Olaparib in Patients With Pancreatic Cancer With BRCA1/2 Mutations: Results From the Targeted Agent and Profiling Utilization Registry Study

Author:

Ahn Eugene R.1,Rothe Michael2,Mangat Pam K.2ORCID,Garrett-Mayer Elizabeth2ORCID,Calfa Carmen J.3ORCID,Alva Ajjai S.4,Suhag Vijay5,Alese Olatunji B.6ORCID,Dotan Efrat7ORCID,Hamid Omid8ORCID,Yang Eddy S.9ORCID,Marr Alissa S.10ORCID,Palmer Martin C.11,Thompson Forrest L.12,Yost Kathleen J.13,Gregory Abigail2ORCID,Grantham Gina N.2ORCID,Hinshaw Dominique C.2ORCID,Halabi Susan14ORCID,Schilsky Richard L.2ORCID

Affiliation:

1. City of Hope Chicago, Zion, IL

2. American Society of Clinical Oncology, Alexandria, VA

3. Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL

4. University of Michigan Rogel Comprehensive Cancer Center, Ann Arbor, MI

5. Sutter Health Roseville Cancer Center, Roseville, CA

6. Winship Cancer Institute of Emory University, Atlanta, GA

7. Fox Chase Cancer Center, Philadelphia, PA

8. The Angeles Clinic and Research Institute, A Cedars-Sinai Affiliate, Los Angeles, CA

9. Department of Radiation Oncology, O'Neal Comprehensive Cancer Center at the University of Alabama at Birmingham School of Medicine, Birmingham, AL

10. University of Nebraska Medical Center, Omaha, NE

11. Swedish Cancer Institute, Seattle, WA

12. Levine Cancer Institute, Atrium Health, Charlotte, NC

13. Cancer Research Consortium of West Michigan, Grand Rapids, MI

14. Duke University Medical Center, Durham, NC

Abstract

PURPOSE Targeted Agent and Profiling Utilization Registry (TAPUR) 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 advanced pancreatic cancer with BRCA1/ 2 mutations treated with olaparib are reported. METHODS Eligible patients had advanced pancreatic cancer, measurable disease, Eastern Cooperative Oncology Group performance status 0-2, adequate organ function, and no standard treatment options available. Genomic testing was performed in Clinical Laboratory Improvement Amendments–certified, College of American Pathologists-accredited site selected laboratories. 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 (PFS), overall survival (OS), duration of response, duration of stable disease, and safety. RESULTS Thirty patients with BRCA1/ 2 mutations were enrolled from November 2016 to August 2019. The median number of reported previous therapies was 3 (range, 1-10). Two patients were not evaluable and excluded from efficacy analyses. Two patients with complete response, three with partial response and three with SD16+, were observed for DC and OR rates of 31% (90% CI, 18 to 40; P = .04) and 18% (95% CI, 6 to 37), respectively. The median PFS was 8 (95% CI, 8 to 15) weeks, and the median OS was 38 (95% CI, 21 to 65) weeks. Three patients had at least one drug-related grade 3 adverse event or serious adverse event of anemia, fever, or oral mucositis. CONCLUSION Olaparib showed antitumor activity in patients with advanced pancreatic cancer with BRCA1/ 2 mutations extending findings of recent studies of olaparib in patients with this disease.

Publisher

American Society of Clinical Oncology (ASCO)

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