Deakin University, Geelong, Australia.
J Clin Oncol. 2012 Sep 10;30(26):3181-6. doi: 10.1200/JCO.2010.34.4341. Epub 2012 Jul 30.
P9934 was a prospective trial of systemic chemotherapy, second surgery, and conformal radiation therapy (CRT) limited to the posterior fossa and primary site for children between 8 months and 3 years old with nonmetastatic medulloblastoma. The study was open from June 2000 until June 2006.
After initial surgery, children received four cycles of induction chemotherapy, followed by age- and response-adjusted CRT to the posterior fossa (18 or 23.4 Gy) and tumor bed (cumulative 50.4 or 54 Gy) and maintenance chemotherapy. Neurodevelopmental outcomes were evaluated and event-free survival (EFS) results were directly compared with a previous study of multiagent chemotherapy without irradiation (Pediatric Oncology Group [POG] trial 9233).
Seventy-four patients met eligibility requirements. The 4-year EFS and overall survival probabilities were 50% ± 6% and 69% ± 5.5%, respectively, which compared favorably to the results from POG 9233. Analysis showed that the desmoplastic/nodular subtype was a favorable factor in predicting survival. Our 4-year EFS rate was 58% ± 8% for patients with desmoplasia. Whereas seven of 10 patients who had disease progression before CRT had primary-site failure, 15 of 19 patients who progressed after CRT had distant-site failure. Neurodevelopmental assessments did not show a decline in cognitive or motor function after protocol-directed chemotherapy and CRT.
The addition of CRT to postoperative chemotherapy in young children with nonmetastatic medulloblastoma increased event-free survival compared with the use of postoperative chemotherapy alone. Future studies will use histopathologic typing (desmoplastic/nodular versus nondesmoplastic/nodular) to stratify patients for therapy by risk of relapse.
P9934 是一项前瞻性临床试验,研究对象为 8 个月至 3 岁的非转移性髓母细胞瘤患儿,他们接受全身化疗、二次手术以及局限于后颅窝和原发部位的适形放疗(CRT)。该研究于 2000 年 6 月至 2006 年 6 月开放入组。
初始手术后,患儿接受 4 个周期的诱导化疗,随后根据年龄和反应调整 CRT 剂量,照射后颅窝(18 或 23.4 Gy)和肿瘤床(累积 50.4 或 54 Gy),并进行维持化疗。评估神经发育结局,并直接比较本研究与既往未放疗的多药化疗(儿科肿瘤组 [POG] 试验 9233)的无事件生存(EFS)结果。
74 例患儿符合入组条件。4 年 EFS 和总生存率分别为 50%±6%和 69%±5.5%,优于 POG 9233 研究结果。分析显示,促纤维增生/结节型是预测生存的有利因素。我们的研究中,促纤维增生型患儿 4 年 EFS 率为 58%±8%。10 例 CRT 前疾病进展的患儿中有 7 例原发部位失败,19 例 CRT 后疾病进展的患儿中有 15 例出现远处转移失败。基于方案的化疗和 CRT 后神经发育评估未显示认知或运动功能下降。
与单纯术后化疗相比,年轻非转移性髓母细胞瘤患儿术后化疗联合 CRT 可提高 EFS。未来的研究将使用组织病理学类型(促纤维增生/结节型与非促纤维增生/结节型)对患者进行分层,以确定复发风险分层的治疗策略。