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引用本文:闫鼎鼎,周建松,徐小仙,殷卓敏,刘南芳,袁淑慧,倪镌,李莉,楼寒梅.3种同步化疗方案在中晚期宫颈癌放疗中的疗效及不良反应[J].中国现代应用药学,2017,34(9):1317-1321.
YAN Dingding,ZHOU Jiansong,XU Xiaoxian,YIN Zhuomin,LIU Nanfang,YUAN Shuhui,NI Juan,LI Li,LOU Hanmei.Efficacy and Toxicity of Three Different Concurrent Chemoradiotherapy in Local Advanced Cervical Cancer[J].Chin J Mod Appl Pharm(中国现代应用药学),2017,34(9):1317-1321.
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3种同步化疗方案在中晚期宫颈癌放疗中的疗效及不良反应
闫鼎鼎, 周建松, 徐小仙, 殷卓敏, 刘南芳, 袁淑慧, 倪镌, 李莉, 楼寒梅
浙江省肿瘤医院妇瘤放疗科, 杭州 310022
摘要:
目的 比较3种同步化疗方案在中晚期宫颈癌放疗中的疗效及不良反应。方法 将符合入组标准的105例ⅡB-ⅢB中晚期宫颈癌患者随机分为DDP组、FP组、TP组,每组各35例,均行根治性放疗,DDP组放疗期间给予顺铂单药周疗,共4~5程,FP组给予氟尿嘧啶及顺铂联合化疗,间隔3周疗法,共2程,TP组给予紫杉醇及顺铂联合化疗,间隔3周疗法,共2程,对3组患者的疗效及不良反应分别进行记录。结果 根治性放疗结束1月后3组患者的完全缓解率(complete remission rate,CR)分别为88.6%,82.9%,82.9%,部分缓解率(partial remission rate,PR)分别11.4%,17.1%,11.4%;治疗结束3月后3组患者的CR率分别为97.1%,97.1%,94.3%,3组比较差异均无统计学意义。3组的2年总生存率分别为97.1%,85.7%,91.4%,2年的无瘤生存率分别为82.9%,85.7%,88.6%,差异均无统计学意义。主要近期不良反应为骨髓抑制和胃肠道反应,TP组3~4度白细胞减少及中性粒细胞减少的发生率最显著,FD组3~4度恶心、呕吐、腹泻及肠梗阻的发生率最显著,差异均有统计学意义(P<0.05),远期不良反应为放射性肠炎及放射性膀胱炎,3组的发生率均无统计学意义。结论 中晚期宫颈癌根治性放疗中3种同步化疗方案的近期疗效相似,2年的总生存率及无瘤生存率无差异,紫杉醇联合顺铂组的骨髓抑制最严重,氟尿嘧啶联合顺铂组的胃肠道反应最严重。
关键词:  宫颈癌  同步放化疗  顺铂  氟尿嘧啶  紫杉醇
DOI:10.13748/j.cnki.issn1007-7693.2017.09.022
分类号:R969.4
基金项目:浙江省医药卫生科技计划项目(2016KYA036);浙江省医药卫生科技平台项目(2017ZD012)
Efficacy and Toxicity of Three Different Concurrent Chemoradiotherapy in Local Advanced Cervical Cancer
YAN Dingding, ZHOU Jiansong, XU Xiaoxian, YIN Zhuomin, LIU Nanfang, YUAN Shuhui, NI Juan, LI Li, LOU Hanmei
Department of Gynecologic Oncology, Zhejiang Cancer Hospital, Hangzhou 310022, China
Abstract:
OBJECTIVE To observe the efficacy and toxicity of three concurrent chemotherapy regimens in the radiotherapy of local advanced cervical cancer. METHODS The 105 patients with FIGO stage IIB-IIIB cervical cancer were treated with concurrent chemoradiotherapy, and all cases were randomly divided into three groups, DDP group(35 cases) received cisplatin weekly for 4-5 cycles, FP group(35 cases) received fluorouracil and cisplatin combined chemotherapy every 3 weeks for 2 cycles, TP group(35 cases) received paclitaxel and cisplatin combined chemotherapy every 3 weeks for 2 cycles. Then compared acute adverse reaction and the efficacy of all patients. RESULTS The complete remission rates of the three groups were 88.6%, 82.9%, 82.9%, the partial remission rates were 11.4%, 17.1%, 11.4% at one month after radiotherapy, the complete remission rates were 97.1%, 97.1%, 94.3% at three months after radiotherapy, there was no significant difference(P>0.05). The 2-year overall survival rates were 97.1%, 85.7%, 91.4%, the 2-year disease-free survival rates was 82.9%, 85.7%, 88.6%, there was no significant difference. The main acute adverse reactions were bone marrow suppression and gastrointestinal reactions. Grade 3-4 leucopenia and neutropenia incidence was more common in paclitaxel and cisplatin group, Grade 3-4 nausea, vomiting, diarrhea and intestinal obstruction were more common in fluorouracil and cisplatin group (P<0.05). The main long-term adverse reactions were radiation enteritis and radiation cystitis, and the incidence of the three groups had no significant difference. CONCLUSION The short-term efficacy of the three concurrent chemotherapy for the treatment of advanced cervical cancer are similar. The 2-year overall survival rate and disease-free survival rate between three groups is similar. The paclitaxel and cisplatin group arise more severe bone marrow suppression. The fluorouracil and cisplatin group arise more severe gastrointestinal reactions.
Key words:  cervical cancer  concurret chemoradiotherapy  cisplatin  fluorouracil  paclitaxel
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