Sastry Rahul A, Shankar Ganesh M, Gerstner Elizabeth R, Curry William T
Department of Surgery, Brigham & Women's Hospital, Harvard Medical School, 75 Francis Street - CA034, Boston, MA 02115, United States.
Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School, 55 Fruit Street, White 502, Boston, MA 02114, United States.
J Clin Neurosci. 2018 Jul;53:41-47. doi: 10.1016/j.jocn.2018.04.004. Epub 2018 Apr 19.
Despite updated management of glioblastoma (GB), progression is virtually inevitable. Previous data suggest a survival benefit from resection at progression; however, relatively few studies have evaluated the role of surgery in the context of contemporary GB treatment and widespread use of bevacizumab and chemotherapy. As such, the purpose of this study is to evaluate outcomes following surgical resection in patients with progressive GB since 2008. The records of all patients who underwent biopsy or resection of GB between January 1, 2008, and December 31, 2015, were retrospectively reviewed to identify 368 patients with progressive GB. Median survival and 95% confidence intervals were generated with the Kaplan-Meier method. Multivariate analysis, which controlled for age, Karnofsky Performance Status (KPS), extent of resection, adjuvant chemotherapy and radiation, tumor location, and tumor multifocality, of post-progression survival was carried out using a Cox proportional hazards model. Of 368 patients with progressive disease, 77 (20.9%) underwent resection at first documented progression. The median post-progression survivals for patients who did and did not undergo resection at this time were 12.8 and 7.0 months, respectively. In multivariate analysis, KPS ≥ 70 at progression (HR 0.438), receipt of bevacizumab at first progression (HR 0.756), and receipt of chemotherapy at first progression (HR 0.644) were associated with increased post-progression survival. Thus, surgery for progressive GB may not improve post-progression survival in the context of contemporary maximal non-surgical therapy. Further investigation is necessary to elucidate what role, if any, bevacizumab has in prolonging post-progression survival in patients with progressive GB.
尽管胶质母细胞瘤(GB)的治疗方法不断更新,但疾病进展几乎不可避免。既往数据表明,疾病进展时进行手术切除可带来生存获益;然而,相对较少的研究评估了手术在当代GB治疗以及贝伐单抗和化疗广泛应用背景下的作用。因此,本研究的目的是评估自2008年以来进展期GB患者手术切除后的预后。回顾性分析了2008年1月1日至2015年12月31日期间所有接受GB活检或切除的患者记录,以确定368例进展期GB患者。采用Kaplan-Meier法计算中位生存期和95%置信区间。使用Cox比例风险模型对进展后生存情况进行多因素分析,该分析控制了年龄、卡氏功能状态(KPS)、切除范围、辅助化疗和放疗、肿瘤位置以及肿瘤多灶性。在368例疾病进展的患者中,77例(20.9%)在首次记录到疾病进展时接受了手术切除。此时接受和未接受手术切除的患者进展后中位生存期分别为12.8个月和7.0个月。在多因素分析中,进展时KPS≥70(风险比[HR] 0.438)、首次进展时接受贝伐单抗治疗(HR 0.756)以及首次进展时接受化疗(HR 0.644)与进展后生存期延长相关。因此,在当代最大程度的非手术治疗背景下,进展期GB的手术治疗可能无法改善进展后生存期。有必要进一步研究以阐明贝伐单抗在延长进展期GB患者进展后生存期方面(如果有)所起的作用。