Frappaz Didier, Schell Matthias, Thiesse Philippe, Marec-Bérard Perrine, Mottolese Carmine, Perol David, Bergeron Christophe, Philip Thierry, Ricci Anne Claire, Galand-Desme Sophie, Szathmari Alexandru, Carrie Christian
Pediatric Department, Centre Léon Bérard, Lyon, France.
Neuro Oncol. 2008 Aug;10(4):599-607. doi: 10.1215/15228517-2008-029. Epub 2008 Jun 24.
Radiation therapy remains the only treatment that provides clinical benefit to children with diffuse brainstem tumors. Their median survival, however, rarely exceeds 9 months. The authors report a prospective trial of frontline chemotherapy aimed at delaying radiation until time of clinical progression. The aim was to investigate the possibility that radiotherapy would maintain its activity in children whose disease progressed after chemotherapy. Twenty-three patients took part in this protocol, the BSG 98 protocol, which consisted of frontline chemotherapy alternating hematotoxic and nonhematotoxic schedules. Each cycle included three courses delivered monthly; the first course was 1,3-bis(2-chloroethyl)-1-nitrosoureacisplatin, and the second and third were high-dose methotrexate. Three patients underwent one cycle; 5 patients each, two and three cycles; and 10 patients, four cycles. Twenty of the 23 patients eventually received local radiation therapy. A historical cohort of 14 patients who received at least local radiation therapy served as controls. Four patients experienced severe iatrogenic infections, and 11 patients required platelet transfusions. Median survival increased significantly in patients participating in the protocol compared to that in the historical controls (17 months, 95% confidence interval [CI], 10-23 months, vs. 9 months, 95% CI, 8-10 months; p = 0.022), though hospitalization was prolonged (57 vs. 25 days, p = 0.001). Although frontline chemotherapy alternating hematotoxic and nonhematotoxic schedules significantly increases overall median survival, its cost from infection and hospitalization deserves honest discussion with the children and their parents.
放射治疗仍然是唯一能给患有弥漫性脑干肿瘤的儿童带来临床益处的治疗方法。然而,他们的中位生存期很少超过9个月。作者报告了一项一线化疗的前瞻性试验,旨在将放疗推迟到临床进展时。目的是研究在化疗后疾病进展的儿童中,放疗是否仍能保持其有效性。23名患者参与了该方案,即BSG 98方案,该方案由交替使用血液毒性和非血液毒性方案的一线化疗组成。每个周期包括每月进行的三个疗程;第一个疗程是1,3-双(2-氯乙基)-1-亚硝基脲和顺铂,第二个和第三个疗程是高剂量甲氨蝶呤。3名患者接受了一个周期的治疗;5名患者各接受了两个和三个周期的治疗;10名患者接受了四个周期的治疗。23名患者中有20名最终接受了局部放射治疗。14名至少接受了局部放射治疗的患者组成的历史队列作为对照。4名患者发生了严重的医源性感染,11名患者需要输注血小板。与历史对照组相比,参与该方案的患者中位生存期显著延长(17个月,95%置信区间[CI],10 - 23个月,而历史对照组为9个月,95%CI,8 - 10个月;p = 0.022),尽管住院时间延长了(57天对25天,p = 0.001)。虽然交替使用血液毒性和非血液毒性方案的一线化疗显著提高了总体中位生存期,但其因感染和住院产生的费用值得与儿童及其家长进行坦诚的讨论。