Department of Pediatric Oncology, University Children's Hospital, Zurich, Switzerland.
Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Int J Radiat Oncol Biol Phys. 2014 Jul 15;89(4):863-71. doi: 10.1016/j.ijrobp.2014.04.017.
The prognosis for children with central nervous system primitive neuroectodermal tumor (CNS-PNET) or pinealoblastoma is still unsatisfactory. Here we report the results of patients between 4 and 21 years of age with nonmetastatic CNS-PNET or pinealoblastoma diagnosed from January 2001 to December 2005 and treated in the prospective GPOH-trial P-HIT 2000-AB4.
After surgery, children received hyperfractionated radiation therapy (36 Gy to the craniospinal axis, 68 Gy to the tumor region, and 72 Gy to any residual tumor, fractionated at 2 × 1 Gy per day 5 days per week) accompanied by weekly intravenous administration of vincristine and followed by 8 cycles of maintenance chemotherapy (lomustine, cisplatin, and vincristine).
Twenty-six patients (15 with CNS-PNET; 11 with pinealoblastoma) were included. Median age at diagnosis was 11.5 years old (range, 4.0-20.7 years). Gross total tumor resection was achieved in 6 and partial resection in 16 patients (indistinct, 4 patients). Median follow-up of the 15 surviving patients was 7.0 years (range, 5.2-10.0 years). The combined response rate to postoperative therapy was 17 of 20 (85%). Eleven of 26 patients (42%; 7 of 15 with CNS-PNET; 4 of 11 with pinealoblastoma) showed tumor progression or relapse at a median time of 1.3 years (range, 0.5-1.9 years). Five-year progression-free and overall survival rates (± standard error [SE]) were each 58% (± 10%) for the entire cohort: CNS-PNET was 53% (± 13); pinealoblastoma was 64% (± 15%; P=.524 and P=.627, respectively).
Postoperative hyperfractionated radiation therapy with local dose escalation followed by maintenance chemotherapy was feasible without major acute toxicity. Survival rates are comparable to those of a few other recent studies but superior to those of most other series, including the previous trial, HIT 1991.
儿童中枢神经系统原始神经外胚层肿瘤(CNS-PNET)或松果体母细胞瘤的预后仍然不理想。在这里,我们报告了 2001 年 1 月至 2005 年 12 月期间在前瞻性 GPOH-trial P-HIT 2000-AB4 中诊断为非转移性 CNS-PNET 或松果体母细胞瘤且接受治疗的 4 至 21 岁患者的结果。
手术后,患儿接受超分割放射治疗(颅脊柱轴 36Gy,肿瘤区域 68Gy,任何残留肿瘤 72Gy,每天 2 次,每次 1Gy,每周 5 天),同时每周静脉注射长春新碱,随后进行 8 个周期的维持化疗(洛莫司汀、顺铂和长春新碱)。
26 例患者(15 例 CNS-PNET;11 例松果体母细胞瘤)入选。中位诊断年龄为 11.5 岁(范围,4.0-20.7 岁)。6 例患者行肿瘤全切除,16 例患者行部分切除(4 例不明确)。15 例存活患者的中位随访时间为 7.0 年(范围,5.2-10.0 年)。术后治疗的综合反应率为 20 例中的 17 例(85%)。26 例患者中有 11 例(42%;15 例 CNS-PNET 中有 7 例;11 例松果体母细胞瘤中有 4 例)在中位时间 1.3 年内(范围,0.5-1.9 年)出现肿瘤进展或复发。全队列的 5 年无进展生存率和总生存率(±标准误差[SE])分别为 58%(±10%):CNS-PNET 为 53%(±13%);松果体母细胞瘤为 64%(±15%;P=.524 和 P=.627)。
局部剂量递增的术后超分割放疗联合维持化疗没有出现严重的急性毒性,是可行的。生存率与少数其他近期研究相当,但优于大多数其他系列,包括之前的 HIT 1991 试验。