Shrieve D C, Wara W M, Edwards M S, Sneed P K, Prados M D, Cogen P H, Larson D A, Levin V A
Dept. of Radiation Oncology, University of California, School of Medicine, San Francisco 94143-0226.
Int J Radiat Oncol Biol Phys. 1992;24(4):599-610. doi: 10.1016/0360-3016(92)90704-l.
Between February 1984 and September 1990, 60 patients with brainstem gliomas were treated with hyperfractionated radiotherapy in the Department of Radiation Oncology at the University of California, San Francisco. Forty-one children (< or = 18 years) and 19 adults were treated with 100 cGy twice daily with 4-8 hr between doses. Thirty-one patients (21 children and 10 adults) received total doses of 66-72 Gy and 29 patients (20 children and nine adults) received 74-78 Gy. Median follow-up was 208 weeks for all patients (214 weeks for children, 157 weeks for adults). Twenty-three patients (14 children and nine adults) were alive at the time of analysis, surviving 59-359 weeks following treatment. Median actuarial survival was 73.6 weeks overall (72 weeks for children, 190 weeks for adults; p = 0.43). Survival at 12 and 24 months was 65% and 38%, respectively (63% and 32%, for children; 68% and 53% for adults). All patients had pretreatment magnetic resonance imaging by which tumors were classified as either focal or diffuse. No significant pretreatment prognostic factors for adults were identified. In children, significant favorable prognostic factors on univariate analysis were older age (p = 0.001), tumor location in thalamus or midbrain (p = 0.002), focal appearance on MRI scan (p < 0.001) and duration of symptoms > 2 months prior to treatment (p < 0.001). Thirty-five patients had tumor biopsies, leading to a diagnosis in 33 (22 children and 11 adults). Children with moderately anaplastic astrocytomas survived significantly longer than those with glioblastoma multiforme or unbiopsied tumors (p < 0.001). Only duration of symptoms > 2 months remained significant as a favorable prognostic indicator for children on multivariate analysis (p < 0.001). Survival was not significantly different for patients receiving < or = 72 Gy and those receiving > 72 Gy (p = 0.18). No subgroup of patients showed significantly better survival with the higher dose. These findings indicate that hyperfractionated radiotherapy is effective treatment for adults and a subgroup of better prognosis children with brainstem gliomas. There is a subgroup of pediatric patients with extremely poor prognosis for whom even this aggressive treatment does little to extend survival. We conclude that there is no benefit to increasing total dose above 72 Gy for any of the groups analyzed.
1984年2月至1990年9月期间,加利福尼亚大学旧金山分校放射肿瘤学系对60例脑干胶质瘤患者进行了超分割放射治疗。41名儿童(≤18岁)和19名成人接受了每日两次、每次100 cGy的治疗,两次剂量之间间隔4 - 8小时。31例患者(21名儿童和10名成人)接受的总剂量为66 - 72 Gy,29例患者(20名儿童和9名成人)接受的总剂量为74 - 78 Gy。所有患者的中位随访时间为208周(儿童为214周,成人为157周)。分析时,23例患者(14名儿童和9名成人)存活,治疗后存活59 - 359周。总体中位精算生存期为73.6周(儿童为72周,成人为190周;p = 0.43)。12个月和24个月时的生存率分别为65%和38%(儿童为63%和32%;成人为68%和53%)。所有患者在治疗前均进行了磁共振成像检查,据此将肿瘤分为局灶性或弥漫性。未发现成人患者治疗前有显著的预后因素。在儿童中,单因素分析显示显著的有利预后因素为年龄较大(p = 0.001)、肿瘤位于丘脑或中脑(p = 0.002)、MRI扫描表现为局灶性(p < 0.001)以及治疗前症状持续时间>2个月(p < 0.001)。35例患者进行了肿瘤活检,33例(22名儿童和11名成人)得以确诊。中度间变性星形细胞瘤患儿的生存期明显长于多形性胶质母细胞瘤患儿或未活检肿瘤患儿(p < 0.001)。多因素分析显示,仅症状持续时间>2个月仍是儿童患者有利的预后指标(p < 0.001)。接受≤72 Gy和>72 Gy的患者生存率无显著差异(p = 0.18)。没有亚组患者接受更高剂量时生存率有显著改善。这些结果表明,超分割放射治疗对成人和一部分预后较好的脑干胶质瘤患儿是有效的治疗方法。有一小部分儿科患者预后极差,即使采用这种积极的治疗方法,对延长生存期作用也不大。我们得出结论,对于所分析的任何组,将总剂量增加到72 Gy以上均无益处。