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Chemoradiotherapy with or without induction chemotherapy for locally advanced pancreatic cancer: a UK multi-institutional experience.

机译:在局部晚期胰腺癌中进行或不进行诱导化疗的放化疗:英国的多机构经验。

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AIMS: The optimal management for patients with unresectable locally advanced adenocarcinoma of the pancreas (LAPC) is unclear. The aim of this study was to determine the outcome of patients treated with chemoradiotherapy (CRT) with or without induction chemotherapy. MATERIALS AND METHODS: We conducted a multi-centre retrospective analysis of 48 patients with biopsy-proven LAPC treated with CRT in four regional oncology centres in the UK between March 2000 and October 2007. The prescribed radiotherapy dose was 4500-5040 cGy in 25-28 fractions and was given concurrent with gemcitabine (n=37), gemcitabine/cisplatin (n=9), 5-fluorouracil (n=1) or capecitabine (n=1). RESULTS: Four patients (8.3%) did not complete the intended treatment due to CRT-related toxicities. The disease control rate (Objective response rate (ORR) and stable disease (SD)) was 81.3%. The median overall survival was 17 months (range 5-66 months). In subgroup analysis, a trend towards improved survival was seen in patients who completed the intended treatment (17.1 months vs 11.0 months, P=0.06) and in patients undergoing surgery (27 months vs 16 months, P=0.023). CONCLUSIONS: This is the largest reported series from the UK focussing on patients who received CRT for pancreas cancer. It shows that it is possible to deliver pancreatic CRT with acceptable toxicity. Induction chemotherapy followed by gemcitabine-based CRT shows promising activity and should be evaluated in phase III studies.
机译:目的:对于无法切除的局部晚期胰腺癌(LAPC)患者的最佳治疗方法尚不清楚。这项研究的目的是确定接受或不接受诱导化疗的放化疗患者的结果。材料与方法:我们对2000年3月至2007年10月在英国的四个区域肿瘤学中心对48例经活检证实的经CRT活检的LAPC患者进行了多中心回顾性分析。在25- 28馏分与吉西他滨(n = 37),吉西他滨/顺铂(n = 9),5-氟尿嘧啶(n = 1)或卡培他滨(n = 1)并用。结果:四名患者(8.3%)由于与CRT相关的毒性而未能完成预期的治疗。疾病控制率(客观缓解率(ORR)和稳定疾病(SD))为81.3%。中位总生存期为17个月(5-66个月)。在亚组分析中,在完成预期治疗的患者(17.1个月对11.0个月,P = 0.06)和接受手术的患者(27个月对16个月,P = 0.023)中观察到了生存改善的趋势。结论:这是英国报道的最大的系列,重点针对因胰腺癌接受CRT的患者。它表明可以以可接受的毒性递送胰腺CRT。诱导化疗后以吉西他滨为基础的CRT显示出有希望的活性,应在III期研究中进行评估。

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