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曲妥珠单抗用于HER2阳性转移性乳腺癌进展后治疗:一线治疗的无进展生存期可预测对总生存期的影响。

Trastuzumab beyond progression for HER2 positive metastatic breast cancer: progression-free survival on first-line therapy predicts overall survival impact.

作者信息

Rayson Daniel, Lutes Sarah, Walsh Gordon, Sellon Marlene, Colwell Bruce, Dorreen Mark, Drucker Arik, Jeyakumar Alwin, Younis Tallal

机构信息

Division of Medical Oncology, Queen Elizabeth II Health Sciences Centre and Atlantic Clinical Cancer Research Unit, Halifax, NS, Canada.

出版信息

Breast J. 2014 Jul-Aug;20(4):408-13. doi: 10.1111/tbj.12284.

Abstract

Trastuzumab beyond first progression in the metastatic setting has been adopted based on limited data suggesting improved outcomes compared to second-line chemotherapy alone although predictive factors for preferential benefit remain elusive. We conducted a retrospective review of all patients receiving trastuzumab for HER2 + metastatic disease between Jan 1, 1999-June 15, 2011. Univariate and time to event analyses described treatment and survival patterns. Median duration of each line of therapy and overall survival times for covariates, including treatment era (pre versus post Jan 1, 2005), lines of trastuzumab-based therapy (1 versus 2 versus 3 + ), first-line chemotherapy partner (docetaxel/paclitaxel versus other) and median exposure to first-line trastuzumab-based therapy (=/> versus < cohort median) were estimated. A total of 119 patients received a median of two lines of trastuzumab-based therapy (range 1-8). Median overall survival was 21.8 months (95% CI = 14.5-27.1 m), by era was 15.6 m (95% CI = 9.7-24.8 m) versus 26.1 m (95% CI = 20.0-39.3 m; p = 0.11) and by lines of trastuzumab-based therapy received was 10.6 m (95% CI = 5.3-17.4 m) versus 13.9 m (95% CI = 9.5-27.6 m) versus 32.5 m (95% CI = 25-49.4 m) (p = 0.0014). Median overall survival was significantly longer for those receiving taxanes with trastuzumab compared to other first line partners (26.1 m, 95% CI = 17.8-31.4 m versus 14.5 m, 95% CI = 9.4-21.9 m, p = 0.02). Median overall survival with duration of first-line trastuzumab-based therapy =/> cohort median was 31.9 m (95% CI = 26.2-52.2 m) versus 10.3 m for shorter durations (95% CI = 6.9-15.6 m; p < 0.0001). Our observations support progression-free survival on first-line trastuzumab-based therapy as a clinically relevant predictive factor for overall survival benefit with the adoption of a trastuzumab beyond progression treatment strategy.

摘要

尽管二线化疗单独使用时,曲妥珠单抗在转移性疾病一线进展后的应用所依据的数据有限,但提示其与单独二线化疗相比能改善预后,且优先获益的预测因素仍不明确。我们对1999年1月1日至2011年6月15日期间接受曲妥珠单抗治疗HER2+转移性疾病的所有患者进行了回顾性研究。单因素分析和事件发生时间分析描述了治疗和生存模式。估计了各线治疗的中位持续时间以及协变量的总生存时间,包括治疗时代(2005年1月1日之前与之后)、基于曲妥珠单抗的治疗线数(1线与2线与3线及以上)、一线化疗联合用药(多西他赛/紫杉醇与其他)以及一线基于曲妥珠单抗治疗的中位暴露时间(≥/>与<队列中位数)。共有119例患者接受了中位两线基于曲妥珠单抗的治疗(范围1 - 8线)。中位总生存时间为21.8个月(95%置信区间 = 14.5 - 27.1个月),按时代划分,2005年1月1日之前为15.6个月(95%置信区间 = 9.7 - 24.8个月),2005年1月1日之后为26.1个月(95%置信区间 = 20.0 - 39.3个月;p = 0.11),按接受的基于曲妥珠单抗的治疗线数划分,1线为10.6个月(95%置信区间 = 5.3 - 17.4个月),2线为13.9个月(95%置信区间 = 9.5 - 27.6个月),3线及以上为32.5个月(95%置信区间 = 25 - 49.4个月)(p = 0.0014)。与其他一线联合用药相比,接受曲妥珠单抗联合紫杉类药物治疗的患者中位总生存时间显著更长(26.1个月,95%置信区间 = 17.8 - 31.4个月,而其他为14.5个月,95%置信区间 = 9.4 - 21.9个月,p = 0.02)。一线基于曲妥珠单抗治疗持续时间≥/>队列中位数的患者中位总生存时间为31.9个月(95%置信区间 = 26.2 - 52.2个月),而持续时间较短者为10.3个月(95%置信区间 = 6.9 - 15.6个月;p < 0.0001)。我们的观察结果支持一线基于曲妥珠单抗治疗的无进展生存作为采用曲妥珠单抗进展后治疗策略获得总生存获益的临床相关预测因素。

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