Pembrolizumab in Patients With Tumors With High Tumor Mutational Burden: Results From the Targeted Agent and Profiling Utilization Registry Study

Herbert L. Duvivier(City Of Hope National Medical Center), Michael Rothe(American Society of Clinical Oncology), Pam K. Mangat(American Society of Clinical Oncology), Elizabeth Garrett‐Mayer(American Society of Clinical Oncology), Eugene R. Ahn(Cancer Treatment Centers of America), Tareq Al Baghdadi(Michigan Cancer Research Consortium), Ajjai Alva(University of Michigan), Stephanie A. Dublis(University of Michigan), Timothy Lewis Cannon(Virginia Cancer Institute), Carmen Calfa(University of Miami), Rui Li(Providence Portland Medical Center), Deepti Behl(Sutter Medical Center), Vi K. Chiu(Angeles Clinic and Research Institute), Philip J. Gold, Alissa Marr(University of Nebraska Medical Center), Kathryn F. Mileham(Levine Cancer Institute), Steven Powell(Sanford Health), Jordi Rodón(The University of Texas MD Anderson Cancer Center), Ramya Thota(Intermountain Healthcare), Gina N. Grantham(American Society of Clinical Oncology), Abigail Gregory(American Society of Clinical Oncology), Dominique C. Hinshaw(American Society of Clinical Oncology), Susan Halabi(Duke Medical Center), Richard L. Schilsky(American Society of Clinical Oncology)
Journal of Clinical Oncology
August 10, 2023
Cited by 41

Abstract

PURPOSE: The Targeted Agent and Profiling Utilization Registry (TAPUR) Study is a pragmatic basket trial evaluating antitumor activity of approved targeted agents in patients with advanced cancers harboring potentially actionable genomic alterations. Data from cohorts of patients with high tumor mutational burden (HTMB, defined as ≥9 mutations per megabase) with advanced colorectal cancer (CRC) and other advanced cancers treated with pembrolizumab are reported. METHODS: Eligible patients were 18 years and older with measurable tumors and a lack of standard treatment options, an Eastern Cooperative Oncology Group performance status of 0-1, and adequate organ function. The primary end point was disease control (DC), defined as complete or partial response or stable disease (SD) of at least 16-weeks duration. For the CRC cohort, Simon's two-stage design with a null DC rate of 15% versus 35% (power = 0.85; α = .10) was used. Low accruing histology-specific cohorts were collapsed into one histology-pooled (HP) cohort. For the HP cohort, the null hypothesis of a DC rate of 15% was rejected if the lower limit of a one-sided 90% CI was >15%. Secondary end points included objective response (OR), safety, progression-free survival, overall survival, duration of response, and duration of SD. RESULTS: = .04) and the OR rate was 11%. For the HP cohort, the DC rate was 45% (one-sided 90% CI, 35 to 100) and the OR rate was 26%. The null hypothesis of a 15% DC rate was rejected for both cohorts. Twelve of 77 patients experienced treatment-related grade 3 adverse events (AEs) or serious AEs, including two deaths. CONCLUSION: Pembrolizumab demonstrated antitumor activity in pretreated patients with advanced cancers and HTMB.


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