Pertuzumab Plus Trastuzumab in Patients With Endometrial Cancer With ERBB2/3 Amplification, Overexpression, or Mutation: Results From the TAPUR Study

被引:21
作者
Ahn, Eugene R. [1 ]
Rothe, Michael [2 ]
Mangat, Pam K. [2 ]
Garrett-Mayer, Elizabeth [2 ]
Ali-Ahmad, Hussein M. [3 ]
Chan, John [4 ]
Maitland, Michael L. [5 ,6 ]
Patel, Sapna R. [7 ]
Reese, Zachary [8 ]
Balmanoukian, Ani S. [9 ]
Drescher, Charles W. [10 ]
Li, Rui [11 ]
Tsimberidou, Apostolia M. [12 ]
Leath, Charles A., III [13 ]
O'Lone, Raegan [2 ]
Grantham, Gina N. [2 ]
Halabi, Susan [14 ]
Schilsky, Richard L. [2 ]
机构
[1] City Hope Natl Med Ctr, Canc Treatment Ctr Amer Chicago, Zion, IL USA
[2] Amer Soc Clin Oncol, Alexandria, VA USA
[3] Michigan Canc Res Consortium, Lansing, MI USA
[4] Sutter Canc Res Consortium, San Francisco, CA USA
[5] Inova Schar Canc Inst, Fairfax, VA USA
[6] Univ Virginia, Comprehens Canc Ctr, Charlottesville, VA USA
[7] Canc Res Consortium West Michigan, St Joseph, MI USA
[8] Intermt Healthcare, Murray, UT USA
[9] Cedars Sinai Affiliate, Angeles Clin & Res Inst, Los Angeles, CA USA
[10] Swedish Canc Inst, Seattle, WA USA
[11] Providence Portland Med Ctr, Providence Canc Inst, Portland, OR USA
[12] Univ Texas MD Anderson Canc Ctr, Houston, TX USA
[13] Univ Alabama Birmingham, Sch Med, ONeal Comprehens Canc Ctr, Birmingham, AL USA
[14] Duke Univ, Med Ctr, Durham, NC USA
关键词
MOLECULAR PROFILES; SOLID TUMORS; HER2; RECEPTOR; EXPRESSION; P95HER2; GROWTH;
D O I
10.1200/PO.22.00609
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE The TAPUR Study is a pragmatic basket trial evaluating antitumor activity of commercially available targeted agents in patients with advanced cancers harboring potentially actionable genomic alterations. Data from a cohort of patients with endometrial cancer (EC) with ERBB2 or ERBB3 (ERBB2/3) amplification, overexpression, or mutation treated with pertuzumab plus trastuzumab (P + T) are reported.METHODSE ligible patients had advanced EC, no standard treatment options, measurable disease (RECIST v1.1), Eastern Cooperative Oncology Group performance status 0-2, adequate organ function, and tumors with ERBB2/3 amplification, overexpression, or mutation. Simon's two-stage design was used with a primary end point of disease control (DC), defined as objective response (OR) or stable disease (SD) of at least 16 weeks (SD16+) duration. Secondary end points include safety, duration of response, duration of SD, progression-free survival (PFS), and overall survival (OS).RESULTS Twenty-eight patients were enrolled from March 2017 to November 2019; all patients were evaluable for efficacy and toxicity. Seventeen patients had tumors with ERBB2/3 amplification and/or overexpression, eight with both ERBB2 amplification and ERBB2/3 mutations, and three with only ERBB2 mutations. Ten patients had DC (two partial response and eight SD16+); all 10 had ERBB2 amplification, and 6 of the 10 patients with DC had >1 ERBB2/3 alteration. DC and OR rates were 37% (95% CI, 21 to 50) and 7% (95% CI, 1 to 24), respectively; the median PFS and median OS were 16 weeks (95% CI, 10-28) and 61 weeks (95% CI, 24-105), respectively. One patient experienced a grade 3 serious adverse event (muscle weakness) at least possibly related to P + T.CONCLUSION P + T has antitumor activity in heavily pretreated patients with EC with ERBB2 amplification and warrants additional study.
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页数:12
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