Dhall Girish, Grodman Howard, Ji Lingyun, Sands Stephen, Gardner Sharon, Dunkel Ira J, McCowage Geoffrey B, Diez Blanca, Allen Jeffrey C, Gopalan Anjali, Cornelius Albert S, Termuhlen Amanda, Abromowitch Minnie, Sposto Richard, Finlay Jonathan L
Childrens Hospital Los Angeles, Los Angeles, California, USA.
Pediatr Blood Cancer. 2008 Jun;50(6):1169-75. doi: 10.1002/pbc.21525.
To determine the survival of infants and young children with non-metastatic medulloblastoma using intensive myeloablative chemotherapy and autologous hematopoietic progenitor cell rescue (AuHCR).
Twenty-one children less than 3 years old at diagnosis with non-metastatic medulloblastoma were enrolled on two identical serial studies, "Head Start" I and "Head Start" II. After surgery, patients received five cycles of induction chemotherapy consisting of vincristine, cisplatin, cyclophosphamide and etoposide. Following induction, all patients underwent myeloablative chemotherapy using carboplatin, thiotepa and etoposide with AuHCR. Irradiation was used only at relapse.
The 5-year event-free (EFS) and overall survival (OS) rates (+/-SE) for all patients, patients with gross total resection, and patients with residual tumor were 52 +/- 11% and 70 +/- 10%, 64 +/- 13% and 79 +/- 11%, and 29 +/- 17% and 57 +/- 19%, respectively. The 5-year EFS and OS ( +/- SE) for patients with desmoplastic and classical medulloblastoma were 67 +/- 16% and 78 +/- 14%, and 42 +/- 14 and 67 +/- 14%, respectively. There were four treatment related deaths. The majority of survivors (71%) avoided irradiation completely. Mean intellectual functioning and quality of life (QoL) for children surviving without irradiation was within average range for a majority of survivors tested.
This strategy of brief intensive chemotherapy for young children with non-metastatic medulloblastoma eliminated the need for craniospinal irradiation 52% of the patients, and may preserve QoL and intellectual functioning. The excellent survival rates are somewhat dampened by high toxic mortality.
采用强化清髓性化疗和自体造血祖细胞挽救(AuHCR)来确定非转移性髓母细胞瘤婴幼儿的生存率。
21名诊断时年龄小于3岁的非转移性髓母细胞瘤患儿参加了两项相同的系列研究,即“抢先行动”I和“抢先行动”II。手术后,患者接受了由长春新碱、顺铂、环磷酰胺和依托泊苷组成的五个周期诱导化疗。诱导化疗后,所有患者使用卡铂、噻替派和依托泊苷并进行AuHCR进行清髓性化疗。仅在复发时使用放疗。
所有患者、全切患者和有残留肿瘤患者的5年无事件生存率(EFS)和总生存率(OS)(±SE)分别为52±11%和70±10%、64±13%和79±11%、29±17%和57±19%。促纤维增生型和经典型髓母细胞瘤患者的5年EFS和OS(±SE)分别为67±16%和78±14%、42±14%和67±14%。有4例治疗相关死亡。大多数幸存者(71%)完全避免了放疗。对于大多数接受测试的未接受放疗而存活的儿童,其平均智力功能和生活质量(QoL)在平均范围内。
这种针对非转移性髓母细胞瘤幼儿的短期强化化疗策略使52%的患者无需进行全脑全脊髓放疗,并可能保留QoL和智力功能。高毒性死亡率在一定程度上降低了出色的生存率。