Faculty of Advanced Techno-Surgery, Graduate School of Medicine, Tokyo Women's Medical University, Tokyo, Japan.
J Neurosurg. 2011 Aug;115(2):248-55. doi: 10.3171/2011.4.JNS10377. Epub 2011 May 13.
The objective of the present study was analysis of results of the prospective clinical trial directed toward the evaluation of therapeutic efficacy of the administration of autologous formalin-fixed tumor vaccine (AFTV) concomitant with fractionated radiotherapy in cases of newly diagnosed glioblastoma multiforme.
Twenty-four patients were enrolled into the clinical trial, while 2 cases were excluded from the final analysis of results. The treatment protocol included aggressive tumor resection, fractionated radiotherapy up to a total dose of 60 Gy, and 3 concomitant courses of AFTV administered with an interval of one week at the late stage of irradiation. Two delayed-type hypersensitivity (DTH) tests were done--one 48 hours before the initial course of vaccination (DTH-1) and one 2 weeks after the third (DTH-2). All but one of the patients received salvage therapy at the time of tumor progression. The defined primary end point was overall survival; secondary end points were progression-free survival and safety of concomitant treatment.
The median duration of overall survival was 19.8 [corrected] months (95% CI 13.8-31.3 months). The actuarial 2-year survival rate was 40%. The median duration of progression-free survival was 7.6 months (95% CI 4.3-13.6 months). Overall survival showed a statistically significant association with recursive partitioning analysis class (p < 0.05); progression-free survival showed a statistically significant association with p53 staining index (p < 0.05) and size of DTH-2 response (p < 0.001). AFTV injection concomitant with fractionated radiotherapy was well tolerated by all patients and in no case did treatment-related adverse effects exceed Grade 1 toxicity; adverse effects were limited to local erythema, induration, and swelling at the site of injection.
The results of this study demonstrate that AFTV treatment concomitant with fractionated radiotherapy may be effective in patients with newly diagnosed glioblastoma. Further clinical testing is warranted.
本研究的目的是分析一项前瞻性临床试验的结果,该试验旨在评估在新诊断的多形性胶质母细胞瘤患者中,同时给予自体福尔马林固定肿瘤疫苗(AFTV)和分割放疗的治疗效果。
24 名患者入组该临床试验,其中 2 例被排除在最终结果分析之外。治疗方案包括积极的肿瘤切除术、分割放疗至总剂量 60Gy,以及在放疗后期的第 3 个疗程同时给予 3 个 AFTV 疗程,间隔 1 周。进行了 2 次迟发型超敏反应(DTH)测试——1 次在初始疫苗接种前 48 小时(DTH-1),1 次在第 3 次后 2 周(DTH-2)。除 1 例患者外,所有患者在肿瘤进展时均接受了挽救治疗。定义的主要终点是总生存期;次要终点是无进展生存期和联合治疗的安全性。
总生存期的中位数为 19.8 个月(95%CI 13.8-31.3 个月)。2 年生存率的估计值为 40%。无进展生存期的中位数为 7.6 个月(95%CI 4.3-13.6 个月)。总生存期与递归分区分析类别显著相关(p<0.05);无进展生存期与 p53 染色指数显著相关(p<0.05),与 DTH-2 反应大小显著相关(p<0.001)。所有患者均能耐受 AFTV 注射与分割放疗联合治疗,且无治疗相关不良反应超过 1 级毒性;不良反应仅限于注射部位的局部红斑、硬结和肿胀。
本研究结果表明,AFTV 治疗与分割放疗联合应用可能对新诊断的胶质母细胞瘤患者有效。需要进一步的临床测试。