drugset / Trial / NCT01730222

A Phase I-II Study of PAXG in Stage III-IV Pancreatic Adenocarcinoma

NCT01730222 ↗

Phase 1/2 Completed 137 enrolled IRCCS San Raffaele
RandomizedParallel-groupOpen-labelTreatment

Summary

Four-drug combo yielded a statistically significant improvement in progression-free survival and overall survival compared to gemcitabine in patients with advanced pancreatic adenocarcinoma. Nab-Paclitaxel showed promising antitumor activity in patients with pancreatic cancer. Given the synergism of taxanes with gemcitabine, fluoropyrimidines and platinating agents the role of nab-Paclitaxel in a 4-drug regimen will be explored. The aim of this trial is to determine the recommended dose of nab-paclitaxel in combination with cisplatin, capecitabine, and gemcitabine, PAXG regimen (Phase I), and to evaluate the feasibility and the activity of the PAXG regimen in patients with stage III and IV pancreatic cancer.

Timeline

Start
2012-11
Primary completion
2017-02
Completion
2017-08

Outcome

Met primary endpoint

paper Eight patients (31%) in the PAXG arm and nine (32%) in the AG arm underwent resection. PMID 30149366 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 1250 mg/m2 Oral
Subject Cisplatin Other / unclassified 30 mg/m2 —
Subject Gemcitabine Small molecule 800 mg/m2 —
Subject Gemcitabine Small molecule 1000 mg/m2 —
Subject Nab-paclitaxel Small molecule 125 mg/m2 —
Subject Nab-paclitaxel Small molecule 150 mg/m2 —