首页> 外文期刊>British Journal of Cancer >A multicenter phase III trial comparing irinotecan-gemcitabine (IG) with gemcitabine (G) monotherapy as first-line treatment in patients with locally advanced or metastatic pancreatic cancer
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A multicenter phase III trial comparing irinotecan-gemcitabine (IG) with gemcitabine (G) monotherapy as first-line treatment in patients with locally advanced or metastatic pancreatic cancer

机译:一项多中心III期试验,比较了伊立替康-吉西他滨(IG)与吉西他滨(G)单药治疗作为局部晚期或转移性胰腺癌患者的一线治疗

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Our purpose was to determine the response rate and median and overall survival of gemcitabine as monotherapy versus gemcitabine plus irinotecan in advanced or metastatic pancreatic cancer. Patients with histologically or cytologically confirmed adenocarcinoma who were chemotherapy and radiotherapy naive were enrolled. Patients were centrally randomised at a one-to-one ratio to receive either gemcitabine monotherapy (900?mg?m?2 on days 1, 8 and 15 every 4 weeks (arm G), or gemcitabine (days 1 and 8) plus irinotecan (300?mg?m?2 on day 8) (arm IG), repeated every 3 weeks. The total number of cycles administered was 255 in the IG arm and 245 in the G arm; the median number of cycles was 3. In all, 145 patients (71 in arm IG and 74 in arm G) were enrolled; 60 and 70 patients from arms IG and G, respectively, were evaluable. A complete clinical response was achieved in three (4.3%) arm G patients; nine (15%) patients in arm IG and four (5.7%) in arm G achieved a partial response. The overall response rate was: arm IG 15% and arm G 10% (95% CI 5.96–24.04 and 95% CI 2.97–17.03, respectively; P=0.387). The median time to tumour progression was 2.8 months and 2.9 months and median survival time was 6.4 and 6.5 months for the IG and G arms, respectively. One-year survival was 24.3% for the IG arm and 21.8% for the G arm. No statistically significant difference was observed comparing gemcitabine monotherapy versus gemcitabine plus irinotecan in the treatment of advanced pancreatic cancer, with respect to overall and 1-year survival.
机译:我们的目的是确定吉西他滨单药治疗与吉西他滨加伊立替康相比在晚期或转移性胰腺癌中的缓解率以及中位生存期和总生存期。纳入经组织学或细胞学证实为腺癌且未接受化学疗法和放疗的患者。患者以一对一的比例进行中心随机分配,接受吉西他滨单药治疗(每4周在第1、8和15天(G组)接受900?mg?m?2)或吉西他滨(第1和8天)加伊立替康(第8天IG的剂量为300?mg?m?2),每3周重复一次,给药的总周期数在IG臂为255,在G臂为245;中位周期为3。全部入组145例患者(IG臂为71例,G臂为74例); IG和G臂分别为60例和70例,其中3例(4.3%)获得了完全的临床反应。 IG组的9例(15%)和G组的4例(5.7 %)达到了部分缓解,总缓解率为:IG组15%和G组10%(95%CI 5.96–24.04分别为95%CI 2.97–17.03; P = 0.387),IG和G组的中位肿瘤进展时间分别为2.8个月和2.9个月,中位生存时间分别为6.4和6.5个月。 IG臂为24.3 %,而2 G臂为1.8%。比较吉西他滨单药治疗与吉西他滨加伊立替康治疗晚期胰腺癌的总生存期和一年生存率无统计学差异。

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