宫颈癌的同步放化疗

早期宫颈癌的主要治疗方式是手术,而放疗是中晚期宫颈癌的主要治疗手段.近年来一系列随机分组研究表明,中晚期宫颈癌应用以顺铂为基础的同步放化疗较单纯放疗明显改善生存率,使死亡危险下降30%～50%.对具有高危因素的早期宫颈癌进行术后同步放化疗较单纯放疗、单纯化疗提高了疗效.至于放疗前新辅助化疗的疗效,目前研究结果表明未能改善生存.如何改进治疗,特别是选用放疗中联合应用的最佳化疗方案均需进一步研究.     

放疗联合卡培他滨同期治疗术后直肠癌疗效分析

目的探讨放疗联合卡培他滨同期治疗术后直肠癌的疗效和毒性。方法直肠癌术后患者67例,术后3～4周后先行改良的FOLFOX4方案化疗4次后行盆腔放疗,其中36例行单纯放疗,31例行同期放化疗。同期放化疗者从放疗的第1天开始给予卡培他滨825 mg/m2,2次/天,用至放疗结束。所有患者放疗结束后再用先前的化疗方案化疗4次。结果 67例患者中有66例完成了放疗。中位随访时间为26个月,有7例患者死亡,其中同期放化疗者中4例死亡,单纯放疗者中3例死亡。同期放化疗者中有1例盆腔复发,1例肝转移。单纯放疗者中有1例盆腔复发,2例肝转移和1例肺转移。结论直肠癌术后同期放化疗较单纯放疗有降低远处转移的趋势。     

局部晚期宫颈癌新辅助化疗近期疗效及生存研究

目的探讨新辅助化疗在局部晚期宫颈癌治疗中的近期疗效及5年生存情况。方法回顾性分析我院2000年1月-2004年1月手术治疗的193例局部晚期宫颈癌患者的病例资料,分为新辅助化疗（NACT）后手术组和直接手术组,比较两组的近期疗效、手术时间、术中出血量、术后留置尿管时间、术中及术后并发症、盆腔淋巴结转移、宫旁及切缘阳性率等。收集同期放疗病例,比较NACT后手术与直接手术、NACT后手术与放疗、NACT后手术＋放疗与手术＋放疗的5年生存率。结果NACT后手术组宫旁及阴道切缘阳性率〈直接手术组;两组淋巴结转移、手术时间、术中出血、术后留置尿管时间、术中术后并发症等的差异无统计学意义;NACT后手术组的5年生存率〉直接手术组和放疗组。结论NACT降低宫旁及阴道切缘阳性率,不降低盆腔淋巴结转移率,不增加术中出血、手术时间及术后并发症;NACT可将5年生存率提高到75％以上。     

早期宫颈癌术后辅助治疗疗效分析

目的:研究宫颈癌术后辅助治疗的选择与疗效.方法:回顾性分析159例宫颈癌根治术后辅助放疗加或不加化疗的患者治疗效果,选取130例同期行宫颈癌根治术的Ⅰb期及Ⅱa期未作术后辅助治疗患者作为对照组,进一步分析宫颈癌预后因素.159例患者中有87例放疗化疗综合治疗,72例单纯放疗.结果:289例患者总的5年生存率为89.3%,(单纯放疗组5年生存率88.9 % ,放疗化疗综合治疗5年生存率为 89.7%),对照组5年生存率72.9%.两者差异有显著性(P<0.05).结论:宫颈癌术后辅助治疗尤其对于盆腔淋巴结转移者有意义,临床和术后病理分期是术后辅助治疗的选择与疗效最主要的影响因素,不同病理类型及分级的宫颈癌术后辅助治疗可有不同的选择.     

Ia2-Ⅱa期宫颈癌术后盆腔小野放化疗取代盆腔标准野放疗的临床探究

目的:观察采用盆腔小野放化疗与盆腔标准野放疗治疗Ia2-Ⅱa期术后宫颈癌患者的生存率及不良反应。方法:选取2009年7月至2012年7月之间行广泛全子宫切除+盆腔淋巴结清扫后的Ia2-Ⅱa期且具有肿瘤复发中危因素行术后治疗的宫颈癌患者,随机分为两组:盆腔小野放化疗组、盆腔标准野放疗组。比较两组患者的生存率及不良反应。结果:采用盆腔小野放化疗组、标准放疗组的4年生存率分别为97.6%、92.9%,两组间比较差异无统计学意义（P＞0.05）。但在不良反应方面,盆腔小野放化疗组的直肠反应及泌尿道反应明显低于标准野放疗组,差异具有统计学意义（P＜0.05）。结论:盆腔小野放化疗组与盆腔标准野放疗组的4年生存率未见明显差异,因此采用盆腔小野放化疗对行根治性手术的Ia2-Ⅱa期宫颈癌患者中具有中度预后不良危险因素的患者是可行的,且采用盆腔小野放化疗的不良反应较标准放疗组明显低、患者生活质量明显提高。     

