Evaluation of Cyclophosphamide/GVAX Pancreas Followed by Listeria-Mesothelin (CRS-207) with or without Nivolumab in Patients with Pancreatic Cancer.
Cancer Vaccines
/ administration & dosage
Combined Modality Therapy
/ methods
Cyclophosphamide
/ administration & dosage
GPI-Linked Proteins
/ genetics
Immunotherapy
/ methods
Kaplan-Meier Estimate
Listeria monocytogenes
/ genetics
Mesothelin
Nivolumab
/ administration & dosage
Pancreas
/ drug effects
Pancreatic Neoplasms
/ immunology
Progression-Free Survival
Response Evaluation Criteria in Solid Tumors
Vaccines, Attenuated
/ administration & dosage
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500
Informations de publication
Date de publication:
15 07 2020
15 07 2020
Historique:
received:
22
12
2019
revised:
23
02
2020
accepted:
03
04
2020
pubmed:
11
4
2020
medline:
3
11
2021
entrez:
11
4
2020
Statut:
ppublish
Résumé
Two studies in previously treated metastatic pancreatic cancer have been completed combining GVAX pancreas vaccine (GM-CSF-secreting allogeneic pancreatic tumor cells) with cyclophosphamide (Cy) and CRS-207 (live, attenuated Patients with pancreatic adenocarcinoma who received one prior therapy for metastatic disease and RECIST measurable disease were randomized 1:1 to receive treatment on Arm A or Arm B. The primary objective was to compare overall survival (OS) between the arms. Additional objectives included assessment of progression-free survival, safety, tumor responses, CA19-9 responses, and immunologic correlates. Ninety-three patients were treated (Arm A, 51; Arm B, 42). The median OS in Arms A and B were 5.9 [95% confidence interval (CI), 4.7-8.6] and 6.1 (95% CI, 3.5-7.0) months, respectively, with an HR of 0.86 (95% CI, 0.55-1.34). Objective responses were seen in 3 patients using immune-related response criteria (4%, 2/51, Arm A; 2%, 1/42, Arm B). The grade ≥3 related adverse event rate, whereas higher in Arm A (35.3% vs. 11.9%) was manageable. Changes in the microenvironment, including increase in CD8 Although the study did not meet its primary endpoint of improvement in OS of Arm A over Arm B, the OS was comparable with standard therapy. Objective responses and immunologic changes in the tumor microenvironment were evident.
Identifiants
pubmed: 32273276
pii: 1078-0432.CCR-19-3978
doi: 10.1158/1078-0432.CCR-19-3978
pmc: PMC7727397
mid: NIHMS1606711
doi:
Substances chimiques
Cancer Vaccines
0
GPI-Linked Proteins
0
GVAX vaccine
0
Vaccines, Attenuated
0
Nivolumab
31YO63LBSN
Cyclophosphamide
8N3DW7272P
Mesothelin
J27WDC343N
Types de publication
Clinical Trial, Phase II
Comparative Study
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
3578-3588Subventions
Organisme : NCI NIH HHS
ID : U01 CA224012
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM136577
Pays : United States
Organisme : NCI NIH HHS
ID : R50 CA243627
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA197296
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA062924
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA006973
Pays : United States
Informations de copyright
©2020 American Association for Cancer Research.
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