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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).
Le, Dung T; Picozzi, Vincent J; Ko, Andrew H; Wainberg, Zev A; Kindler, Hedy; Wang-Gillam, Andrea; Oberstein, Paul; Morse, Michael A; Zeh, Herbert J; Weekes, Colin; Reid, Tony; Borazanci, Erkut; Crocenzi, Todd; LoConte, Noelle K; Musher, Benjamin; Laheru, Dan; Murphy, Aimee; Whiting, Chan; Nair, Nitya; Enstrom, Amanda; Ferber, Sandy; Brockstedt, Dirk G; Jaffee, Elizabeth M.
Affiliation
  • Le DT; The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland. dle@jhmi.edu.
  • Picozzi VJ; Virginia Mason Medical Center, Seattle, Washington.
  • Ko AH; University of California San Francisco, San Francisco, California.
  • Wainberg ZA; University of California Los Angeles, Los Angeles, California.
  • Kindler H; University of Chicago Medical Center, Chicago, Illinois.
  • Wang-Gillam A; Washington University School of Medicine in St. Louis, St. Louis, Missouri.
  • Oberstein P; Columbia University Medical Center, New York, New York.
  • Morse MA; Duke University Medical Center, Durham, North Carolina.
  • Zeh HJ; University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
  • Weekes C; University of Colorado Cancer Center, Aurora, Colorado.
  • Reid T; University of San Diego Moores Cancer Center, La Jolla, California.
  • Borazanci E; HonorHealth, Tgen, Scottsdale, Arizona.
  • Crocenzi T; Providence Cancer Center, Portland, Oregon.
  • LoConte NK; University of Wisconsin Carbone Cancer Center, Madison, Wisconsin.
  • Musher B; Baylor College of Medicine, Houston, Texas.
  • Laheru D; The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland.
  • Murphy A; Aduro Biotech, Berkeley, California.
  • Whiting C; Aduro Biotech, Berkeley, California.
  • Nair N; Aduro Biotech, Berkeley, California.
  • Enstrom A; Aduro Biotech, Berkeley, California.
  • Ferber S; Array Biostatistics, LLC, Chicago, Illinois.
  • Brockstedt DG; Aduro Biotech, Berkeley, California.
  • Jaffee EM; The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland.
Clin Cancer Res ; 25(18): 5493-5502, 2019 Sep 15.
Article de En | MEDLINE | ID: mdl-31126960
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 111 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.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs du pancréas / Adénocarcinome Type d'étude: Clinical_trials Limites: Adult / Humans Langue: En Journal: Clin Cancer Res Sujet du journal: NEOPLASIAS Année: 2019 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs du pancréas / Adénocarcinome Type d'étude: Clinical_trials Limites: Adult / Humans Langue: En Journal: Clin Cancer Res Sujet du journal: NEOPLASIAS Année: 2019 Type de document: Article