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同步整合加量新辅助放化疗用于局部晚期宫颈癌:单中心经验的长期结果

Neoadjuvant Chemoradiotherapy With Simultaneous Integrated Boost in Locally Advanced Cervical Cancer: Long Term Results of a Single-Center Experience.

作者信息

Nardangeli Alessia, Autorino Rosa, Boldrini Luca, Campitelli Maura, Reina Sara, Ferrandina Gabriella, Bizzarri Nicolò, Tagliaferri Luca, Macchia Gabriella, Valentini Vincenzo, Gambacorta Maria Antonietta

机构信息

UOC Radioterapia Oncologica, Dipartimento Diagnostica per Immagini, Radioterapia Oncologica ed Ematologia, Fondazione Policlinico Universitario Agostino Gemelli Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Roma, Italy.

Dipartimento Universitario di Scienze Radiologiche ed Ematologiche, Università Cattolica del Sacro Cuore, Roma, Italy.

出版信息

Front Oncol. 2022 May 5;12:883965. doi: 10.3389/fonc.2022.883965. eCollection 2022.

Abstract

Aim of this study was to analyze the efficacy and tolerability of simultaneous integrated boost volumetric modulated arc therapy (SIB-VMAT) associated with cisplatin-based chemotherapy in preoperative setting of patients with locally advanced cervical cancer (LACC). From June 2013 to September 2019, we analyzed patients with LACC who had undergone neoadjuvant chemoradiation (CRT). A radiation dose of 39.6 Gy, 1.8 Gy/fraction was delivered to the pelvis plus a radiation dose to the primary tumor delivered with SIB-VMAT strategy for a total of 50.6Gy, 2.3Gy/fraction in 25 fractions. Cisplatin-based chemotherapy was delivered combined with radiotherapy. Radical hysterectomy plus pelvic with or without aortic lymphadenectomy was performed within 7 to 8 weeks from CRT. One hundred forty-eight patients (median age: 49.5 years; FIGO stage IB2: 7, IIA: 8, IIB: 106, IIIA: 5; IIIB: 16; IVA: 5, IVB: 1; N0: 56, N1: 92) were analyzed. The treatment was well tolerated with good compliance: no grade 3/4 gastrointestinal or genitourinary toxicity was reported; grade 3 neutropenia was described in five cases. Pathological complete response (pCR) was documented in 68 cases (46%) and 32 patients (21.6%) had microscopic residual disease. Pathological nodal involvement was observed in 23 patients (15.5%). At median follow-up of 59 months (range: 27-100), the 3-year local control was 78.5%, whereas the 3-year metastasis-free survival was 70.5%. The 3-year overall survival rate was 89.0%. Neoadjuvant CRT with SIB-VMAT followed by radical surgery results in a high rate of pathologically assessed complete response and a very encouraging local control rate, with acceptable toxicity.

摘要

本研究的目的是分析同步整合加量容积调强弧形放疗(SIB-VMAT)联合基于顺铂的化疗方案在局部晚期宫颈癌(LACC)患者术前治疗中的疗效和耐受性。2013年6月至2019年9月,我们分析了接受新辅助放化疗(CRT)的LACC患者。盆腔接受39.6Gy的放射剂量,分1.8Gy/次,同时对原发肿瘤采用SIB-VMAT策略给予放射剂量,总计50.6Gy,分25次,每次2.3Gy。基于顺铂的化疗与放疗联合进行。在CRT后7至8周内进行根治性子宫切除术加盆腔淋巴结清扫术,可选择是否清扫主动脉旁淋巴结。共分析了148例患者(中位年龄:49.5岁;国际妇产科联盟(FIGO)分期:IB2期7例,IIA期8例,IIB期106例,IIIA期5例,IIIB期16例,IVA期5例,IVB期1例;N0期56例,N1期92例)。治疗耐受性良好,依从性佳:未报告3/4级胃肠道或泌尿生殖系统毒性;5例出现3级中性粒细胞减少。68例(46%)记录有病理完全缓解(pCR),32例(21.6%)有镜下残留病灶。23例(15.5%)观察到病理淋巴结受累。中位随访59个月(范围:27 - 100个月)时,3年局部控制率为78.5%,3年无转移生存率为70.5%。3年总生存率为89.0%。新辅助CRT联合SIB-VMAT后行根治性手术,病理评估完全缓解率高,局部控制率非常令人鼓舞,且毒性可接受。

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