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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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) |
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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
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Department of Gynecologic Oncology, Zhejiang Cancer Hospital, Hangzhou 310022, China
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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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