Department of Neurology, University Hospital Odense and Clinical Institute, University of Southern Denmark, Odense, Denmark.
Department of Neurology, University of Regensburg, Regensburg, Germany.
Neuro Oncol. 2018 Feb 19;20(3):400-410. doi: 10.1093/neuonc/nox155.
Medulloblastoma in adult patients is rare, with 0.6 cases per million. Prognosis depends on clinical factors and medulloblastoma entity. No prospective data on the feasibility of radiochemotherapy exist. The German Neuro-Oncology Working Group (NOA) performed a prospective descriptive multicenter single-arm phase II trial to evaluate feasibility and toxicity of radio-polychemotherapy.
The NOA-07 trial combined craniospinal irradiation with vincristine, followed by 8 cycles of cisplatin, lomustine, and vincristine. Adverse events, imaging and progression patterns, histological and genetic markers, health-related quality of life (HRQoL), and cognition were evaluated. Primary endpoint was the rate of toxicity-related treatment terminations after 4 chemotherapy cycles, and the toxicity profile. The feasibility goal was reached if at least 45% of patients received at least 4 cycles of maintenance chemotherapy.
Thirty patients were evaluable. Each 50% showed classic and desmoplastic/nodular histology. Sixty-seven percent were classified into the sonic hedgehog (SHH) subgroup without TP53 alterations, 13% in wingless (WNT), and 17% in non-WNT/non-SHH. Four cycles of chemotherapy were feasible in the majority (n = 21; 70.0%). Hematological side effects and polyneuropathy were prevalent toxicities. During the active treatment period, HRQoL and verbal fluency improved significantly. The 3-year event-free survival rate was 66.6% at the time of databank lock.
Radio-polychemotherapy did lead to considerable toxicity and a high amount of dose reductions throughout the first 4 chemotherapy cycles that may affect efficacy. Thus, we propose frequent patient surveillance using this regimen. Modifications of the regimen may increase feasibility of radio-polychemotherapy of adult patients with medulloblastoma.
成人髓母细胞瘤罕见,每百万人口中有 0.6 例。预后取决于临床因素和髓母细胞瘤实体。目前尚无关于放化疗可行性的前瞻性数据。德国神经肿瘤学工作组(NOA)进行了一项前瞻性描述性多中心单臂 II 期试验,以评估放化疗的可行性和毒性。
NOA-07 试验联合颅脊髓照射和长春新碱,随后进行 8 个周期顺铂、洛莫司汀和长春新碱化疗。评估不良事件、影像学和进展模式、组织学和遗传标志物、健康相关生活质量(HRQoL)和认知功能。主要终点是在第 4 个化疗周期后因毒性相关治疗终止的发生率和毒性特征。如果至少有 45%的患者接受了至少 4 个周期的维持化疗,则达到可行性目标。
30 例患者可评估。各有 50%表现为经典型和促结缔组织增生型/结节型组织学。67%的患者被归入无 TP53 改变的 sonic hedgehog(SHH)亚组,13%归入 wingless(WNT)亚组,17%归入非 WNT/非 SHH 亚组。在大多数患者中(n=21;70.0%),第 4 个化疗周期是可行的。血液学副作用和多发性神经病是常见的毒性。在积极治疗期间,HRQoL 和言语流畅性显著改善。数据锁定时,3 年无事件生存率为 66.6%。
放化疗确实导致了相当大的毒性和前 4 个化疗周期内大量的剂量减少,这可能会影响疗效。因此,我们建议在使用该方案时对患者进行频繁监测。该方案的修改可能会增加成人髓母细胞瘤放化疗的可行性。