Fluorouracil vs gemcitabine chemotherapy before and after fluorouracil-based chemoradiation following resection of pancreatic adenocarcinoma: a randomized controlled trial
- PMID: 18319412
- DOI: 10.1001/jama.299.9.1019
Fluorouracil vs gemcitabine chemotherapy before and after fluorouracil-based chemoradiation following resection of pancreatic adenocarcinoma: a randomized controlled trial
Erratum in
- JAMA. 2008 Apr 23/30;299(16):1902
Abstract
Context: Among patients with locally advanced metastatic pancreatic adenocarcinoma, gemcitabine has been shown to improve outcomes compared with fluorouracil.
Objective: To determine if the addition of gemcitabine to adjuvant fluorouracil chemoradiation (chemotherapy plus radiation) improves survival for patients with resected pancreatic adenocarcinoma.
Design, setting, and participants: Randomized controlled phase 3 trial of patients with complete gross total resection of pancreatic adenocarcinoma and no prior radiation or chemotherapy enrolled between July 1998 and July 2002 with follow-up through August 18, 2006, at 164 US and Canadian institutions.
Intervention: Chemotherapy with either fluorouracil (continuous infusion of 250 mg/m2 per day; n = 230) or gemcitabine (30-minute infusion of 1000 mg/m2 once per week; n = 221) for 3 weeks prior to chemoradiation therapy and for 12 weeks after chemoradiation therapy. Chemoradiation with a continuous infusion of fluorouracil (250 mg/m2 per day) was the same for all patients (50.4 Gy).
Main outcome measures: Survival for all patients and survival for patients with pancreatic head tumors were the primary end points. Secondary end points included toxicity.
Results: A total of 451 patients were randomized, eligible, and analyzable. Patients with pancreatic head tumors (n = 388) had a median survival of 20.5 months and a 3-year survival of 31% in the gemcitabine group vs a median survival of 16.9 months and a 3-year survival of 22% in the fluorouracil group (hazard ratio, 0.82 [95% confidence interval, 0.65-1.03]; P = .09). The treatment effect was strengthened on multivariate analysis (hazard ratio, 0.80 [95% confidence interval, 0.63-1.00]; P = .05). Grade 4 hematologic toxicity was 1% in the fluorouracil group and 14% in the gemcitabine group (P < .001) without a difference in febrile neutropenia or infection. There were no differences in the ability to complete chemotherapy or radiation therapy (>85%).
Conclusions: The addition of gemcitabine to adjuvant fluorouracil-based chemoradiation was associated with a survival benefit for patients with resected pancreatic cancer, although this improvement was not statistically significant.
Trial registration: clinicaltrials.gov Identifier: NCT00003216.
Comment in
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Adjuvant therapy for surgically resected pancreatic adenocarcinoma.JAMA. 2008 Mar 5;299(9):1066-7. doi: 10.1001/jama.299.9.1066. JAMA. 2008. PMID: 18319419 No abstract available.
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Survival for patients with pancreatic cancer after addition of gemcitabine to fluorouracil chemoradiation.JAMA. 2008 Jun 25;299(24):2852; author reply 2852-3. doi: 10.1001/jama.299.24.2852-b. JAMA. 2008. PMID: 18577724 No abstract available.
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Survival for patients with pancreatic cancer after addition of gemcitabine to Fluorouracil chemoradiation.JAMA. 2008 Jun 25;299(24):2852; author reply 2852-3. doi: 10.1001/jama.299.24.2852-a. JAMA. 2008. PMID: 18577725 No abstract available.
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