早期宫颈癌术后辅助治疗疗效分析

目的：研究宫颈癌术后辅助治疗的选择与疗效。方法：回顾性分析159例宫颈癌根治术后辅助放疗加或不加化疗的患者治疗效果,选取130例同期行宫颈癌根治术的Ⅰb期及Ⅱa期未作术后辅助治疗患者作为对照组,进一步分析宫颈癌预后因素。159例患者中有87例放疗化疗综合治疗,72例单纯放疗。结果：289例患者总的5年生存率为89.3%,（单纯放疗组5年生存率88.9%,放疗化疗综合治疗5年生存率为89.7%）,对照组5年生存率72.9%。两者差异有显著性（P〈0.05）。结论：宫颈癌术后辅助治疗尤其对于盆腔淋巴结转移者有意义,临床和术后病理分期是术后辅助治疗的选择与疗效最主要的影响因素,不同病理类型及分级的宫颈癌术后辅助治疗可有不同的选择。     

三种方案治疗Ⅰb2、Ⅱa2期宫颈癌患者生存状况及术后并发症的比较

目的 探讨单纯根治手术、新辅助化疗联合根治手术及同步放化疗联合根治手术方案对Ⅰb2、Ⅱa2期宫颈癌患者生存状况及术后并发症的影响。方法 回顾性分析140例Ⅰb2、Ⅱa2期宫颈癌患者临床资料，单纯根治手术治疗48例（A组），新辅助化疗联合根治手术治疗59例（B组），同步放化疗联合根治手术治疗33例（C组）。比较三组患者术中、术后临床指标、局部侵犯和淋巴结转移率、术后并发症发生率、中位总生存时间和术后1、2及3年生存率。结果 三组患者手术用时和总住院时间比较差异无统计学意义（P>0.05）；C组患者手术出血量、术后脉管和深肌层侵犯率及淋巴结转移率均显著低于A、B组（P<0.05）；三组患者术后神经侵犯率、术后并发症发生率、中位总生存时间和术后随访1、2及3年生存率比较差异均无统计学意义（P>0.05）。B组按术前治疗方式又分为放疗组（28例）、化疗组（13例）和放化疗组（18例），放疗组3年生存率明显高于化疗组与放化疗组（P<0.05）。结论 三组方案治疗Ⅰb2、Ⅱa2期宫颈癌生存状况和术后并发症风险相近；但同步放化疗联合根治手术有助于减轻手术创伤，降低术后局部侵犯和淋巴结转移率。     

复发宫颈癌近距离治疗进展

宫颈癌是女性常见的恶性肿瘤,其主要的治疗方式是手术和放疗。宫颈癌治疗后复发率高,复发后预后较差。复发宫颈癌可分为盆腔中央型、盆腔外周型和盆腔外复发,其治疗方案取决于患者初始治疗方式和复发位置。无放疗史的患者如有手术指征,可首选手术,也可联合放化疗±近距离治疗。放疗后盆腔中央复发的患者可选择盆腔廓清术±术中放疗,但其适应证具有高选择性,术后并发症发生率高,患者生存质量低。放疗后盆腔外周复发的患者可行再程外放疗和/或化疗。然而再程放疗的严重不良反应发生率高于初次放疗,立体定向体部放疗适应证较严格,对治疗者技术水平的要求也较高。近年来放疗技术更加精准,影像引导的近距离治疗如高剂量率组织间近距离治疗和放射性粒子植入获得了较好的疗效和安全性,为复发宫颈癌提供了新的治疗选择。本文就近年近距离治疗复发性宫颈癌的研究进展进行了梳理和总结。     

