Mason W P, Grovas A, Halpern S, Dunkel I J, Garvin J, Heller G, Rosenblum M, Gardner S, Lyden D, Sands S, Puccetti D, Lindsley K, Merchant T E, O'Malley B, Bayer L, Petriccione M M, Allen J, Finlay J L
Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
J Clin Oncol. 1998 Jan;16(1):210-21. doi: 10.1200/JCO.1998.16.1.210.
To evaluate a strategy that avoids radiotherapy in children less than 6 years of age with newly diagnosed malignant brain tumors, by administering myeloablative consolidation chemotherapy with autologous bone marrow reconstitution (ABMR) after maximal surgical resection and conventional induction chemotherapy.
Between March 1991 and April 1995, 62 children (median age, 30 months) with newly diagnosed malignant brain tumors were enrolled onto this trial. Children received conventional induction chemotherapy with vincristine, cisplatin, cyclophosphamide, and etoposide, repeated every 3 weeks for five cycles. Children without disease progression on induction chemotherapy were offered consolidation with myeloablative chemotherapy that incorporated carboplatin, thiotepa, and etoposide followed by ABMR. Irradiation was used only for residual tumor at consolidation or for progressive/recurrent disease.
Induction chemotherapy was well tolerated by most patients; however, progression was noted in 17 children (27%) and four (6%) died of treatment complications. Of 37 children who received consolidation chemotherapy with ABMR, 15 are free of disease progression (median post-ABMR without further treatment, >44 months). The remaining 22 all progressed within 15 months of ABMR; three of 37 (8%) died of treatment-related complications. The 3-year overall survival (OS) and event-free survival (EFS) rates from diagnosis for all children are 40% (95% confidence interval [CI], 28% to 52%) and 25% (95% CI, 13% to 37%), respectively. Radiotherapy was administered to 19 of 62 children: 17 for progressive disease (PD) and two for residual disease at the time of ABMR.
A significant proportion of children with malignant brain tumors can avoid radiotherapy and prolonged maintenance chemotherapy yet still achieve durable remission with this brief intensive chemotherapy regimen.
通过在最大程度手术切除和传统诱导化疗后给予清髓性巩固化疗及自体骨髓重建(ABMR),评估一种避免对新诊断的恶性脑肿瘤6岁以下儿童进行放疗的策略。
1991年3月至1995年4月期间,62名新诊断为恶性脑肿瘤的儿童(中位年龄30个月)被纳入该试验。儿童接受长春新碱、顺铂、环磷酰胺和依托泊苷的传统诱导化疗,每3周重复一次,共五个周期。诱导化疗无疾病进展的儿童接受含卡铂、噻替派和依托泊苷的清髓性化疗巩固治疗,随后进行ABMR。放疗仅用于巩固治疗时的残留肿瘤或疾病进展/复发情况。
大多数患者对诱导化疗耐受性良好;然而,17名儿童(27%)出现疾病进展,4名(6%)死于治疗并发症。在37名接受ABMR巩固化疗的儿童中,15名无疾病进展(ABMR后中位无进一步治疗时间>44个月)。其余22名在ABMR后15个月内均出现进展;37名中有3名(8%)死于治疗相关并发症。所有儿童从诊断起的3年总生存率(OS)和无事件生存率(EFS)分别为40%(95%置信区间[CI],28%至52%)和25%(95%CI,13%至37%)。62名儿童中有19名接受了放疗:17名因疾病进展(PD),2名因ABMR时的残留疾病。
相当一部分恶性脑肿瘤儿童可以避免放疗和长期维持化疗,但通过这种简短的强化化疗方案仍能实现持久缓解。