The CCTG PA.7 phase II trial of gemcitabine and nab-paclitaxel with or without durvalumab and tremelimumab as initial therapy in metastatic pancreatic ductal adenocarcinoma

Author:

Renouf Daniel J.ORCID,Loree Jonathan M.ORCID,Knox Jennifer J.,Topham James T.,Kavan Petr,Jonker Derek,Welch Stephen,Couture Felix,Lemay Frederic,Tehfe Mustapha,Harb Mohammed,Aucoin Nathalie,Ko Yoo-Joung,Tang Patricia A.,Ramjeesingh RaviORCID,Meyers Brandon M.,Kim Christina A.ORCID,Du Pan,Jia Shidong,Schaeffer David F.,Gill SharleneORCID,Tu Dongsheng,O’Callaghan Chris J

Abstract

AbstractImmunotherapy-based monotherapy treatment in metastatic pancreatic ductal adenocarcinoma (mPDAC) has shown limited benefit outside of the mismatch repair deficiency setting, while safety and efficacy of combining dual-checkpoint inhibitor immunotherapy with chemotherapy remains uncertain. Here, we present results from the CCTG PA.7 study (NCT02879318), a randomized phase II trial comparing gemcitabine and nab-paclitaxel with and without immune checkpoint inhibitors durvalumab and tremelimumab in 180 patients with mPDAC. The primary endpoint was overall survival. Secondary endpoints included progression-free survival and objective response rate. Results of the trial were negative as combination immunotherapy did not improve survival among the unselected patient population (p = 0.72) and toxicity was limited to elevation of lymphocytes in the combination immunotherapy group (p = 0.02). Exploratory baseline circulating tumor DNA (ctDNA) sequencing revealed increased survival for patients with KRAS wildtype tumors in both the combination immunotherapy (p = 0.001) and chemotherapy (p = 0.004) groups. These data support the utility of ctDNA analysis in PDAC and the prognostic value of ctDNA-based KRAS mutation status.

Funder

Terry Fox Research Institute

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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