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首页> 外文期刊>Cancer: A Journal of the American Cancer Society >Neoadjuvant Gemcitabine, Docetaxel, and Capecitabine Followed by Gemcitabine and Capecitabine/Radiation Therapy and Surgery in Locally Advanced, Unresectable Pancreatic Adenocarcinoma
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Neoadjuvant Gemcitabine, Docetaxel, and Capecitabine Followed by Gemcitabine and Capecitabine/Radiation Therapy and Surgery in Locally Advanced, Unresectable Pancreatic Adenocarcinoma

机译:Neoadjuvant Gemcitabine,Docetaxel和Capecitabine随后是吉西滨和Capecitabine /放射治疗和手术在当地先进,不可切除的胰腺癌腺癌

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BACKGROUND: This prospective study was undertaken to assess toxicity, resectability, and survival in pancreatic adenocarcinoma patients presenting with locally advanced, unresectable disease treated with neoadjuvant gemcitabine, docetaxel, and capecitabine (GTX) and gemcitabine and capecitabine (GX)/radiation therapy (RT). METHODS: All patients presenting to the Pancreas Center were evaluated for eligibility. Forty-five patients (mean age, 64 years; range, 44-83 years)-34 patients deemed unresectable because of arterial involvement and 11 patients deemed unresectable because of extensive venous involvement-were treated with 6 cycles of GTX. Those with arterial involvement were treated with GX/RT after chemotherapy. RESULTS: The GTX and GX/RT treatments were tolerated with the expected drug-related toxicities. There were no bowel perforations, cases of pancreatitis, or delayed strictures. Among those with arterial involvement, 29 underwent subsequent resection, with 20 (69%) achieving R0 resections. All 11 patients with venous-only involvement underwent resection, with 8 achieving R0 resections and 3 achieving complete pathologic responses. For the arterial arm, the 1-year survival rate was 71% (24 of 34 patients), and the median survival was 29 months (95% confidence interval, 21-38 months). Thirteen patients (38%) have not relapsed (range, 5-491 months). For the venous arm, the median survival has not been reached at more than 42 months. Six patients (55%) in the venous arm did not experience recurrence (range, 6.2-421 months). CONCLUSIONS: GTX plus GX/RT is an effective neoadjuvant regimen that can be safely administered to patients up to at least the age of 83 years. It is associated with a high response rate, a high rate of R0 resections, and prolonged overall survival
机译:背景:该前瞻性研究是为了评估胰腺腺癌患者的毒性,重新入心和生存,呈现与Neoadjuvant Gemcitabine,Docetaxel和Capecitabine(GTX)和吉西他滨和Capecitabine(GX)/放射治疗(Rt )。方法:评价所有患者给胰腺的患者进行评估。四十五名患者(平均年龄,64岁;范围,44-83岁)-34患者由于动脉受累,11名患者由于广泛的静脉受累而被视为不可切除的患者 - 用6次GTX治疗。在化疗后,用Gx / Rt治疗动脉凋亡的人。结果:通过预期的药物相关毒性耐受GTX和GX / RT治疗。没有肠穿孔,胰腺炎病例或延迟狭窄。在有动脉累及的人中,29例后续切除,20(69%)实现R0切除术。所有11名患者患有静脉受累的患者接受了切除术,8例达到R0切除术和3达到完全病理反应。对于动脉臂,1年生存率为71%(34名患者中的24例),中位存活率为29个月(95%置信区间,21-38个月)。十三个患者(38%)尚未复发(范围,5-491个月)。对于静脉臂,在超过42个月内尚未达到中位生存率。静脉臂的六名患者(55%)没有经历复发(范围,6.2-421个月)。结论:GTX加GX / RT是一种有效的新辅助方案,可以安全地向患者安全地施用至少83岁。它与高响应速率,高率的R0切除率相关,延长了整体生存率

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