S-1联合奥沙利铂同步放疗食管癌术后局部淋巴结复发转移的临床观察

目的 探讨替吉奥联合奥沙利铂同步放疗食管癌根治术后局部淋巴结复发转移的临床疗效和相关不良反应.方法 回顾性分析经治的65例食管癌根治术后局部淋巴结复发转移患者,其中行同步放化疗33例(同步放化疗组),行单纯放疗32例(单纯放疗组),全部患者均给予三维适形放疗,分次剂量1.8～2.0 Gy/次,5次/周,总剂量60～ 64 Gy;同步放化疗组在放疗的第1周和第4周接受替吉奥联合奥沙利铂方案化疗(替吉奥40 mg/m2,早晚各1次口服,d1-14;奥沙利铂130 mg/m2,静脉滴注,d1).放疗结束后根据肿瘤消退情况两组均给予上述方案化疗2～4周期.比较两组患者治疗后的临床疗效、生存期及不良反应情况.结果 同步放化疗组和单纯放疗组近期总有效率(CR+ PR)分别为84.8％和59.4％,两组比较差异有统计学意义(P＜0.05).同步放化疗组和单纯放疗组患者1、2、3年无进展生存率分别为69.7％、36.3％、12.1％和40.6％、15.6％、0％,同步放化疗组和单纯放疗组患者中位无进展生存时间分别为14.6月和10.4月;同步放化疗组和单纯放疗组患者1、2、3年总生存率分别为75.8％、48.5％、24.2％和46.9％、28.1％、6.3％,同步放化疗组和单纯放疗组患者中位生存时间分别为21.5月和11.7月;两组患者无进展生存和总生存比较差异均有统计学意义(均P＜0.05).而同步放化疗组骨髓抑制、胃肠道反应、外周神经毒性、放射性食管炎及放射性肺炎的发生率与单纯放疗组比较差异均无统计学意义(均P＞0.05).结论 放疗同步替吉奥联合奥沙利铂方案化疗可提高食管癌术后局部淋巴结复发转移患者的近期疗效和远期生存率,不良反应可耐受.     

进展期胃癌根治术后放化疗与单纯化疗预后分析

目的 评价进展期胃癌根治术后放化疗与单纯化疗的疗效及不良反应。方法 搜集2004—2010年Ⅱ~Ⅳ(M₀)期胃癌根治术后病例共183例,其中术后放化疗64例、单纯化疗119例。分析二者生存及不良反应,分层分析二者在不同分期、不同淋巴结转移个数、不同手术方式(D₀、D₁、D₂术式)的生存差异。采用Kaplan-Meier法计算生存率并Logrank法检验和单因素分析,不良反应等行χ²检验。结果 随访率为87.8%,随访时间满3、5年例数分别为72、29例。术后放化疗和单纯化疗的1、3、5年生存率分别为86%、62%、55%和77%、53%、43%(P=0.079),3~4级胃肠道和血液学不良反应相似(P=0.363、0.617)。单因素分析显示Ⅲ_B~Ⅳ(M₀)期、D₀切除术、淋巴结转移个数>6个者放化疗比单纯化疗生存获益(P=0.022、0.025、0.021)。结论 胃癌根治术后放化疗有延长生存趋势,不良反应可耐受。Ⅲ_B~Ⅳ(M₀)期、D₀切除术、淋巴结转移个数>6个者可从放化疗中获益。     

Adjuvant concurrent chemoradiotherapy with intensity-modulated pelvic radiotherapy after surgery for high-risk, early stage cervical cancer patients

PURPOSE: This study was undertaken to assess local control and toxicity with adjuvant intensity-modulated radiotherapy (IMRT) and concurrent chemotherapy (CCRT) for early stage cervical cancer. PATIENTS AND METHODS: Between June 2004 and February 2007, 54 patients with early stage cervical cancer (stage IB-IIA) with high-risk factors for treatment failure after surgery were treated with adjuvant pelvic IMRT and CCRT. Adjuvant chemotherapy consisted of cisplatin (50 mg/m2) weekly for 4 to 6 courses. All the patients received 50.4 Gy of external beam radiotherapy with IMRT in 28 fractions and 6 Gy of high-dose rate vaginal cuff brachytherapy in 3 insertions. RESULTS: Adjuvant CCRT with IMRT provided good local tumor control in posthysterectomy cervical cancer patients with high-risk pathologic features. The 3-year locoregional control and disease-free survival were 93% and 78%, respectively. Histology and lymph node metastasis were indicators for disease-free survival. Low acute and chronic treatment-related toxicities were noted with IMRT. All the patients completed the radiotherapy treatment without any major toxicity. In terms of chronic toxicity, only 1 patient had grade 3 genitourinary toxicity and none had grade 3 gastrointestinal toxicity. CONCLUSION: Our results indicate that adjuvant CCRT with IMRT technique for adjuvant treatment of early stage cervical cancer is associated with excellent local control and low toxicity.     

