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Clinical efficacy and toxicity of radio-chemotherapy and magnetic resonance imaging-guided brachytherapy for locally advanced cervical cancer patients: A mono-institutional experience

机译:放射化学疗法和磁共振成像引导的近距离放射疗法对局部晚期宫颈癌患者的临床疗效和毒性:单机构经验

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Background. To evaluate efficacy and toxicity of radio-chemotherapy (RCT) and MR-guided pulsed-dose-rate (PDR) adaptive brachytherapy (IGABT) for locally advanced cervical cancer (LACC).Material and methods. Between 2007 and 2014 85 patients with FIGO stage 1B1 N+ or 1B2 cervical cancer were treated with RCT+ IGABT. The treatment consisted of a pelvic paraaortic external beam radiotherapy (EBRT) (45-50.4 Gy 10 Gy boost to primary tumor and/or to pathologic lymph nodes) with concurrent cisplatin followed by 25-35 Gy of PDR IGABT in 30-50 pulses. The ratio of 3D-CFRT/IMRT was 61/24 patients. Dose-volume parameters of high-risk clinical target volume (HR-CTV), intermediate-risk clinical target volume (IR-CTV) and D2cm(3) organs at risk (OARs) were reported. Local control (LC), cancer-specific survival (CCS) and overall survival (OS) were analyzed actuarially and morbidity crude rates were scored using CTCAEv4.0.Results. Mean follow-up was 36 months (range 6-94). The mean D90 and D98 for HR-CTV was 84.4 +/- 9 Gy and 77 +/- 8.1 Gy, while for IR-CTV was 69.1 +/- 4.3 Gy and 64.8 +/- 4.3 Gy, respectively. The mean D2cm(3) for OARs was the following: bladder: 77.3 +/- 10.5 Gy, rectum: 65 +/- 6.8 Gy, sigmoid: 63 +/- 7.9 Gy and intestine: 64.0 +/- 9.1 Gy. Three year LC, CSS and OS were: 94%, 85% and 81%. The three-year regional- and distant control rates were 95% and 74%. Node negative patients had significantly higher three-year CSS (100 vs. 72%, p = 0.016) and OS (92 vs. 72%, p = 0.001) compared to node positive ones. Three-year actuarial late Grade 3 morbidity was the following: GI: 8%, GU: 5%, Vaginal: 8%. The frequency of Grade 3 hematological toxicities including anemia/leukopeniaeutropenia/thrombocytopenia were 8.6%/34.7%/24.3%/24.3%, respectively.Conclusion. This large mono-institutional experience builds up further evidences that IGABT in conjunction with RCT should be the standard of care for patients suffering LACC.
机译:背景。评估放射化学疗法(RCT)和MR引导的脉冲剂量率(PDR)自适应近距离放射疗法(IGABT)对局部晚期宫颈癌(LACC)的疗效和毒性。材料和方法。在2007年至2014年之间,使用RCT + IGABT治疗了85例FIGO期1B1 N +或1B2宫颈癌患者。该治疗由盆腔主动脉外束放射疗法(EBRT)(对原发肿瘤和/或病理淋巴结有45-50.4 Gy的10 Gy增强作用)与顺铂同时进行,然后在30-50脉冲中进行25-35 Gy的PDR IGABT。 3D-CFRT / IMRT的比例为61/24患者。报告了高危临床目标体积(HR-CTV),中危临床目标体积(IR-CTV)和处于危险中的D2cm(3)器官(OAR)的剂量体积参数。精算分析局部对照(LC),癌症特异性存活率(CCS)和总体存活率(OS),并使用CTCAEv4.0对发病率粗率进行评分。平均随访36个月(范围6-94)。 HR-CTV的平均D90和D98为84.4 +/- 9 Gy和77 +/- 8.1 Gy,而IR-CTV的平均D90为69.1 +/- 4.3 Gy和64.8 +/- 4.3 Gy。 OAR的平均D2cm(3)如下:膀胱:77.3 +/- 10.5 Gy,直肠:65 +/- 6.8 Gy,乙状结肠:63 +/- 7.9 Gy,肠:64.0 +/- 9.1 Gy。三年的LC,CSS和OS分别为:94%,85%和81%。三年区域和远程控制率分别为95%和74%。与淋巴结阳性患者相比,淋巴结阴性患者的三年期CSS(100 vs. 72%,p = 0.016)和OS(92 vs. 72%,p = 0.001)明显更高。三年精算晚期3级发病率是:GI:8%,GU:5%,阴道:8%。包括贫血/白血球减少/中性粒细胞减少/血小板减少在内的3级血液学毒性发生率分别为8.6%/ 34.7%/ 24.3%/ 24.3%。这种庞大的单一机构经验进一步证明了IGABT与RCT结合应成为患有LACC的患者的治疗标准。

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