评估 CDK4/6 抑制剂在有症状和无症状转移性乳腺癌患者中的一线应用。

IF 3 4区 医学 Q2 ONCOLOGY
İrem Öner, Alper Türkel, Hicran Anık, Ülkü Yalçıntaş Arslan, Cengiz Karaçin
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引用次数: 0

摘要

研究背景本研究旨在比较CDK4/6抑制剂联合内分泌治疗对两类HR阳性/HER2阴性转移性乳腺癌患者的疗效:一类是有症状的高肿瘤负荷疾病患者,另一类是无症状疾病患者:这项回顾性研究纳入了193例接受ribociclib或palbociclib联合一线ET治疗的患者。患者被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:无症状患者的mPFS明显短于无症状患者(22.7个月对35.0个月,P = 0.009)。在无症状患者中,接受ribociclib治疗的患者的mPFS比接受palbociclib治疗的患者长(28.26个月 vs. 17.18个月,p = 0.021)。多变量分析发现,无症状疾病和肝转移是较短mPFS的独立预测因素(HR;1.835,95% CI;1.146-2.939和HR;2.433,95% CI;1.329-4.454):我们的分析表明,虽然与无症状患者相比,接受CDK4/6抑制剂加ET治疗的无症状患者的mPFS时间显著缩短,但22个月的mPFS表明CDK4/6抑制剂加ET是一种有效的治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of CDK4/6 inhibitors in first-line in symptomatic and asymptomatic patients with metastatic breast cancer.

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, p = 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, p = 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.

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来源期刊
Future oncology
Future oncology ONCOLOGY-
CiteScore
5.40
自引率
3.00%
发文量
335
审稿时长
4-8 weeks
期刊介绍: Future Oncology (ISSN 1479-6694) provides a forum for a new era of cancer care. The journal focuses on the most important advances and highlights their relevance in the clinical setting. Furthermore, Future Oncology delivers essential information in concise, at-a-glance article formats - vital in delivering information to an increasingly time-constrained community. The journal takes a forward-looking stance toward the scientific and clinical issues, together with the economic and policy issues that confront us in this new era of cancer care. The journal includes literature awareness such as the latest developments in radiotherapy and immunotherapy, concise commentary and analysis, and full review articles all of which provide key findings, translational to the clinical setting.
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