Gnekow A K, Kaatsch P, Kortmann R, Wiestler O D
Klinik für Kinder und Jugendliche, KZV Augsburg.
Klin Padiatr. 2000 Jul-Aug;212(4):177-84. doi: 10.1055/s-2000-9674.
The rationale of the HIT-LGG protocol is to delay standard radiotherapy through administration of chemotherapy for children with progressive low grade glioma at an age under 5 years and in older children upon individual decision.
Until October 10th., 1999, 402 patients from 69 hospitals were registered. 130 children with progressive tumors were treated after a median observation time of 5 months: 46 patients received primary radiotherapy and 84 primary chemotherapy. A ten week induction period with weekly Vincristine and pulses of Carboplatin at weeks 1, 4, 7 and 10 is followed by consolidation with simultaneous application of both drugs every 4 weeks until week 53.
Of 84 patients in the chemotherapy arm of the study (49 male, 35 female, 23 NF I, median age 2.99 years) 36 received treatment at diagnosis and 43 after a median observation time of 19.7 months. 94.3% achieved a clinical and neuroradiological response according to protocol criteria (5 CR, 30 PR/OR, 31 SD) after a median of 5.1 months. 4 tumors showed primary progression (9 too early, 5 not known). Only 6 of 84 children received radiation therapy for progressive disease during (2) or after termination (4) of chemotherapy, after a median delay of 25.6 months at a median age of 6.0 years. At a median observation time of 21.0 months, 6 children are in CR, 11 in PR, 48 have SD, 4 tumors are progressive and 3 children died of their tumor. (9 too early, 3 not known). PFS is at 72% after 36 months. 24 of 27 children experiencing allergic reactions to Carboplatin had to interrupt chemotherapy prematurely.
Combination therapy with Carboplatin and Vincristine can effectively delay the start of radiotherapy in children with progressive low-grade glioma. The high rate of hypersensitivity reactions has to prompt future modifications of treatment.
HIT-LGG方案的基本原理是,对于5岁以下进展性低级别胶质瘤儿童以及年龄较大儿童(根据个体情况决定),通过给予化疗来延迟标准放疗。
截至1999年10月10日,来自69家医院的402例患者进行了登记。130例肿瘤进展的儿童在中位观察时间5个月后接受了治疗:46例患者接受了初始放疗,84例接受了初始化疗。先进行为期10周的诱导期,每周使用长春新碱,并在第1、4、7和10周给予卡铂脉冲治疗,随后每4周同时应用两种药物进行巩固治疗,直至第53周。
在研究的化疗组84例患者中(49例男性,35例女性,23例患有神经纤维瘤病I型,中位年龄2.99岁),36例在诊断时接受治疗,43例在中位观察时间19.7个月后接受治疗。中位5.1个月后,94.3%的患者根据方案标准达到临床和神经放射学缓解(5例完全缓解,30例部分缓解/客观缓解,31例疾病稳定)。4例肿瘤出现原发进展(9例过早进展,5例情况不明)。84例儿童中只有6例在化疗期间(2例)或化疗结束后(4例)因疾病进展接受了放射治疗,中位延迟25.6个月,中位年龄6.0岁。中位观察时间21.0个月时,6例儿童完全缓解,11例部分缓解,48例疾病稳定,4例肿瘤进展,3例儿童死于肿瘤(9例过早死亡,3例情况不明)。36个月时无进展生存期为72%。27例对卡铂过敏的儿童中有24例不得不提前中断化疗。
卡铂和长春新碱联合治疗可有效延迟进展性低级别胶质瘤儿童放疗的开始时间。高敏反应发生率高促使未来对治疗方案进行调整。