同步放化疗对伴有盆腹腔淋巴结转移的宫颈癌患者疗效分析

目的 研究同步放化疗是否提高根治术后伴有盆腹腔淋巴结转移宫颈癌患者的生存。方法 收集2008-2011年间188例行宫颈癌根治术且术后病理伴有盆腹腔淋巴结转移的患者的临床资料,分析同步放化疗的疗效。结果 全组46例患者出现复发转移,单纯放疗组后腹膜、髂总及盆腔非髂总转移者的复发转移分别为4、5、11例(57.1%、55.6%、28.2%);同步放化疗组相应的复发转移分别为5、5、16例(62.5%、25%、15.2%)。与单纯放疗相比,同步放化疗能够明显改善盆腔非髂总、髂总淋巴结转移者的5年生存率(非髂总88.6%∶76.9%,P=0.003;髂总80.0%∶44.4%,P=0.041),而不能改善腹主动脉旁淋巴结转移者的5年生存率(50.0%∶42.9%,P=0.973)。淋巴结转移的部位及同步放化疗是总生存率的影响因素(后腹膜比盆腔非髂总HR=4.259,95%CI=1.700~10.671,P=0.002;髂总比盆腔非髂总HR=2.985,95%CI=1.290~6.907,P=0.011;同步放化疗比放疗:HR=0.439,95%CI=0.218~0.885,P=0.021)。结论 同步放化疗能改善盆腔淋巴结转移患者的生存,但不能改善腹主动脉旁淋巴结转移患者的生存。     

Feasibility and effectiveness of postoperative adjuvant concurrent chemoradiation therapy in Japanese patients with high-risk early-stage cancer of the uterine cervix

BACKGROUND: This study was undertaken to evaluate the feasibility and effectiveness of postoperative concurrent chemoradiation (CCRT) in patients with high-risk early-stage cervical cancer who were treated by radical hysterectomy and pelvic lymphadenectomy. METHODS: From July 2001 to September 2005, CCRT was performed in 37 patients who had undergone radical hysterectomy with pelvic lymph node dissection at Nagoya University Hospital. Adjuvant chemotherapy consisted of cisplatin (70 mg/m(2) on day 1) and 5-fluorouracil (5-FU; 700 mg/m(2) per day on days 1-4) every 4 weeks for a total of three cycles. Pelvic radiotherapy was started concurrently with the first cycle of chemotherapy. The radiation dose was 45 Gy in 25 fractions. A nonrandomized control group of 52 patients who had undergone radiation therapy alone after radical hysterectomy between 1991 and 2000 served for historical comparison. RESULTS: In the CCRT group, the incidences of grade 3/4 toxicities were 24.3% for neutropenia, 8.1% for nausea and vomiting, and 18.9% for diarrhea. The 5-year progression-free survival (PFS) rates in the CCRT group and control group were 89.2% and 69.2%, respectively (P = 0.0392). CONCLUSION: This study showed that adjuvant CCRT with cisplatin and 5-FU could be safely performed and improved the prognosis in Japanese patients with high-risk early-stage cervical cancer after radical hysterectomy.     

宫颈癌的术后放化疗

 宫颈癌术后有高危因素患者易局部复发。已经证实有高危因素患者术后行辅助放疗能提高局部控制率,但不能提高总生存率。有研究显示同步放化疗较单纯放疗能提高生存率,但血液及消化系统不良反应较重。调强放疗（IMRT）能提高靶区适形度及剂量,同时降低周围正常组织剂量,IMRT有较好的局部控制率及生存率。     

Preoperative prognostic variables and the impact of postoperative adjuvant therapy on the outcomes of Stage IB or II cervical carcinoma patients with or without pelvic lymph node metastases: an analysis of 891 cases

