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作 者:魏艳红[1] 杨洁[1] 张尚暖[1] 祝倩倩[1] 张君莹[1] 韩正祥[1]
机构地区:[1]徐州医学院附属医院肿瘤科,江苏徐州221002
出 处:《徐州医学院学报》2013年第9期580-582,共3页Acta Academiae Medicinae Xuzhou
基 金:江苏省卫生厅医学科技发展基金会临床肿瘤学科研课题(P200942);徐州医学院课题(08KJ53)
摘 要:目的 评价吉西他滨(GEM)联合奥沙利铂(L-OHP)一线治疗晚期胆囊癌的近期疗效和毒副反应.方法 晚期胆囊癌21例.GEM 800 mg/m^2,第1、8天静脉给药;L-OHP 85 mg/m^2,第1天静脉给药;21天为1个疗程.2个疗程后评价患者的疗效、KPS评分、临床受益反应(CBR)、毒副反应等.结果 完全缓解(CR)0例,部分缓解(PR)5例,稳定(SD)7例,进展(PD)9例,总有效率(CR+PR)为23.8%,CBR为57.1%.化疗前后KPS评分差异无统计学意义(P>0.05).毒副反应主要为骨髓抑制(11例)、胃肠道反应(8例)、神经病变(3例).结论 GEM联合L-OHP一线治疗晚期胆囊癌近期疗效较好,毒性反应较轻,老年患者依从性好.Objective To evaluate the efficacy and toxicity of combination chemotherapy with gemcitabine and ox- aliplatin (GEMOX) as first - line therapy (GEMOX) for patients with advanced gall bladder cancer. Methods 36 eld- erly patients with advanced gall bladder cancer received gemcitabine 800 mg/m^2 ( day 1 and 8 ) and oxaliplatin 85 mg/m2 ( day 1 ) , every 3 weeks and at least 2 cycles. The evaluation was performed after the chemotherapy for 2 cycles. 36 patients were evaluable for efficacy, physical fitness score (KPS) , clinical benefit response (CBR) ,and toxicity, etc. Resuits No complete remission (CR) was observed. Partial remission (PR) was observed in 5 cases, stable disease (SD) in 7 cases and progressive disease (PD) in 9 cases. The objective response rate (defined as CR + PR) was 23.8% (5/21 ) and C BR was 57.1%. KPS score difference was not statistically significant (P 〉 0.05 ) before and after chemotherapy. The main adverse effects were : myelosuppression ( 11 cases), gastrointestinal reactions ( 8 cases) and neurosensory toxicity (3 cases). Conclusion Oxaliplatin plus gemeitabine first - line therapy for the treatment of ad- vanced biliary tract carcinoma has good short -term effect with mild adverse effects and are well tolerated in elderly pa- tients.
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