新辅助与辅助膀胱热灌注化疗治疗高危非肌层浸润性膀胱癌的疗效对比
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  • 英文篇名:Effectiveness of Neoadjuvant and Adjuvant Bladder Intracavitary Hyperthermic Perfusion Chemotherapy(BHPC) on High-risk Non-muscle-invasive Bladder Cancer Patients
  • 作者:刘三河 ; 崔殿生 ; 贾全安 ; 邓康俐 ; 黄雷 ; 李有元 ; 魏少忠
  • 英文作者:LIU Sanhe;CUI Diansheng;JIA Quan'an;DENG Kangli;HUANG Lei;LI Youyuan;WEI Shaozhong;Department of Urology, Hubei Cancer Hospital;
  • 关键词:膀胱癌 ; 膀胱热灌注化疗 ; 吉西他滨
  • 英文关键词:Bladder cancer;;Bladder intracavitary hyperthermic perfusion chemotherapy;;Gemcitabine
  • 中文刊名:ZLFY
  • 英文刊名:Cancer Research on Prevention and Treatment
  • 机构:湖北省肿瘤医院泌尿外科;
  • 出版日期:2019-01-24 09:57
  • 出版单位:肿瘤防治研究
  • 年:2019
  • 期:v.46
  • 基金:国家自然科学基金(81700669);; 湖北省自然科学基金(2016CFB217)
  • 语种:中文;
  • 页:ZLFY201903011
  • 页数:4
  • CN:03
  • ISSN:42-1241/R
  • 分类号:63-66
摘要
目的探讨经尿道膀胱肿瘤电切术(TURBT)术前新辅助膀胱热灌注化疗对比术后辅助膀胱热灌注化疗治疗高危非肌层浸润性膀胱癌的疗效。方法收集经尿道膀胱肿瘤电切术术前或术后使用BR-TRG-Ⅱ型体腔热灌注治疗仪行吉西他滨膀胱热灌注化疗治疗高危非肌层浸润性膀胱癌患者40例,其中16例行术前(吉西他滨1000 mg,45℃,45 min)新辅助膀胱热灌注化疗3次,隔天一次,治疗结束后3~7天行经尿道膀胱肿瘤电切术,定义为新辅助组;另外24例患者先行TURBT手术,术后即刻或者隔天(吉西他滨1000 mg,45℃,45 min)行辅助膀胱热灌注化疗,定义为辅助组。记录并比较两组患者无疾病复发生存期(RFS)以及不良反应。结果全部40例患者均完成3次吉西他滨膀胱热灌注化疗,新辅助组患者中,完全缓解(p T0)11例(68.8%),部分缓解5例(31.2%)。新辅助组中位无复发生存期为54月,辅助组中位无复发生存期为45月,两者比较差异无统计学意义(P=0.3146)。两组患者不良反应可耐受。结论无论是新辅助还是辅助治疗,使用BR-TRG-Ⅱ型体腔热灌注治疗仪行吉西他滨膀胱热灌注化疗治疗高危非肌层浸润性膀胱癌安全有效。
        Objective To analyze the effectiveness of neoadjuvant and adjuvant bladder intracavitary hyperthermic perfusion chemotherapy(BHPC) on high-risk non-muscle-invasive bladder cancer(NMIBC)patients. Methods We included 40 patients with high-risk NMIBC who received BHPC treatment with a "BR-TRG-Ⅱ type high-precision hyperthermic intraperitoneal perfusion treatment system" before or after transurethral resection of the bladder tumor(TURBT). Among these patients, 16 patients received neoadjuvant BHPC treatment(gemcitabine 1000 mg three instillations every other day, 45℃, 45 min) before TURBT(neoadjuvant group) and 24 patients received adjuvant BHPC treatment(gemcitabine 1000 mg three instillations every other day, 45℃, 45 min) after TURBT(adjuvant group). Disease recurrence free survivals(RFS) and adverse effects were evaluated between both groups. Results A total of 40 patients completed three times of gemcitabine therapy. In neoadjuvant group, 11 patients(68.8%) showed a complete response(p T0) and 5 patients(32.2%) showed a partial response. The median RFS was 54 months. In adjuvant group,the median RFS was 45 months. The difference of survival rate between them was not statistically significant(P=0.3146). The incidence and severity of side effects were mild in both two groups. Conclusion BHPC on high-risk NMIBC patients using a "BR-TRG-Ⅱ type high-precision hyperthermic intraperitoneal perfusion treatment system" is safe and effective in both neoadjuvant and adjuvant settings.
引文
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