BACKGROUND: The purpose of this study was to investigate pretreatment variables that could predict prognosis and to evaluate the impact of postoperative adjuvant therapy on the outcomes of patients with Stage IB or II cervical carcinoma with or without pelvic lymph node metastases. METHODS: Eight hundred ninety-one patients with Stage IB or II cervical carcinoma who underwent radical hysterectomy and bilateral pelvic lymphadenectomy as primary treatment at a single institution were analyzed. Potential prognostic variables were studied. RESULTS: Among the variables that could be assessed before treatment, depth of cervical stromal invasion (determined by magnetic resonance imaging), clinical stage, tumor size, grade of differentiation, and DNA index (determined by flow cytometry) were independent predictors of outcome in multivariate analysis using a Cox regression model. Three distinct prognostic groups (low, intermediate, and high risk) were defined using these variables. Five-year recurrence free survival (RFS) rates for the low, intermediate, and high risk groups were 94.6%, 82.7%, and 62.3%, respectively (P = 0.0001), and overall survival (OS) rates were 98.4%, 84.5%, and 68.7%, respectively (P = 0.0001). Among patients with pelvic lymph node metastases who were free of parametrial extension, those who received postoperative chemotherapy or chemoradiotherapy had significantly better RFS (P = 0.017) and OS (P = 0.043) than those who received no adjuvant therapy. Among patients without pelvic lymph node metastases but at high risk of recurrence, those who received adjuvant radiotherapy had significantly better RFS (P = 0.015) and marginally improved OS (P = 0.087) compared with those who received no adjuvant therapy. CONCLUSIONS: A model containing assessable pretreatment variables for predicting the prognoses of patients with early stage cervical carcinoma was formulated. Subsets of patients for whom postoperative chemotherapy or radiotherapy might be beneficial were identified. The data from this retrospective review may be useful when future prospective trials of the treatment of early stage cervical carcinoma are designed.     

Prognostic factors affecting the outcome of early cervical cancer treated with radical hysterectomy and post-operative adjuvant therapy

The purpose of this study is to investigate the clinical and histological features that may affect the survival of the patients and to evaluate the impact of post-operative adjuvant therapy on the outcomes of patients with stage IB and IIA carcinoma of the cervix. From August 1998 to January 2005, 140 patients with International Federation of Gynecology and Obstetrics stage IB and IIA cervical cancer were treated with radical hysterectomy and post-operative pelvic radiation therapy with or without chemotherapy. The median age was 55 years (range, 29-86 years). Seventy-six patients had stage IB and 64 patients had stage IIA disease. Tumour size was <4 cm in 96 patients and > or = 4 cm in 44 patients. One hundred and eleven patients had histology of squamous cell carcinoma, 12 patients has adenocarcinoma and 17 patients had other histologic types. Depth of stromal invasion was <2/3 in 20 patients and > or = 2/3 in 120 patients. Twenty-three patients had parametrial invasion and 117 patients had no parametrial invasion. Thirteen patients had lymphovascular space invasion and 127 had no lymphovascular space invasion. Nine patients had positive surgical margin and 131 patients had negative margin. Twenty-seven patients had pelvic lymph node metastasis and 113 patients had no pelvic lymph node metastasis. Seventy-five patients received concurrent chemoradiotherapy and 65 patients received radiotherapy alone. The 5-year overall survival (OAS) and disease-free survival were 83% and 72% respectively. In the log rank test, tumour size (P = 0.0235), pararmetrial invasion (P = 0.0121), pelvic lymph node metastasis (P < 0.0001) and adjuvant chemotherapy + radiotherapy (P = 0.0119) were significant prognostic factors for OAS, favouring tumour size <4 cm, absence of parametrial invasion and pelvic lymph node metastasis, and those who received adjuvant chemoradiotherapy. The patients who received radiation with concomitant chemotherapy had a 5-year OAS rate of 90% versus those who received radiotherapy alone, with a rate of 76%. For patients with high-risk early stage cervical cancer who underwent a radical hysterectomy and pelvic lymphadenectomy, adjuvant chemoradiotherapy resulted in better survival than radiotherapy alone. The addition of weekly cisplatin to radiotherapy is recommended. The treatment-related morbidity is tolerable.     

