Prognostic factors in adult patients with medulloblastoma.

IF 2.5 Q2 CLINICAL NEUROLOGY
Neuro-oncology practice Pub Date : 2025-09-01 eCollection Date: 2026-02-01 DOI:10.1093/nop/npaf084
Ytel Garcilazo-Reyes, Pierre Dal Col, Franck Bielle, Karima Mokhtari, Loïc Feuvret, Julian Jacob, Alberto Duran-Peña, Laurent Capelle, Julien Savatovsky, Franck Bourdeaut, Julien Masliah-Planchon, Bernardo Cacho-Díaz, Khê Hoang-Xuan, Ahmed Idbaih, Florence Laigle-Donadey
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引用次数: 0

Abstract

Background: Medulloblastoma (MB) is a rare tumor in adults, with treatment strategies derived largely from pediatric data. Prognostic factors have not been uniformly defined in adults to date.

Methods: We retrospectively reviewed the medical records of 89 adult MB patients treated between 1995 and 2019 in our institution. Patient's characteristics, disease features, and treatment modalities were analyzed for prognostic factors using univariate and multivariate analysis.

Results: Of the 89 patients, 66% were male. Most MBs were in the cerebellum (48%), with desmoplastic/nodular histology (43%), Sonic Hedgehog molecular type (79%), and M0 Chang´s stage (72%). Intermediate- and high-risk MBs were identified in ~46% and ~47% of cases, respectively. Complete/near complete tumor resection was achieved in 62% of cases. Surgery followed by chemoradiotherapy (CT/RT) was the most frequent treatment (76%) with carboplatin-based regimens used in 70% of cases. After the first-line treatment, complete response (CR) was achieved in 80% of patients. Median overall survival (mOS) was 124.4 months (95%CI 68.5-180.1) and the median progression free survival (mPFS) was 30.5 months (95%CI 13.5-47.5), the 5-year OS was 67% and the 5-year PFS was 51%. In multivariate analysis, Chang´s stage ≥ M2 metastatic classification (P = .001), RT without CT in first line setting (P = .005), and craniospinal RT < 30 Gy (P = .015) were associated with worse survival outcomes.

Conclusions: Chang's stage ≥ M2, first-line treatment lacking CT, and first-line treatment with craniospinal RT < 30 Gy were significant predictors of poor survival. Chemoradiotherapy with craniospinal RT ≥ 30 Gy improved survival outcomes.

成神经管细胞瘤成年患者预后因素分析。
背景:髓母细胞瘤(MB)是一种罕见的成人肿瘤,其治疗策略主要来源于儿科数据。迄今为止,成人的预后因素尚未统一定义。方法:回顾性分析我院1995年至2019年收治的89例成年MB患者的病历。使用单因素和多因素分析分析患者的特征、疾病特征和治疗方式,以确定预后因素。结果:89例患者中,男性占66%。大多数MBs发生在小脑(48%),伴有组织增生/结节组织学(43%),Sonic Hedgehog分子型(79%)和M0 Chang ' s分期(72%)。中度和高风险的MBs分别在46%和47%的病例中被确定。62%的病例实现了完全或接近完全的肿瘤切除。手术后放化疗(CT/RT)是最常见的治疗方法(76%),70%的病例使用基于卡铂的方案。在一线治疗后,80%的患者达到完全缓解(CR)。中位总生存期(mOS)为124.4个月(95%CI 68.5-180.1),中位无进展生存期(mPFS)为30.5个月(95%CI 13.5-47.5), 5年OS为67%,5年PFS为51%。在多因素分析中,Chang ' s分期≥M2转移分类(P =。001),不加CT的一线放疗(P = 0.001)。005),颅脊髓RT P =。015)与较差的生存结果相关。结论:Chang's分期≥M2,一线治疗无CT,一线治疗颅脊髓RT
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来源期刊
Neuro-oncology practice
Neuro-oncology practice CLINICAL NEUROLOGY-
CiteScore
5.30
自引率
11.10%
发文量
92
期刊介绍: Neuro-Oncology Practice focuses on the clinical aspects of the subspecialty for practicing clinicians and healthcare specialists from a variety of disciplines including physicians, nurses, physical/occupational therapists, neuropsychologists, and palliative care specialists, who have focused their careers on clinical patient care and who want to apply the latest treatment advances to their practice. These include: Applying new trial results to improve standards of patient care Translating scientific advances such as tumor molecular profiling and advanced imaging into clinical treatment decision making and personalized brain tumor therapies Raising awareness of basic, translational and clinical research in areas of symptom management, survivorship, neurocognitive function, end of life issues and caregiving
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