ERBB2/3基因改变的胆道癌患者使用帕妥珠单抗加曲妥珠单抗治疗:靶向药物和剖析利用登记研究的结果。

IF 42.1 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2024-05-15 DOI:10.1200/JCO.23.02078
Timothy L Cannon, Michael Rothe, Pam K Mangat, Elizabeth Garrett-Mayer, Vi K Chiu, Jimmy Hwang, Namrata Vijayvergia, Olatunji B Alese, Elie G Dib, Herbert L Duvivier, Kelsey A Klute, Vaibhav Sahai, Eugene R Ahn, Pablo Bedano, Deepti Behl, Sarah Sinclair, Ramya Thota, Walter J Urba, Eddy S Yang, Gina N Grantham, Dominique C Hinshaw, Abigail Gregory, Susan Halabi, Richard L Schilsky
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引用次数: 0

摘要

目的:靶向药物和分析利用登记处是一项II期篮子试验,评估市售靶向药物对晚期癌症患者的抗肿瘤活性,以及已知为药物靶点的基因组改变。本研究报告了一组接受培妥珠单抗加曲妥珠单抗治疗的ERBB2/3扩增、过表达或突变的胆道癌(BTC)患者的结果:符合条件的患者均为晚期胆道癌、可测量疾病(RECIST v1.1)、东部合作肿瘤学组(Eastern Cooperative Oncology Group)表现为0-2级、器官功能正常、肿瘤有ERBB2/3改变且缺乏标准治疗方案。该研究采用西蒙两阶段设计,主要终点为疾病控制(DC),根据RECIST v1.1标准定义为客观反应(OR)或至少持续16周以上的疾病稳定(SD16+)。次要终点包括客观反应(OR)、无进展生存期、总生存期、反应持续时间、疾病稳定持续时间和安全性:29名患者于2017年2月至2022年1月期间入组,所有患者均为晚期BTC,且存在ERBB2/3改变。一名患者无法进行疗效评估。观察到1例完全应答、8例部分应答和2例SD16+,DC和OR率分别为40%(90% CI,27至100)和32%(95% CI,16至52)。15%的DC率的零假设被拒绝(P = .0015)。四名患者至少出现了一次3级不良事件(AE)或严重AE,至少可能与治疗有关:贫血、腹泻、输液相关反应和疲劳:结论:泊珠单抗联合曲妥珠单抗符合预设标准,可宣布对患有BTC和ERBB2/3扩增、过表达或突变的患者具有活性信号。
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Pertuzumab Plus Trastuzumab in Patients With Biliary Tract Cancer With ERBB2/3 Alterations: Results From the Targeted Agent and Profiling Utilization Registry Study.

Purpose: Targeted Agent and Profiling Utilization Registry is a phase II basket trial evaluating the antitumor activity of commercially available targeted agents in patients with advanced cancer and genomic alterations known to be drug targets. Results of a cohort of patients with biliary tract cancer (BTC) with ERBB2/3 amplification, overexpression, or mutation treated with pertuzumab plus trastuzumab are reported.

Methods: Eligible patients had advanced BTC, measurable disease (RECIST v1.1), Eastern Cooperative Oncology Group performance status 0-2, adequate organ function, tumors with ERBB2/3 alterations, and a lack of standard treatment options. Simon's two-stage design was used with a primary end point of disease control (DC), defined as objective response (OR) or stable disease of at least 16+ weeks duration (SD16+) according to RECIST v1.1. Secondary end points included OR, progression-free survival, overall survival, duration of response, duration of stable disease, and safety.

Results: Twenty-nine patients were enrolled from February 2017 to January 2022, and all had advanced BTC with an ERBB2/3 alteration. One patient was not evaluable for efficacy. One complete response, eight partial responses, and two SD16+ were observed for DC and OR rates of 40% (90% CI, 27 to 100) and 32% (95% CI, 16 to 52), respectively. The null hypothesis of 15% DC rate was rejected (P = .0015). Four patients had at least one grade 3 adverse event (AE) or serious AE at least possibly related to treatment: anemia, diarrhea, infusion-related reaction, and fatigue.

Conclusion: Pertuzumab plus trastuzumab met prespecified criteria to declare a signal of activity in patients with BTC and ERBB2/3 amplification, overexpression, or mutation.

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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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