Literature DB >> 31126960

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 Le1, Vincent J Picozzi2, Andrew H Ko3, Zev A Wainberg4, Hedy Kindler5, Andrea Wang-Gillam6, Paul Oberstein7, Michael A Morse8, Herbert J Zeh9, Colin Weekes10, Tony Reid11, Erkut Borazanci12, Todd Crocenzi13, Noelle K LoConte14, Benjamin Musher15, Dan Laheru16, Aimee Murphy17, Chan Whiting17, Nitya Nair17, Amanda Enstrom17, Sandy Ferber18, Dirk G Brockstedt17, Elizabeth M Jaffee16.   

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. ©2019 American Association for Cancer Research.

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Year:  2019        PMID: 31126960     DOI: 10.1158/1078-0432.CCR-18-2992

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  63 in total

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Authors:  Andres Garcia-Sampedro; Gabriella Gaggia; Alexander Ney; Ismahan Mahamed; Pilar Acedo
Journal:  J Clin Med       Date:  2021-02-03       Impact factor: 4.241

Review 2.  Development of bacteria as diagnostics and therapeutics by genetic engineering.

Authors:  Daejin Lim; Miryoung Song
Journal:  J Microbiol       Date:  2019-05-11       Impact factor: 3.422

Review 3.  Current and emerging therapies for patients with advanced pancreatic ductal adenocarcinoma: a bright future.

Authors:  Eric S Christenson; Elizabeth Jaffee; Nilofer S Azad
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4.  Ipilimumab and Gemcitabine for Advanced Pancreatic Cancer: A Phase Ib Study.

Authors:  Suneel D Kamath; Aparna Kalyan; Sheetal Kircher; Halla Nimeiri; Angela J Fought; Al Benson; Mary Mulcahy
Journal:  Oncologist       Date:  2019-11-19

Review 5.  Landmark Series: Immunotherapy and Targeted Therapy for Pancreatic Cancer.

Authors:  Flavio G Rocha
Journal:  Ann Surg Oncol       Date:  2021-01-01       Impact factor: 5.344

Review 6.  Immunotherapy: Pancreatic Cancer and Extrahepatic Biliary Tract Cancer.

Authors:  Lukas Perkhofer; Alica K Beutel; Thomas J Ettrich
Journal:  Visc Med       Date:  2019-02-07

7.  Sterility of gamma-irradiated pathogens: a new mathematical formula to calculate sterilizing doses.

Authors:  Eve V Singleton; Shannon C David; Justin B Davies; Timothy R Hirst; James C Paton; Michael R Beard; Farhid Hemmatzadeh; Mohammed Alsharifi
Journal:  J Radiat Res       Date:  2020-11-16       Impact factor: 2.724

Review 8.  Dilemma and Challenge of Immunotherapy for Pancreatic Cancer.

Authors:  Jia Wu; Jianting Cai
Journal:  Dig Dis Sci       Date:  2020-03-05       Impact factor: 3.199

Review 9.  From state-of-the-art treatments to novel therapies for advanced-stage pancreatic cancer.

Authors:  Christopher Nevala-Plagemann; Manuel Hidalgo; Ignacio Garrido-Laguna
Journal:  Nat Rev Clin Oncol       Date:  2019-11-08       Impact factor: 66.675

Review 10.  New Treatment Strategies for Metastatic Pancreatic Ductal Adenocarcinoma.

Authors:  Ritu Raj Singh; Eileen M O'Reilly
Journal:  Drugs       Date:  2020-05       Impact factor: 9.546

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