Pertuzumab Plus Trastuzumab in Patients With Biliary Tract Cancer With <i>ERBB2/3</i> Alterations: Results From the Targeted Agent and Profiling Utilization Registry Study

Timothy Lewis Cannon(Virginia Cancer Institute), Michael Rothe(American Society of Clinical Oncology), Pam K. Mangat(American Society of Clinical Oncology), Elizabeth Garrett‐Mayer(American Society of Clinical Oncology), Vi K. Chiu(Angeles Clinic and Research Institute), Jimmy J. Hwang(Levine Cancer Institute), Namrata Vijayvergia(Fox Chase Cancer Center), Olatunji B. Alese(Emory University), Elie G. Dib(Michigan Cancer Research Consortium), Herbert L. Duvivier(City of Hope), Kelsey Klute(University of Nebraska Medical Center), Vaibhav Sahai(University of Michigan), Eugene R. Ahn(City of Hope), Pablo M. Bedano(Community Cancer Center), Deepti Behl(Sutter Medical Center), Sarah Sinclair, Ramya Thota(Intermountain Healthcare), Walter J. Urba(Providence Portland Medical Center), Eddy S. Yang(University of Kentucky), Gina N. Grantham(American Society of Clinical Oncology), Dominique C. Hinshaw(American Society of Clinical Oncology), Abigail Gregory(American Society of Clinical Oncology), Susan Halabi(Duke Medical Center), Richard L. Schilsky(American Society of Clinical Oncology)
Journal of Clinical Oncology
May 15, 2024
Cited by 22

Abstract

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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