Louvel Guillaume, Metellus Philippe, Noel Georges, Peeters Sophie, Guyotat Jacques, Duntze Julien, Le Reste Pierre-Jean, Dam Hieu Phong, Faillot Thierry, Litre Fabien, Desse Nicolas, Petit Antoine, Emery Evelyne, Voirin Jimmy, Peltier Johann, Caire François, Vignes Jean-Rodolphe, Barat Jean-Luc, Langlois Olivier, Menei Philippe, Dumont Sarah N, Zanello Marc, Dezamis Edouard, Dhermain Frédéric, Pallud Johan
Department of Radiation Oncology, INSERM 1030 "Molecular Radiotherapy", Gustave Roussy, Gustave Roussy Cancer Campus, Villejuif, France.
Department of Neurosurgery, Clairval Private Hospital, Marseille, France; UMR911, CRO2, Aix-Marseille Université, France.
Radiother Oncol. 2016 Jan;118(1):9-15. doi: 10.1016/j.radonc.2016.01.001. Epub 2016 Jan 11.
To assess the influence of the time interval between surgical resection and standard combined chemoradiotherapy on survival in newly diagnosed and homogeneously treated (surgical resection plus standard combined chemoradiotherapy) glioblastoma patients; while controlling confounding factors (extent of resection, carmustine wafer implantation, functional status, neurological deficit, and postoperative complications).
From 2005 to 2011, 692 adult patients (434 men; mean of 57.5 ± 10.8 years) with a newly diagnosed glioblastoma were enrolled in this retrospective multicentric study. All patients were treated by surgical resection (65.5% total/subtotal resection, 34.5% partial resection; 36.7% carmustine wafer implantation) followed by standard combined chemoradiotherapy (radiotherapy at a median dose of 60 Gy, with daily concomitant and adjuvant temozolomide). Time interval to standard combined chemoradiotherapy was analyzed as a continuous variable and as a dichotomized variable using median and quartiles thresholds. Multivariate analyses using Cox modeling were conducted.
The median progression-free survival was 10.3 months (95% CI, 10.0-11.0). The median overall survival was 19.7 months (95% CI, 18.5-21.0). The median time to initiation of combined chemoradiotherapy was 1.5 months (25% quartile, 1.0; 75% quartile, 2.2; range, 0.1-9.0). On univariate and multivariate analyses, OS and PFS were not significantly influenced by time intervals to adjuvant treatments. On multivariate analysis, female gender, total/subtotal resection and RTOG-RPA classes 3 and 4 were significant independent predictors of improved OS.
Delaying standard combined chemoradiotherapy following surgical resection of newly diagnosed glioblastoma in adult patients does not impact survival.
评估手术切除与标准同步放化疗之间的时间间隔对新诊断且接受同质化治疗(手术切除加标准同步放化疗)的胶质母细胞瘤患者生存的影响;同时控制混杂因素(切除范围、卡莫司汀晶片植入、功能状态、神经功能缺损和术后并发症)。
2005年至2011年,692例新诊断为胶质母细胞瘤的成年患者(434例男性;平均年龄57.5±10.8岁)纳入这项回顾性多中心研究。所有患者均接受手术切除(65.5%全切除/次全切除,34.5%部分切除;36.7%卡莫司汀晶片植入),随后进行标准同步放化疗(放疗中位剂量60 Gy,每日同步及辅助替莫唑胺)。将至标准同步放化疗的时间间隔作为连续变量和使用中位数及四分位数阈值进行二分的变量进行分析。采用Cox模型进行多变量分析。
中位无进展生存期为10.3个月(95%CI,10.0 - 11.0)。中位总生存期为19.7个月(95%CI,18.5 - 21.0)。开始同步放化疗的中位时间为1.5个月(四分位数25%,1.0;四分位数75%,2.2;范围,0.1 - 9.0)。在单变量和多变量分析中,辅助治疗的时间间隔对总生存期和无进展生存期无显著影响。多变量分析显示,女性、全切除/次全切除以及RTOG - RPA 3级和4级是总生存期改善的显著独立预测因素。
成年患者新诊断的胶质母细胞瘤手术切除后延迟标准同步放化疗不影响生存。