van Dijck Jeroen T J M, Ardon Hilko, Balvers Rutger K, Bos Eelke M, Bosscher Lisette, Brouwers H Bart, Ho Vincent K Y, Hovinga Koos, Kwee Lesley, Ter Laan Mark, Nabuurs Rob J A, Robe Pierre A J T, van Geest Sarita, van der Veer Olivier, Verburg Niels, Wagemakers Michiel, de Witt Hamer Philip C, Rodriguez Girondo Mar, Nandoe Tewarie Rishi D S
Department of Neurosurgery, Haaglanden Medical Centre, The Hague, The Netherlands.
Department of Neurosurgery, Leiden University Medical Center, Leiden, The Netherlands.
J Neurooncol. 2025 May 23. doi: 10.1007/s11060-025-05080-3.
Glioblastoma is the most common and treatment-resistant primary malignant brain tumor, with high morbidity and mortality despite standard treatment protocols. This study aims to evaluate survival and prognostic factors, and introduce two pragmatic prognostic models to inform individualized, patient-centered decision-making, using a large Dutch registry.
We analyzed a prospective cohort of 7621 patients (2012-2022) in 12 Dutch centers via the Dutch Quality Registry Neurosurgery. Univariate analysis of prognostic factors, Kaplan-Meier survival curves, and funnel plots comparing center performance (30-day and 2-year mortality) were conducted. Two prognostic models using multivariate Cox regression were developed.
Glioblastoma incidence was 3.9/100.000 in The Netherlands. Overall, 30-day mortality was 5.1% and 2-year survival 17.8%. Overall median survival was 10.4 months, with 4.6 months after biopsy and 12.9 months post-resection. Poorer survival correlated with older age, higher ASA classification, lower Karnofsky Performance Status, biopsy over resection (HR 0.49, 95% CI 0.47-0.52), and postoperative complications (HR 1.57 95% CI 1.39-1.79). MGMT promotor methylation (HR 0.58, 95% CI 0.53-0.63) and adjuvant treatment were linked to lower mortality. Treatment variation and outcomes were within expected ranges; surgical volume did not affect survival. The prognostic models had C-indices of 0.704 (6-month) and 0.721 (2-year).
Surgical resection and adjuvant therapy improved survival, but prognosis remained poor. Age, premorbid condition, treatment and molecular markers influenced survival. Center variations were within expected range, and higher surgical volume did not improve outcomes. The developed prognostic models could potentially inform clinicians, pending external validation.
胶质母细胞瘤是最常见且难以治疗的原发性恶性脑肿瘤,尽管有标准治疗方案,但发病率和死亡率仍很高。本研究旨在评估生存率和预后因素,并引入两种实用的预后模型,以通过荷兰的一个大型登记处为个体化、以患者为中心的决策提供依据。
我们通过荷兰神经外科质量登记处分析了荷兰12个中心的7621例患者(2012 - 2022年)的前瞻性队列。对预后因素进行单因素分析、绘制Kaplan - Meier生存曲线,并绘制漏斗图比较各中心的表现(30天和2年死亡率)。开发了两种使用多变量Cox回归的预后模型。
荷兰胶质母细胞瘤发病率为3.9/100000。总体而言,30天死亡率为5.1%,2年生存率为17.8%。总体中位生存期为10.4个月,活检后为4.6个月,切除术后为12.9个月。较差的生存率与年龄较大、美国麻醉医师协会(ASA)分级较高、卡诺夫斯基功能状态较低、活检而非切除(风险比[HR]0.49,95%置信区间[CI]0.47 - 0.52)以及术后并发症(HR 1.57,95% CI 1.39 - 1.79)相关。O6 - 甲基鸟嘌呤 - DNA甲基转移酶(MGMT)启动子甲基化(HR 0.58,95% CI 0.53 - 0.63)和辅助治疗与较低死亡率相关。治疗差异和结果在预期范围内;手术量不影响生存率。预后模型的C指数在6个月时为0.704,2年时为0.721。
手术切除和辅助治疗可提高生存率,但预后仍然较差。年龄、病前状况、治疗和分子标志物影响生存率。各中心差异在预期范围内,手术量增加并未改善结果。所开发的预后模型在有待外部验证的情况下可能会为临床医生提供参考。