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Sorafenib does not improve efficacy of chemotherapy in advanced pancreatic cancer: A GISCAD randomized phase II study
- Publication Year :
- 2014
-
Abstract
- Background: The RAF-MEK-ERK pathway is commonly activated in pancreatic cancer because of a high frequency of KRAS-BRAF mutations. A phase II randomized trial was designed to investigate the activity of sorafenib in combination with chemotherapy in advanced pancreatic cancer. Methods: Locally advanced or metastatic pancreatic adenocarcinoma patients were randomized in a 1:1 ratio to receive cisplatin plus gemcitabine with sorafenib 400. mg bid (arm A) or without sorafenib (arm B). Results: One hundred and fourteen patients were enrolled; of these, 43 (74.6%) patients progressed in arm A and 44 (82.4%) in arm B. Median progression-free survival was 4.3 months (95% CI: 2.7-6.5) and 4.5 months (95% CI: 2.5-5.2), respectively (HR = 0.92; 95% CI: 0.62-1.35). Median overall survival was 7.5 (95% CI: 5.6-9.7) and 8.3 months (95% CI: 6.2-8.7), respectively (HR = 0.95; 95% CI: 0.62-1.48). Response rates were 3.4% in arm A and 3.6% in arm B. Conclusions: Sorafenib does not significantly enhance activity of chemotherapy in advanced pancreatic cancer patients, and therefore should not be assessed in phase III trials. © 2013 Editrice Gastroenterologica Italiana S.r.l.
- Subjects :
- Oncology
Sorafenib
Male
Niacinamide
medicine.medical_specialty
medicine.medical_treatment
Phase II study
pancreatic cancer
Phases of clinical research
Adenocarcinoma
Deoxycytidine
Disease-Free Survival
chemistry.chemical_compound
Internal medicine
Pancreatic cancer
Antineoplastic Combined Chemotherapy Protocols
medicine
80 and over
Humans
Aged
Aged, 80 and over
Chemotherapy
Hepatology
business.industry
Phenylurea Compounds
Gastroenterology
Metastatic Pancreatic Adenocarcinoma
Middle Aged
medicine.disease
Gemcitabine
Cisplatin
Female
Pancreatic Neoplasms
Treatment Outcome
chemistry
business
medicine.drug
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....f0c7e4be73da3a6b3b3b0d16034b0143