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首页> 外文期刊>Investigational new drugs. >Second-line treatment with oxaliplatin, leucovorin and 5-fluorouracil in gemcitabine-pretreated advanced pancreatic cancer: A phase II study.
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Second-line treatment with oxaliplatin, leucovorin and 5-fluorouracil in gemcitabine-pretreated advanced pancreatic cancer: A phase II study.

机译:奥沙利铂,亚叶酸钙和5-氟尿嘧啶在吉西他滨预处理的晚期胰腺癌中的二线治疗:II期研究。

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Study objectives: The present study was conducted to evaluate the efficacy and safety of the combination of Oxaliplatin, Leucovorin and 5-FU as second line therapy, following relapse to Gemcitabine, in patients with advanced adenocarcinoma of the pancreas. Patients and methods: Patients with advanced pancreatic cancer previously treated with Gemcitabine were included in the study. All patients had histologically or cytologically confirmed adenocarcinoma of the pancreas that was unresectable, locally advanced or metastatic. Treatment consisted of Oxaliplatin 50 mg/m(2) (2-hour iv infusion), followed by Leucovorin 50 mg/m(2) (i.v. bolus) and 500 mg/m(2) 5-FU (1-hour iv infusion), administered weekly, until unacceptable toxicity or disease progression. Objective tumour response and toxicity were evaluated according to World Health Organisation (WHO) criteria. Results: A total of 30 patients, 20 men and 10 women, median age 63 years (range 52-71 years) and Karnofsky Performance Status (PS) of >/=50 enteredthe study. The majority of patients (96%) had locally advanced disease. A total of 380 doses of chemotherapy were delivered, a median of 12 doses per patient. Partial responses were observed in 7 patients (PR 23.3%), stable disease in 9 (SD 30.0%), while 14 patients progressed (PD 46.7%). Improved PS was observed in 18 (42.8%) patients. Patients that had responded to first-line Gemcitabine treatment were found more likely to respond or stabilize their disease with second-line treatment. The median duration of response was 22 weeks, and median overall survival was 25 weeks, Grade 3/4 toxicity expressed per chemotherapy dose included leukopenia 16%, anemia 3.2%, thrombocytopenia 3.2%, diarrhea 14.2%, fatigue 16.1% and neurotoxicity 4.2%. Eight patients (27%) suffered a febrile neutropenic event managed successfully with oral antibiotic home therapy, while 17 patients required G-CSF support. There were no treatment related deaths. Conclusions: The combination of Oxaliplatin, Leucovorin and 5-FU was tolerated with manageable toxicity, offering encouraging activity as second-line treatment of patients with advanced or metastatic pancreatic adenocarcinoma, previously treated with Gemcitabine. Additional studies are warranted with this regimen in Gemcitabine relapsed pancreatic cancer patients.
机译:研究目的:本研究旨在评估吉西他滨复发后,奥沙利铂,白细胞素和5-FU联合作为二线治疗对晚期胰腺癌患者的疗效和安全性。患者和方法:该研究包括先前接受吉西他滨治疗的晚期胰腺癌患者。所有患者均经组织学或细胞学检查证实为不可切除,局部晚期或转移性胰腺癌。治疗方法包括:奥沙利铂50 mg / m(2)(静脉输注2小时),然后是白叶素50 mg / m(2)(静脉推注)和500 mg / m(2)5-FU(1小时静脉输注) ),每周给药一次,直到出现不可接受的毒性或疾病进展为止。根据世界卫生组织(WHO)的标准评估客观的肿瘤反应和毒性。结果:总共30例患者,其中20例男性和10例女性,中位年龄63岁(范围52-71岁),Karnofsky行为状态(PS)> / = 50。大多数患者(96%)患有局部晚期疾病。总共进行了380剂化疗,每位患者中位数为12剂。在7例患者中观察到部分缓解(PR 23.3%),在9例患者中发现稳定的疾病(SD 30.0%),而14例进展了(PD 46.7%)。在18名(42.8%)患者中观察到PS改善。发现对吉西他滨一线治疗有反应的患者更可能对二线治疗有反应或稳定其疾病。中位缓解时间为22周,中位总生存期为25周,每化疗剂量表达的3/4级毒性包括白细胞减少症16%,贫血3.2%,血小板减少症3.2%,腹泻14.2%,疲劳16.1%和神经毒性4.2% 。 8例患者(27%)通过口服抗生素家庭疗法成功治疗了发热性中性粒细胞减少症,而17例患者需要G-CSF支持。没有与治疗有关的死亡。结论:奥沙利铂,白细胞介素和5-FU的组合具有可控的毒性,可作为以前用吉西他滨治疗的晚期或转移性胰腺腺癌的二线治疗提供令人鼓舞的活性。对于吉西他滨复发的胰腺癌患者,需要对该方案进行进一步的研究。

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