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

被引:1
|
作者
Cannon, Timothy L. [1 ]
Rothe, Michael [2 ]
Mangat, Pam K. [2 ]
Garrett-Mayer, Elizabeth [2 ]
Chiu, Vi K. [3 ]
Hwang, Jimmy [4 ]
Vijayvergia, Namrata [5 ]
Alese, Olatunji B. [6 ]
Dib, Elie G. [7 ]
Duvivier, Herbert L. [8 ]
Klute, Kelsey A. [9 ]
Sahai, Vaibhav [10 ]
Ahn, Eugene R. [11 ]
Bedano, Pablo [12 ]
Behl, Deepti [13 ]
Sinclair, Sarah [14 ]
Thota, Ramya [15 ]
Urba, Walter J. [16 ]
Yang, Eddy S. [17 ]
Grantham, Gina N. [2 ]
Hinshaw, Dominique C. [2 ]
Gregory, Abigail [2 ]
Halabi, Susan [18 ]
Schilsky, Richard L. [2 ]
机构
[1] Inova Schar Canc Inst, Fairfax, VA USA
[2] Amer Soc Clin Oncol, Alexandria, VA 22314 USA
[3] Angeles Clin & Res Inst, Los Angeles, CA USA
[4] Atrium Hlth, Levine Canc Inst, Charlotte, NC USA
[5] Fox Chase Canc Ctr, Philadelphia, PA USA
[6] Emory Univ Winship Canc Inst, Atlanta, GA USA
[7] Michigan Canc Res Consortium, Ypsilanti, MI USA
[8] City Hope Atlanta, Newnan, GA USA
[9] Univ Nebraska, Med Ctr, Omaha, NE USA
[10] Univ Michigan, Rogel Canc Ctr, Ann Arbor, MI USA
[11] City Hope Chicago, Zion, IL USA
[12] Community Reg Canc Ctr, Indianapolis, IN USA
[13] Sutter Sacramento Med Ctr, Sacramento, CA USA
[14] Lafayette Family Canc Inst, Northern Light Canc Ctr, Brewer, ME USA
[15] Intermt Healthcare, Murray, UT USA
[16] Providence Canc Inst, Portland, OR USA
[17] Univ Kentucky, Coll Med, Markey Canc Ctr, Dept Radiat Med, Lexington, KY USA
[18] Duke Univ, Med Ctr, Durham, NC USA
关键词
OPEN-LABEL; CHOLANGIOCARCINOMA; CHEMOTHERAPY; MULTICENTER; TUMORS;
D O I
10.1200/JCO.23.02078
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. RESULTST wenty-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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页数:14
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