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GEMOX对比GX方案一线治疗晚期转移性胆系肿瘤的临床观察
引用本文:李嵘,秦叔逵,刘秀峰,龚新雷,华海清,王琳.GEMOX对比GX方案一线治疗晚期转移性胆系肿瘤的临床观察[J].肿瘤防治研究,2013,40(6):588-592.
作者姓名:李嵘  秦叔逵  刘秀峰  龚新雷  华海清  王琳
作者单位:210002 南京,南京解放军八一医院全军肿瘤中心
摘    要:目的观察吉西他滨联合奥沙利铂方案(GEMOX组)或希罗达(GX组)方案一线治疗晚期转移性胆系肿瘤(BTCs)的有效性及安全性。方法回顾性分析经病理及影像学检查确诊为原发性胆系肿瘤Ⅳ期的61例患者。其中,GEMOX方案为一线治疗的31例,GX方案为一线治疗的30例。GEMOX组:吉西他滨1 000 mg/m2静脉滴注d1、8,奥沙利铂 100 mg/m2静脉滴注d2。GX组:吉西他滨1 000 mg/m2静脉滴注d1、8;希罗达片1 250 mg/ m2 ,口服 2次/日 d1~14。两方案均21天为一周期。至少完成2周期化疗的患者进行疗效、不良反应评价,并分析生存情况。结果GEMOX组完全缓解(CR)2例、部分缓解(PR)6例、稳定(SD)15例,有效率(RR)为25.8%,疾病控制率(DCR)74.2%,中位疾病进展时间(mTTP)6.5月,中位总生存期(mOS)12月;GX方案组CR 1例、PR 5例、SD 16例,RR 20.0%,DCR 73.3%,mTTP为 6月,mOS 为10月。两组的RR、DCR、mTTP、mOS差异均无统计学意义(P>0.05)。两组Ⅲ度白细胞减少分别为6.5% vs. 6.7%,Ⅲ度血小板减少分别为6.5% vs. 3.3%,两组比较差异无统计学意义(P>0.05)。而外周神经炎以GEMOX组显著,手足综合征仅见于GX组。结论GEMOX和GX方案均可作为一线治疗晚期转移性BTCs的推荐方案,两组不良反应均较轻,耐受性好,具体实施应根据患者个体耐受情况及药物毒性进行选择。

关 键 词:胆系肿瘤  吉西他滨  奥沙利铂  希罗达  联合化疗  
收稿时间:2012-09-11

Clinical Observation of GEMOX or GX as First Line Regimen for Advanced Billiary Tract Carcinoma
LI Rong,QIN Shukui,LIU Xiufeng,GONG Xinlei,HUA Haiqing,WANG Lin.Clinical Observation of GEMOX or GX as First Line Regimen for Advanced Billiary Tract Carcinoma[J].Cancer Research on Prevention and Treatment,2013,40(6):588-592.
Authors:LI Rong  QIN Shukui  LIU Xiufeng  GONG Xinlei  HUA Haiqing  WANG Lin
Institution:Carcinoma Cancer Center of PLA,81st Hospital at Nanjing,Nanjing 210002,China
Abstract:ObjectiveTo observe the efficacy and safety of Gemcitabine combined with Oxaliplatin(GEMOX regimen) or Xeloda(GX regimen) as the first line regimen for patients with advanced biliary tract carcinoma(BTC).MethodsSixty-one patients with primary biliary tract carcinoma were confirmed by pathologic and imaging examination as IVB stage . GEMOX (n=31) was administrated as: gemcitabine 1 000 mg/m2  VD d1,8,oxaliplatin 100 mg/m2 VD d2; GX (n=30) as: gemcitabine  000 mg/m2  VD d1,8,Xeloda tablets 1 250 mg / m2  PO BID D1-14.Two egimens were repeated every 3 weeks. Response and toxicity were evaluated in patients who completed two cycles of chemotherapy at least.ResultsGEMOX group achieved 2 complete remission(CR),6 partial remission (PR),15stable disease(SD)and 8 progressive disease(PD)and GX group achieved 1CR,5PR, 16SD,and PD 8,. The overall response rate (RR) and disease control rate (DCR) in GEMOX group were 25.8% and 74.2% and in GX group 20.0% and 73.3%, respetivly. The median disease progress time (mTTP) and the median overall survival time (mOS) was 6.5 months and 12 months in GEMOX group and in GX group 6 months and 10 months, respetivly. There were no significant difference between the two groups for RR,DCR,mTTP and mOS (P>0.05).The most common toxicity in the GEMOX and GX regimens was myelosuppression, grade Ⅲ leukopenia was 6.5% and 6.7% respectively, and grade Ⅲ degree Thrombocytopenia was 6.5% and 3.3% respectively. Difference between two groups was not significant (P>0.05). But peripheral neuritis had increased prevalence in the GEMOX group, and hand-foot syndrome was found only in the GX group,ConclusionGEMOX and GX regimens could both be recommended as the first-line treatments for patients with advanced biliary tract carcinoma. Adverse reactions of two groups were mild and well tolerated. How to specifically use should be based on individual tolerance and drug toxicity.
Keywords:Billary tract carcinoma  Gemcitabine  Oxaliplation  Xeloda  Combined chemotherapy
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