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Modified FOLFIRINOX for resected pancreatic cancer: Opportunities and challenges
- Source :
- World Journal of Gastroenterology
- Publication Year :
- 2019
- Publisher :
- Baishideng Publishing Group Inc, 2019.
-
Abstract
- Pancreatic cancer is one of the leading causes of cancer death worldwide. Adjuvant chemotherapy has been developed based on the experiences made with palliative chemotherapy, and advocated to improve long-term survival of patients with this disease. However, the optimal chemotherapeutic regimen remains controversial. Recently, Conroy et al demonstrated the impressive benefits of modified FOLFIRINOX over gemcitabine alone in the multicenter Partenariat de Recherche en Oncologie Digestive 24 (PRODIGE-24) trial. The remarkable results mark a new milestone in treating resectable pancreatic cancer and have now changed the standard of care for this patient population. In this commentary, we discuss an issue of difference of tumor grade between the PRODIGE-24 trial and previous phase III trials. We also discuss potential biomarkers predicting therapeutic response to modified FOLFIRINOX. Finally, we summarize several ongoing clinical trials of replacing part of the FOLFIRINOX regimen with Xeloda/S-1/nanoliposomal irinotecan for pancreatic cancer.
- Subjects :
- Oncology
medicine.medical_specialty
FOLFIRINOX
Leucovorin
Field Of Vision
Irinotecan
Deoxycytidine
Adjuvant therapy
03 medical and health sciences
0302 clinical medicine
Pancreatic cancer
Internal medicine
Germany
Neutrophil-to-lymphocyte
Antineoplastic Combined Chemotherapy Protocols
medicine
Humans
business.industry
Gastroenterology
General Medicine
medicine.disease
Nanoliposomal irinotecan
Gemcitabine
Clinical trial
Pancreatic Neoplasms
Regimen
030220 oncology & carcinogenesis
030211 gastroenterology & hepatology
Folfirinox Regimen
Fluorouracil
business
medicine.drug
Subjects
Details
- Language :
- English
- ISSN :
- 22192840 and 10079327
- Volume :
- 25
- Issue :
- 23
- Database :
- OpenAIRE
- Journal :
- World Journal of Gastroenterology
- Accession number :
- edsair.doi.dedup.....c5e5e894d61ef3704ed3ae32bc4481e6