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作 者:杜春霞[1] 马建辉[2] 寿建忠[2] 毕新刚[2] 鲁力[2] 周爱萍[1]
机构地区:[1]国家癌症中心/中国医学科学院北京协和医学院肿瘤医院肿瘤内科,北京1000210 [2]国家癌症中心/中国医学科学院北京协和医学院肿瘤医院泌尿外科,北京1000210
出 处:《癌症进展》2016年第8期766-769,共4页Oncology Progress
摘 要:目的:初步评价吉西他滨联合奥沙利铂(GEMOX)双周方案治疗尿路上皮癌的疗效和安全性。方法选取20例浸润性或转移性尿路上皮癌患者,患者均为男性,中位年龄62岁,其中6例超过70岁,7例接受过单侧肾切除术;辅助化疗6例,一线化疗14例。给予吉西他滨1000 mg/m2静脉滴注d1,奥沙利铂85 mg/m2静脉滴注d2;每2周为一个周期。评价患者近期疗效及不良反应,同时观察无进展生存期(PFS)或者无病生存期(DFS)以及总生存期(OS)。结果全部患者共接受GEMOX方案化疗106周期,中位化疗5周期。14例一线化疗患者中位随访24个月,12例死亡,中位PFS为5个月,中位OS为14个月;10例患者可评价客观疗效,PR 4例(40%),SD 4例(40%),PD 2例(20%)。6例辅助化疗患者中位随访51个月,1例复发死亡,5例无病生存,尚未到达中位DFS和OS。消化道反应和骨髓抑制是最常见的不良反应,中性粒细胞下降(15.8%)是最常见3~4级不良反应。结论GEMOX方案治疗尿路上皮癌耐受良好,在一线化疗中展现了较好的疗效,值得在老年患者或具有肾功能不全高危风险的患者中进一步研究。Objective To assess the efficacy and safety of biweekly regimen of gemcitabine combined with oxaliplat-in (GEMOX regimen) in urothelial carcinoma. Method 20 patients with invasive or metastatic urothelial carcinoma were enrolled in this study. All patients were male, with a median age of 62 years, 6 of them were over 70 years, and 7 pa-tients underwent unilateral nephrectomy; 6 patients had adjuvant chemotherapy, while 14 patients received GEMOX as first-line chemotherapy. GEMOX regimen: gemcitabine 1000 mg/m2 ivgtt, d1, oxaliplatin 85 mg/m2 ivgtt, d2, with 2 weeks as a cycle. Short-term response rate and adverse reactions were observed, and progression-free survival (PFS), dis-ease-free survival (DFS) and overall survival (OS) were also evaluated. Result A total of 106 cycles were completed, and the median number of cycles was 5. Patients who were given first-line chemotherapy had a median follow-up of 24 months, in which there were 12 cases of death, with a median PFS of 5 months, and the median OS was 14 months;Among the 10 evaluable cases, partial response (PR) was observed in 4 (40%), stable disease (SD) in 4 (40%), and pro-gression disease (PD) in 2 (20%). The median follow-up time was 51 months in adjuvant therapy group. One patient died of recurrence, 5 patients survived without disease, while the mPFS and the mOS were not reached. Digestive reactions and myelosuppression were the most common toxicities. Neutropenia (15.8%) was the most frequent adverse reaction of grade 3~4. Conclusion GEMOX showed an encouraging efficacy and a good safety profile as first-line chemotherapy in urothelial carcinoma, which merits further investigation in patients with urothelial carcinoma, especially in geriatric pa-tients or patients with high risk of renal dysfunction.
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