymptomatic patients with metastatic breast cancer.

作者信息

Öner İrem, Türkel Alper, Anık Hicran, Arslan Ülkü Yalçıntaş, Karaçin Cengiz

机构信息

Department of Medical Oncology, Dr. Abdurrahman Yurtaslan Ankara Oncology Research and Training Hospital Ankara, Ankara, Turkey.

出版信息

Future Oncol. 2024 Dec;20(40):3443-3450. doi: 10.1080/14796694.2024.2432850. Epub 2024 Nov 26.

DOI:10.1080/14796694.2024.2432850
PMID:39589751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11776864/
Abstract

BACKGROUND

This study aimed to compare the efficacy of CDK4/6 inhibitors plus endocrine therapy in two groups of patients with HR-positive/HER2-negative metastatic breast cancer: those with symptomatic, high tumor burden disease and those with asymptomatic disease.

DESIGN AND METHODS

This retrospective study included 193 patients who received either ribociclib or palbociclib in combination with first-line ET. Patients were divided into symptomatic and asymptomatic groups and compared regarding baseline characteristics and progression-free survivals (PFS).

RESULTS

Symptomatic patients had a significantly shorter mPFS than asymptomatic patients (22.7 months vs. 35.0 months,  = 0.009). Among symptomatic patients, those treated with ribociclib had a longer mPFS than those treated with palbociclib (28.26 months vs. 17.18 months,  = 0.021). Multivariate analysis identified the symptomatic disease and liver metastasis as independent predictors of shorter mPFS (HR; 1.835, 95% CI; 1.146-2.939 and HR; 2.433, 95% CI; 1.329-4.454, respectively).

CONCLUSION

Our analysis revealed that although symptomatic individuals who underwent CDK4/6 inhibitor plus ET experienced a significant reduction in mPFS durations compared to asymptomatic patients, the 22-month mPFS indicated that CDK4/6 inhibitor plus ET is an effective treatment option.

摘要

背景

本研究旨在比较CDK4/6抑制剂联合内分泌治疗在两组激素受体阳性/人表皮生长因子受体2阴性转移性乳腺癌患者中的疗效:有症状、高肿瘤负荷疾病患者和无症状疾病患者。

设计与方法

这项回顾性研究纳入了193例接受瑞博西尼或哌柏西利联合一线内分泌治疗的患者。患者分为有症状组和无症状组,并就基线特征和无进展生存期(PFS)进行比较。

结果

有症状患者的中位无进展生存期显著短于无症状患者(22.7个月对35.0个月,P = 0.009)。在有症状患者中,接受瑞博西尼治疗的患者中位无进展生存期长于接受哌柏西利治疗的患者(28.26个月对17.18个月,P = 0.021)。多因素分析确定有症状疾病和肝转移是中位无进展生存期较短的独立预测因素(风险比分别为1.835,95%置信区间为1.146 - 2.939;风险比为2.433,95%置信区间为1.329 - 4.454)。

结论

我们的分析表明,尽管与无症状患者相比,接受CDK4/6抑制剂联合内分泌治疗的有症状个体的中位无进展生存期显著缩短,但22个月的中位无进展生存期表明CDK4/6抑制剂联合内分泌治疗是一种有效的治疗选择。

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