Results from a Phase IIb, Randomized, Multicenter Study of GVAX Pancreas and CRS-207 Compared with Chemotherapy in Adults with Previously Treated Metastatic Pancreatic Adenocarcinoma (ECLIPSE Study)

Dung T. Le(Sidney Kimmel Comprehensive Cancer Center), Vincent J. Picozzi(Virginia Mason Medical Center), Andrew H. Ko(University of California, San Francisco), Zev A. Wainberg(University of California, Los Angeles), Hedy L. Kindler(University of Chicago Medical Center), Andrea Wang‐Gillam(Washington University in St. Louis), Paul E. Oberstein(Columbia University Irving Medical Center), Michael A. Morse(Duke Medical Center), Herbert J. Zeh(University of Pittsburgh Medical Center), Colin D. Weekes(University of Colorado Cancer Center), Tony Reid(University of California San Diego), Erkut Borazanci(HonorHealth), Todd S. Crocenzi(Providence Portland Medical Center), Noelle K. LoConte(University of Wisconsin Carbone Cancer Center), Benjamin Musher(Baylor College of Medicine), Dan Laheru(Sidney Kimmel Comprehensive Cancer Center), Aimee Murphy(Aduro BioTech (United States)), Chan C. Whiting(Aduro BioTech (United States)), Nitya Nair(Aduro BioTech (United States)), Amanda Enstrom(Aduro BioTech (United States)), Sandy Ferber(University of Illinois Chicago), Dirk G. Brockstedt(Aduro BioTech (United States)), Elizabeth M. Jaffee(Sidney Kimmel Comprehensive Cancer Center)
Clinical Cancer Research
May 24, 2019
Cited by 260Open Access
Full Text

Abstract

Abstract Purpose: Limited options exist for patients with advanced pancreatic cancer progressing after 1 or more lines of therapy. A phase II study in patients with previously treated metastatic pancreatic cancer showed that combining GVAX pancreas (granulocyte-macrophage colony-stimulating factor-secreting allogeneic pancreatic tumor cells) with cyclophosphamide (Cy) and CRS-207 (live, attenuated Listeria monocytogenes expressing mesothelin) resulted in median overall survival (OS) of 6.1 months, which compares favorably with historical OS achieved with chemotherapy. In the current study, we compared Cy/GVAX + CRS-207, CRS-207 alone, and standard chemotherapy in a three-arm, randomized, controlled phase IIb trial. Patients and Methods: Patients with previously treated metastatic pancreatic adenocarcinoma were randomized 1:1:1 to receive Cy/GVAX + CRS-207 (arm A), CRS-207 (arm B), or physician's choice of single-agent chemotherapy (arm C). The primary cohort included patients who had failed ≥2 prior lines of therapy, including gemcitabine. The primary objective compared OS between arms A and C in the primary cohort. The second-line cohort included patients who had received 1 prior line of therapy. Additional objectives included OS between all treatment arms, safety, and tumor responses. Results: The study did not meet its primary efficacy endpoint. At the final study analysis, median OS [95% confidence interval (CI)] in the primary cohort (N = 213) was 3.7 (2.9–5.3), 5.4 (4.2–6.4), and 4.6 (4.2–5.7) months in arms A, B, and C, respectively, showing no significant difference between arm A and arm C [P = not significant (NS), HR = 1.17; 95% CI, 0.84–1.64]. The most frequently reported adverse events in all treatment groups were chills, pyrexia, fatigue, and nausea. No treatment-related deaths occurred. Conclusions: The combination of Cy/GVAX + CRS-207 did not improve survival over chemotherapy. (ClinicalTrials.gov ID: NCT02004262) See related commentary by Salas-Benito et al., p. 5435


Related Papers

No related papers found

Powered by citation graph analysis