老年宫颈癌患者术后复发的高危因素及其病理特征

目的:探讨分析老年宫颈癌患者术后复发高危因素及其病理特征。方法:回顾性分析2011年3月至2015年6月我院收治的老年宫颈癌（I-IIa期）并行宫颈癌根治术的338例患者临床资料,将术后复发患者56例作为复发组,其余未复发患者282例作为对照组,对可能影响患者术后复发的各因素进行单因素及多因素Logistic回归分析。结果:对患者进行术后随访,术后复发56例,术后复发率16.57%,其中鳞癌患者46例（82.14%）、非鳞癌患者10例（17.86%）。单因素分析结果显示,临床分期、肿瘤大小、组织分化程度、盆腔淋巴结转移、宫颈浸润深度、术后放疗、术后化疗以及术前SCC表达对老年宫颈癌患者术后复发有显著影响（P＜0.05）。多因素Logistic回归分析结果显示,盆腔淋巴结转移、临床分期、宫颈浸润深度、术后化疗以及SCC表达情况进入回归模型（P＜0.05）。结论:盆腔淋巴结转移、临床分期高、宫颈浸润深、术前SCC表达异常是老年宫颈癌患者术后复发的独立危险因素,而术后化疗是老年宫颈癌患者术后复发的保护因素。     

新辅助化疗后根治性手术与同步放化疗在局部晚期宫颈癌的远期疗效评价

目的本研究的目的是比较ⅠB2-ⅡB期局部晚期宫颈癌新辅助化疗后根治性手术与同步放化疗的远期生存情况。方法回顾性分析从2000年1月—2004年12月间ⅠB2-ⅡB期局部晚期宫颈癌共222例,将其分为二组：新辅助化疗＋根治性全子宫切除术＋盆腔淋巴结切除术共155例;同步放化疗组67例。所有患者最长随访时间为114个月,最短随访时间为54个月,中位随访时间为72．6个月。且对所有可能影响无瘤生存时间和总生存时间的高危因素进行评估。结果本研究中位随访时间为72．6个月,新辅助化疗后根治性手术组和同步放化疗组5年无瘤生存率分别是88．39％和70．94％,两组比较有统计学意义（P：0．006）;而5年总生存率分别为88．52％和72．91％,两组比较有统计学意义（P=0．0004）。在Cox风险回归模型中,调整宫颈癌患者的年龄、病理分型后,结果显示：接受新辅助化疗后根治性手术组和同步放化疗组治疗的宫颈癌患者5年无瘤生存时间有明显差异（HR：2．765,95％CI：1．446—5．288,P=0．0021）;在5年总生存时间上也有显著性差异（HR=3．516,95％CI：1．822—6．784,P=0．0002）。结论本研究ⅠB2-ⅡB期局部晚期宫颈癌新辅助化疗后根治性手术组在无瘤生存时间和总生存时间方面显著优于同步放化疗组。     

有高危因素的早期宫颈癌患者术后紫杉醇联合卡铂同期化放疗的疗效和安全性观察

目的评价紫杉醇联合卡铂同期放疗(CCRT)在治疗有高危因素早期宫颈癌术后的疗效和毒副反应。方法收集本科2008年7月1日至2011年6月30日收治ⅠB1～ⅡB宫颈鳞癌根治术后有高危因素的患者54例,其中行同期化放疗15例,39例行序贯放疗。同期化疗方案为紫杉醇(135 mg/m~2)联合卡铂(AUC=5)于放疗第一周进行一个疗程。辅助化疗方案同同期化疗,于放疗结束后开始,每21天一个疗程。比较同期化放疗和序贯放疗的复发率、无进展生存期(PFS)和总生存期(OS)以及急性期和晚期不良反应。结果 54例患者均按计划完成治疗,同期化放疗的中位放疗剂量50 Gy(46～52 Gy,每次2 Gy)和人均化疗次数4次(3～5次)与序贯放疗相似(P=0.60和P=0.34)。在中位随访20个月(8～43个月)期间发现,同期化放疗较序贯放疗能减少局部复发率(0/15 vs 9/39,P=0.04),而两组无进展生存期(log-rank,P=0.26)和总生存期(log-rank,P=0.51)相似。同期化放疗患者出现3～4级血液学不良反应比例高于序贯放疗(4/15 vs 1/39,P=0.03),而3级胃肠道急性不良反应相似(4/15 vs 5/39,P=0.22),随访期间两组患者未发现3～4级晚期不良反应。结论紫杉醇联和卡铂的同期化放疗能减少有高危因素的早期宫颈癌术后患者局部复发,并有较好耐受性。