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吉西他滨和顺铂同步化疗(CGP)联合调强放疗治疗局部晚期宫颈癌的耐受性、疗效及可行性

Tolerability, Efficacy and Feasibility of Concurrent Gemcitabine and Cisplatin (CGP) Combined With Intensity Modulated Radiotherapy for Loco-Regionally Advanced Carcinoma of the Cervix.

作者信息

Drokow Emmanuel Kwateng, Zi Liu, Qian Han, Xu Lanlan, Foli Francis, Ahmed Hafiz Abdul Waqas, Akpabla Gloria Selorm, Wu Guangyin, Agyekum Emmanuel Bamfo, Gao Weihua, Deku Marie-Anne, Song Juanjuan, Sun Kai

机构信息

Department of Radiation Oncology, Zhengzhou University People's Hospital & Henan Provincial People's Hospital 450003, China.

Department of Radiation Oncology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, China.

出版信息

J Cancer. 2020 Feb 19;11(9):2632-2638. doi: 10.7150/jca.40276. eCollection 2020.

Abstract

Gemcitabine and cisplatin combined with conventional radiotherapy in treating patients with cervical cancer, resulted in a favourable conclusion but accompanied with high toxicity. The objective of our research was to assess the tolerability, efficacy and feasibility of dual chemotherapy in addition to image-guided adaptive brachytherapy and highly conformal external beam radiation therapy. From June 2011 to November 2013, 81 cervical cancer patients with FIGO stage IB2-IIIB medical records were retrospectively reviewed. All patients received whole pelvic radiotherapy (WPRT) to a total dose of 50.4 Gy/ 1.8 Gy Chemoradiotherapy prescription objectives were: concurrent gemcitabine (125 mg/m) and cisplatin (30 mg/m) during the 6 weeks of external beam radiation therapy (EBRT) followed by two cycles of gemcitabine (1 g/m, d1, d8) and cisplatin (25 mg/m d1-d3) on the tenth week. External beam radiotherapy was followed by image-guided brachytherapy of 24 Gy/ 4 fractions. Version 4 of the common terminology criteria for adverse events (CTCAE v 4.0) was used in grading the toxicities. Sixty-nine patients obtained complete response (CR), six had a partial response (PR), and five patients had stable disease (SD). The disease control rate (DCR= SD and ORR) and overall response rate (ORR= PR, CR or PR) were 92.6% and 85.2% respectively. The 3-year and 5-year estimated overall survival (OS) was 75.4% and 66.3%, and the 3-year and 5-year estimated progression-free survival (PFS) were 78.2% and 65.4%. The median PFS time and OS time were 36.8 months and 45.5 months, respectively. Distance metastasis was evident in the lung (3 patients), pelvic wall (2 patients), liver (3 patients) and bone (2 patients). Six (6) had a local relapse, and two (2) patients had local relapse plus simultaneous systemic metastatic tumour. Unlike past results, gemcitabine and cisplatin appear to be tolerable, efficient and feasible when combined with conformal radiotherapy.

摘要

吉西他滨和顺铂联合传统放疗治疗宫颈癌患者,虽得出了有利的结论,但伴有高毒性。我们研究的目的是评估双药化疗联合图像引导自适应近距离放疗和高剂量适形外照射放疗的耐受性、疗效和可行性。回顾性分析了2011年6月至2013年11月期间81例国际妇产科联盟(FIGO)分期为IB2-IIIB期的宫颈癌患者的病历。所有患者均接受全盆腔放疗(WPRT),总剂量为50.4 Gy/1.8 Gy。放化疗处方目标为:在6周的外照射放疗(EBRT)期间同步给予吉西他滨(125 mg/m²)和顺铂(30 mg/m²),随后在第10周给予两个周期的吉西他滨(1 g/m²,d1、d8)和顺铂(25 mg/m²,d1-d3)。外照射放疗后进行图像引导的近距离放疗,剂量为24 Gy/4次分割。采用不良事件通用术语标准第4版(CTCAE v 4.0)对毒性进行分级。69例患者获得完全缓解(CR),6例部分缓解(PR),5例疾病稳定(SD)。疾病控制率(DCR = SD和ORR)和总缓解率(ORR = PR、CR或PR)分别为92.6%和85.2%。3年和5年估计总生存率(OS)分别为75.4%和66.3%,3年和5年估计无进展生存率(PFS)分别为78.2%和65.4%。PFS时间和OS时间的中位数分别为36.8个月和45.5个月。远处转移见于肺(3例)、盆腔壁(2例)、肝(3例)和骨(2例)。6例出现局部复发,2例患者出现局部复发并同时伴有全身转移性肿瘤。与过去的结果不同,吉西他滨和顺铂与适形放疗联合使用时似乎具有耐受性、有效性和可行性。

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