drugset / Trial / NCT04793932

Short-course Versus Long-course Pre-operative Chemotherapy With mFOLFIRINOX or PAXG (CASSANDRA TRIAL)

NCT04793932 ↗

RandomizedFactorialOpen-labelTreatment

Summary

The main aim of this study is to compare the efficacy of short-course versus long-course pre-operative chemotherapy with PAXG or mFOLFIRINOX in patients who receive a diagnosis of pancreatic ductal adenocarcinoma (PDAC) resectable or borderline resectable.

Timeline

Start
2020-11-03
Primary completion
2025-03-15
Completion
2026-01-31

Outcome

Met primary endpoint

paper PAXG prolonged the median EFS compared with mFOLFIRINOX (16·0 months [95% CI 12·4-19·8] vs 10·2 months [8·6-13·5]; hazard ratio 0·63 [0·47-0·84]; p=0·0018). PMID 41275879 ↗

paper PAXG significantly improved EFS compared with mFOLFIRINOX in resectable or borderline resectable PDAC. PMID 41275879 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 1250 mg/m2 Oral
Subject Cisplatin Other / unclassified 30 mg/m2 Intravenous
Subject Gemcitabine Small molecule 800 mg/m2 Intravenous
Subject Irinotecan Small molecule 150 mg/m2 —
Subject Leucovorin Small molecule 400 mg/m2 —
Subject Nab-paclitaxel Small molecule 150 mg/m2 Intravenous
Subject Oxaliplatin Small molecule 85 mg/m2 —
Subject fluorouracil Small molecule 2400 mg/m2 Intravenous