Van Damme Axel, Tummers Philippe, De Visschere Pieter, Van Dorpe Jo, Van de Vijver Koen, Vercauteren Tom, De Gersem Werner, Denys Hannelore, Naert Eline, Makar Amin, De Neve Wilfried, Vandecasteele Katrien
Department of Radiation Oncology, Ghent University Hospital, Ghent, Belgium.
Department of Gynaecology, Ghent University Hospital, Ghent, Belgium.
Clin Transl Radiat Oncol. 2024 May 11;47:100793. doi: 10.1016/j.ctro.2024.100793. eCollection 2024 Jul.
Chemoradiotherapy followed by brachytherapy is the standard of care for locally advanced cervical cancer (LACC). In this study, we postulate that omitting an iconographical unaffected uterus (+12 mm distance from the tumour) from the treatment volume is safe and that no tumour will be found in the non-targeted uterus (NTU) leading to reduction of high-dose volumes of surrounding organs at risk (OARs).
In this single-arm phase 2 study, two sets of target volumes were delineated: one standard-volume (whole uterus) and an EXIT-volume (exclusion of non-tumour-bearing parts of the uterus with a minimum 12 mm margin from the tumour). All patients underwent chemoradiotherapy targeting the EXIT-volume, followed by completion hysterectomy. In 15 patients, a plan comparison between two treatment plans (PTV vs PTV_EXIT) was performed. The primary endpoint was the pathological absence of tumour involvement in the non-targeted uterus (NTU). Secondary endpoints included dosimetric impact of target volume reduction on OARs, acute and chronic toxicity, overall survival (OS), locoregional recurrence-free survival (LRFS), and progression-free survival (PFS).
In all 21 (FIGO stage I: 2; II: 14;III: 3; IV: 2) patients the NTU was pathologically negative. Ssignificant reductions in Dmean in bladder, sigmoid and rectum; V15Gy in sigmoid and rectum, V30Gy in bladder, sigmoid and rectum; V40Gy and V45Gy in bladder, bowel bag, sigmoid and rectum; V50Gy in rectum were achieved. Median follow-up was 54 months (range 7-79 months). Acute toxicity was mainly grade 2 and 5 % grade 3 urinary. The 3y- OS, PFS and LRFS were respectively 76,2%, 64,9% and 81 %.
MRI-based exclusion of the non-tumour-bearing parts of the uterus at a minimum distance of 12 mm from the tumour out of the target volume in LACC can be done without risk of residual disease in the NTU, leading to a significant reduction of the volume of surrounding OARS treated to high doses.
同步放化疗后行近距离放疗是局部晚期宫颈癌(LACC)的标准治疗方案。在本研究中,我们推测从治疗靶区中排除影像学上未受影响的子宫(距肿瘤12毫米以外)是安全的,且在非靶区子宫(NTU)中不会发现肿瘤,从而减少周围危及器官(OARs)的高剂量照射体积。
在这项单臂2期研究中,划定了两组靶区:一个标准靶区(全子宫)和一个EXIT靶区(排除子宫非肿瘤部分,距肿瘤边缘至少12毫米)。所有患者均接受针对EXIT靶区的同步放化疗,随后行子宫全切术。对15例患者进行了两种治疗计划(PTV与PTV_EXIT)的计划比较。主要终点是病理检查显示非靶区子宫(NTU)无肿瘤累及。次要终点包括靶区体积缩小对OARs的剂量学影响、急性和慢性毒性、总生存期(OS)、局部区域无复发生存期(LRFS)和无进展生存期(PFS)。
在所有21例患者(国际妇产科联盟分期:I期2例;II期14例;III期3例;IV期2例)中,NTU病理检查均为阴性。膀胱、乙状结肠和直肠的平均剂量(Dmean)显著降低;乙状结肠和直肠的V15Gy、膀胱、乙状结肠和直肠的V30Gy、膀胱、肠袋、乙状结肠和直肠的V40Gy和V4·5Gy、直肠的V50Gy均显著降低。中位随访时间为54个月(范围7 - 79个月)。急性毒性主要为2级,5%为3级泌尿系统毒性。3年总生存期、无进展生存期和局部区域无复发生存期分别为76.2%、64.9%和81%。
在LACC中,基于MRI将距肿瘤至少12毫米的子宫非肿瘤部分排除在靶区之外,不会有NTU残留疾病的风险,从而显著减少接受高剂量照射的周围OARs的体积。