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吉西他滨联合顺铂治疗肾移植术后并发尿路上皮癌的初步探讨
引用本文:田野,肖荆,朱一辰,张建,侯海军,王志鹏,郭宇文,杨培谦.吉西他滨联合顺铂治疗肾移植术后并发尿路上皮癌的初步探讨[J].现代泌尿外科杂志,2014(12):780-783.
作者姓名:田野  肖荆  朱一辰  张建  侯海军  王志鹏  郭宇文  杨培谦
作者单位:首都医科大学附属北京友谊医院泌尿外科,北京100050
基金项目:首都卫生发展科研专项项目基金(No.2011-2002-05)
摘    要:目的观察肾移植术后并发尿路上皮癌患者行静脉化疗的副作用和临床疗效。方法回顾分析7例肾移植受者并发尿路上皮癌的患者接受吉西他滨联合顺铂方案(GC)静脉化疗的临床资料,患者均为女性,年龄范围32~67岁。肾盂、输尿管及膀胱多发癌4例,肾盂癌2例,膀胱癌1例。1例患者在术前接受新辅助化疗,其余6例为术后辅助化疗,化疗方案为:吉西他滨700~800mg/m2第1、8、15天静脉滴注,顺铂50~60mg/m2第2天静脉滴注。每4周重复一次,共2~4个周期,7例患者共接受14个周期化疗。结果化疗药的近期毒副反应主要表现为血液学毒性7例(100%)、消化道反应5例(71%)、脱发2例(28%)、尿蛋白1例(14%),化疗1个周期后出现移植肾功能受损1例(14%)。所有患者随访2~11个月:其中1例患者对侧肾盂出现新的尿路上皮癌,1例患者腰大肌转移灶增大,病情恶化后死亡;其余5例患者近期随访无明显异常。结论肾移植受者合并浸润性尿路上皮癌可选择GC方案静脉化疗,但化疗药和免疫抑制剂的同时作用常导致较严重骨髓抑制,需要减少化疗药用量,并进一步调整免疫抑制剂,及时给予升白细胞和血小板治疗,患者可以基本耐受毒副作用,但远期疗效还需进一步观察。

关 键 词:肾移植  尿路上皮癌  静脉化疗  吉西他滨  顺铂

Gemicitabine combined with cisplatin for urothelial carcinoma in renal transplant recipients
TIAN Ye,XIAO Jing,ZHU Yi-chen,ZHANG Jian,HOU Hai-jun,WANG Zhi-peng,GUO Yu-wen,YANG Pei-qian.Gemicitabine combined with cisplatin for urothelial carcinoma in renal transplant recipients[J].Journal of MOdern Urology,2014(12):780-783.
Authors:TIAN Ye  XIAO Jing  ZHU Yi-chen  ZHANG Jian  HOU Hai-jun  WANG Zhi-peng  GUO Yu-wen  YANG Pei-qian
Institution:(Department of Urology,Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China)
Abstract:Objective To evaluate the clinical efficacy and side effects of intravenous chemotherapy in renal transplant recipients with urothelial carcinoma .Methods A total of 7 female renal transplant recipients aged 32-67 years with concur‐rent urothelial carcinoma receiving gemcitabine combined cisplatin (GC) scheme .Of all patients ,one received neoadjuvant chemotherapy and others chemotherapy after resection of tumors . The chemotherapy was:gemcitabine 700 -800 mg/m2 , ivgtt ,d1 ,d8 ,d15 ,cisplatine 50‐60 mg/m2 ivgtt ,d2 .Patients received the next chemotherapy cycle after 2 weeks of interval and a total of 2 to 4 cycles ,and altogether 14 cycles of chemotherapy were finished .Results The short‐term toxicity includ‐ed hematology toxicity 100% (7/7) ,digestive discomfort 71% (5/7) ,hair loss 28% (2/7) ,and proteinuria 14% (1/7) .The function of transplant kidney was impaired in one patient after one cycle of chemotherapy .During the follow‐up of 2 to 11 months ,new urothelial carcinoma appeared in one case in the off side of the renal pelvis and one patient died of metastasis in the psoas major .No obvious abnormalities were found in the other 5 patients . Conclusions Renal transplant recipients with muscle invasive urothelial carcinoma can choose GC scheme of intravenous chemotherapy ,but the effect of chemothera‐peutic drugs and the immune inhibitors often leads to severe myelosuppression .The dosage of the chemotherapeutic drugs and immune inhibitors should be reduced and decrease of white blood and platelets should be controlled in time .With careful man‐agement ,patients can tolerate side effects ,but the long‐term effect still needs further observation .
Keywords:renal transplantation  urothelial carcinoma  intravenous thermotherapy  gemcitabine  cisplatine
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