Gross M W, Altscher R, Brandtner M, Häusser-Mischlich H, Kiricuta I C, Siegmann A D, Engenhart-Cabillic R
Department of Radiotherapy and Radiooncology, Philipps-University of Marburg, Germany.
Strahlenther Onkol. 2001 Dec;177(12):656-61. doi: 10.1007/pl00002380.
Because of the pronounced radioresistance of glioblastoma multiforme the prognosis of this disease remains poor. Therefore, we investigated the impact of an additional simultaneous chemotherapy with the topoisomerase-I inhibitor topotecan (Hycamtin) on the quality of life and toxicity of radiotherapy.
In this multicenter trial patients with histologically proven glioblastoma multiforme underwent a simultaneous radio-chemotherapy. Including pilot phase 60 patients, 41 male and 19 female, were treated. Age ranged from 26 to 76 years, the mean was 57 years. Conventional fractionated conformal radiotherapy was performed with daily doses of 2.0 Gy to a total dose of 60 Gy. 1 hour prior to irradiation 0.5 mg (absolute dose) of topotecan were administered intravenously resulting in a cumulative dose of 15 mg. Besides hematologic and non-hematologic toxicity, quality of life was assessed by Karnofsky index and Spitzer index. Additionally local control and survival time were recorded.
57 patients completed the combined therapy. Median administered dose of radiation was 60 Gy (16-76 Gy). Median cumulative topotecan dose was 15 mg (7.5-18.5 mg). Grade-III toxicity was found in six cases (two hematologic, two motoric disorder, one infection, one nausea) and grade-IV toxicity in three cases (one esophagitis, one motoric disorder, one mental disorder). Two patients died of septic disease most likely caused by steroid induced immunosuppression. Mean Karnofsky index and Spitzer index initially, at the end of therapy and 6 weeks after therapy showed values of 87%, 81% and 80% and 19 points, 18 points and 19 points, respectively. Median survival time was 15 months.
This multimodal approach for patients with glioblastoma multiforme is well tolerated. Quality of life remains preserved and outpatient treatment is possible. The relatively long median survival time even for patients bearing macroscopic tumors is promising.
由于多形性胶质母细胞瘤具有明显的放射抗性,该疾病的预后仍然很差。因此,我们研究了拓扑异构酶-I抑制剂拓扑替康(希美康)同步化疗对放疗生活质量和毒性的影响。
在这项多中心试验中,组织学确诊为多形性胶质母细胞瘤的患者接受同步放化疗。包括试点阶段在内,共治疗了60例患者,其中男性41例,女性19例。年龄范围为26至76岁,平均年龄为57岁。采用常规分割适形放疗,每日剂量为2.0 Gy,总剂量为60 Gy。在放疗前1小时静脉注射0.5 mg(绝对剂量)拓扑替康,累积剂量为15 mg。除血液学和非血液学毒性外,通过卡诺夫斯基指数和斯皮策指数评估生活质量。此外,记录局部控制情况和生存时间。
57例患者完成了联合治疗。放疗的中位给药剂量为60 Gy(16 - 76 Gy)。拓扑替康的中位累积剂量为15 mg(7.5 - 18.5 mg)。6例出现III级毒性(2例血液学毒性、2例运动障碍、1例感染、1例恶心),3例出现IV级毒性(1例食管炎、1例运动障碍、1例精神障碍)。2例患者死于败血症,很可能是由类固醇诱导的免疫抑制引起的。治疗开始时、治疗结束时和治疗后6周的平均卡诺夫斯基指数和斯皮策指数分别为87%、81%和80%以及19分、18分和19分。中位生存时间为15个月。
这种针对多形性胶质母细胞瘤患者的多模式方法耐受性良好。生活质量得以维持,门诊治疗可行。即使对于有肉眼可见肿瘤的患者,相对较长的中位生存时间也很有前景。