首页> 外文期刊>Romanian reports in physics >Second-line chemotherapy with gemcitabine and oxaliplatin in combination with loco-regional hyperthermia (EHY-2000) in patients with refractory metastatic pancreatic cancer - preliminary results of a prospective trial
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Second-line chemotherapy with gemcitabine and oxaliplatin in combination with loco-regional hyperthermia (EHY-2000) in patients with refractory metastatic pancreatic cancer - preliminary results of a prospective trial

机译:吉西他滨和奥沙利铂联合局部局部热疗的二线化疗(EHY-2000)在难治性转移性胰腺癌患者中的作用-一项前瞻性试验的初步结果

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There is no standard treatment for second-line in patients with metastaticpancreatic cancer. The treatment with local hyperthermia (41"2 C) in order toenhance the activity gemcitabine-oxaliplatin on liver metastasis and primary advancedtumor was added as standard treatment. The primary objective was the response ratewhile the secondary objective were the safety of chemotherapy associated withhyperthermia and overall survival. There were 26 patients included, diagnosed withmetastatic pancreatic cancer with progressive disease after gemcitabine treatment. Thepatients were enrolled in the period January 2005 "May 2011. The patients receivedgemcitabine 1000 mg/msq IV and oxaliplatin 100 mg/msq IV day 1 (GEMOX)combined with locoregional hyperthermia days1, 3 and 5 all repeated at 14 days. From26 patients included, 19 patients had an evaluable response at the treatment. Thetoxicity of chemotherapy for these patients was related with chemotherapy (neutropeniagrade III "24%; anemia grade III "8%, thrombopenia grade III "6%; neurologictoxicity grade III "22%. Toxicity related to hyperthermia was: discomfort because ofbolus pressure (2%), pain related with position (12%), power related pain (2%). Rate ofresponse was stable disease 53%, partial response 18% and progression disease 29%.Progression-free-survival was 3.9 months. Overall survival was 8.9 months.
机译:转移性胰腺癌患者尚无标准的二线治疗方法。为了增强吉西他滨-奥沙利铂对肝转移和原发性晚期肿瘤的活性,增加了局部热疗(41“ 2 C)作为标准治疗。主要目标是缓解率,次要目标是化疗与高热相关的安全性和总体生存期为26例,经吉西他滨治疗后被诊断为转移性胰腺癌且进展期疾病。2005年1月至2011年5月入组。患者在第1天接受吉西他滨1000 mg / msq IV和奥沙利铂100 mg / msq IV(GEMOX )与局部热疗的第1天,第3天和第5天相结合,在第14天重复进行。包括26例患者,其中19例在治疗中有可评估的反应。这些患者的化疗毒性与化疗有关(中性粒细胞减少三级“ 24%;贫血三级” 8%,血小板减少症三级“ 6%;神经系统毒性三级” 22%。与高热相关的毒性是:由于推注压力引起的不适(2 %),与位置相关的疼痛(12%),与功率相关的疼痛(2%),稳定疾病的反应率为53%,部分反应的率为18%,疾病进展的率为29%,无进展生存期为3.9个月,总生存期为8.9个月。

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