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接受以哌柏西利为基础的联合治疗的转移性内分泌反应性乳腺癌患者的真实世界转归

Real-world outcomes of patients with metastatic endocrine-responsive breast cancer receiving palbociclib-based combinations.

作者信息

Moser Sarah Sharman, Mazursky Orr Friedman, Shalev Hadas, Apter Lior, Chodick Gabriel, Siegelmann-Danieli Nava

机构信息

Maccabi Institute for Research & Innovation, Maccabi Healthcare Services, Kaufman 4, Tel Aviv, 6801296, Israel.

Medical Affairs, Pfizer Pharmaceuticals Israel, Shenker 9, Herzlia, 4672509 Israel.

出版信息

Future Oncol. 2023 Jul;19(21):1473-1483. doi: 10.2217/fon-2023-0176. Epub 2023 Aug 2.

Abstract

To describe treatment journey and clinical outcomes after palbociclib initiation in HR+/HER2- breast cancer patients across multiple lines. Adult patients (n = 559) were identified in a population-based study between January 2018 and June 2020. Median follow-up time was 41.2 months. The starting dose was 125 mg for more than 85% of patients, and a third had dose reduction. Median time on treatment was 30.5 months for palbociclib + aromatase inhibitors for patients that received first-line treatment after metastatic diagnosis, and 12.6 months for palbociclib + fulvestrant across multiple lines, and longer for patients that had a dose reduction during treatment. At 48 months, 59.3 and 27.3% of patients were still alive, respectively. Subsequent lines resulted in median time on treatment of 4.4-7.7 months in both groups. Time on treatment for palbociclib was comparable to data from clinical trials, and follow-up allowed us to examine subsequent treatment after initial treatment failure. Dose reduction was common in the real-world setting and did not adversely affect efficacy.

摘要

描述多线治疗的HR+/HER2-乳腺癌患者开始使用哌柏西利后的治疗过程和临床结果。在一项基于人群的研究中,于2018年1月至2020年6月期间确定了成年患者(n = 559)。中位随访时间为41.2个月。超过85%的患者起始剂量为125mg,三分之一的患者进行了剂量降低。对于转移性诊断后接受一线治疗的患者,哌柏西利+芳香化酶抑制剂的中位治疗时间为30.5个月,多线使用哌柏西利+氟维司群的中位治疗时间为12.6个月,治疗期间进行剂量降低的患者治疗时间更长。在48个月时,患者的生存率分别为59.3%和27.3%。两组后续治疗的中位治疗时间均为4.4 - 7.7个月。哌柏西利的治疗时间与临床试验数据相当,随访使我们能够检查初始治疗失败后的后续治疗情况。在现实环境中,剂量降低很常见,且对疗效没有不利影响。

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