Regine William F, Winter Kathryn A, Abrams Ross A, Safran Howard, Hoffman John P, Konski Andre, Benson Al B, Macdonald John S, Kudrimoti Mahesh R, Fromm Mitchel L, Haddock Michael G, Schaefer Paul, Willett Christopher G, Rich Tyvin A
Department of Radiation Oncology, University of Maryland Medical Center, Baltimore 21030, USA.
JAMA. 2008 Mar 5;299(9):1019-26. doi: 10.1001/jama.299.9.1019.
Among patients with locally advanced metastatic pancreatic adenocarcinoma, gemcitabine has been shown to improve outcomes compared with fluorouracil.
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.
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).
Survival for all patients and survival for patients with pancreatic head tumors were the primary end points. Secondary end points included toxicity.
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%).
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.
clinicaltrials.gov Identifier: NCT00003216.
在局部晚期转移性胰腺腺癌患者中,与氟尿嘧啶相比,吉西他滨已显示可改善治疗效果。
确定在辅助性氟尿嘧啶放化疗(化疗加放疗)中添加吉西他滨是否能提高切除的胰腺腺癌患者的生存率。
设计、地点和参与者:1998年7月至2002年7月期间招募的胰腺腺癌完全根治性切除且未接受过放疗或化疗的患者的随机对照3期试验,在美国和加拿大的164家机构进行随访,直至2006年8月18日。
在放化疗前3周及放化疗后12周,采用氟尿嘧啶(每天持续输注250mg/m²;n = 230)或吉西他滨(每周一次30分钟输注1000mg/m²;n = 221)进行化疗。所有患者的放化疗均采用持续输注氟尿嘧啶(每天250mg/m²)(50.4Gy)。
所有患者的生存率和胰头肿瘤患者的生存率为主要终点。次要终点包括毒性。
共有451例患者被随机分组、符合条件并可进行分析。胰头肿瘤患者(n = 388)中,吉西他滨组的中位生存期为20.5个月,3年生存率为31%;氟尿嘧啶组的中位生存期为16.9个月,3年生存率为22%(风险比,0.82[95%置信区间,0.65 - 1.03];P = 0.09)。多因素分析增强了治疗效果(风险比,0.80[95%置信区间,0.63 - 1.00];P = 0.05)。4级血液学毒性在氟尿嘧啶组为1%,在吉西他滨组为14%(P < 0.001),发热性中性粒细胞减少或感染无差异。完成化疗或放疗的能力无差异(>85%)。
辅助性氟尿嘧啶放化疗中添加吉西他滨对切除的胰腺癌患者有生存获益,尽管这种改善无统计学意义。
clinicaltrials.gov标识符:NCT00003216。