Jeroen T J M van Dijck, Hilko Ardon, Rutger K Balvers, Eelke M Bos, Lisette Bosscher, H Bart Brouwers, Vincent K Y Ho, Koos Hovinga, Lesley Kwee, Mark Ter Laan, Rob J A Nabuurs, Pierre A J T Robe, Sarita van Geest, Olivier van der Veer, Niels Verburg, Michiel Wagemakers, Philip C de Witt Hamer, Mar Rodriguez Girondo, Rishi D S Nandoe Tewarie
{"title":"胶质母细胞瘤的生存预测:来自荷兰神经外科质量登记处的10年随访。","authors":"Jeroen T J M van Dijck, Hilko Ardon, Rutger K Balvers, Eelke M Bos, Lisette Bosscher, H Bart Brouwers, Vincent K Y Ho, Koos Hovinga, Lesley Kwee, Mark Ter Laan, Rob J A Nabuurs, Pierre A J T Robe, Sarita van Geest, Olivier van der Veer, Niels Verburg, Michiel Wagemakers, Philip C de Witt Hamer, Mar Rodriguez Girondo, Rishi D S Nandoe Tewarie","doi":"10.1007/s11060-025-05080-3","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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).</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":16425,"journal":{"name":"Journal of Neuro-Oncology","volume":" ","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Survival prediction in glioblastoma: 10-year follow-up from the Dutch Neurosurgery Quality Registry.\",\"authors\":\"Jeroen T J M van Dijck, Hilko Ardon, Rutger K Balvers, Eelke M Bos, Lisette Bosscher, H Bart Brouwers, Vincent K Y Ho, Koos Hovinga, Lesley Kwee, Mark Ter Laan, Rob J A Nabuurs, Pierre A J T Robe, Sarita van Geest, Olivier van der Veer, Niels Verburg, Michiel Wagemakers, Philip C de Witt Hamer, Mar Rodriguez Girondo, Rishi D S Nandoe Tewarie\",\"doi\":\"10.1007/s11060-025-05080-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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).</p><p><strong>Conclusion: </strong>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.</p>\",\"PeriodicalId\":16425,\"journal\":{\"name\":\"Journal of Neuro-Oncology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-05-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Neuro-Oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s11060-025-05080-3\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neuro-Oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s11060-025-05080-3","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
目的:胶质母细胞瘤是最常见和治疗抵抗的原发性恶性脑肿瘤,尽管有标准的治疗方案,但其发病率和死亡率都很高。本研究旨在评估生存和预后因素,并引入两种实用的预后模型,为个性化,以患者为中心的决策提供信息,使用大型荷兰注册。方法:通过荷兰神经外科质量注册中心,我们分析了来自12个荷兰中心的7621例患者(2012-2022)的前瞻性队列。对预后因素、Kaplan-Meier生存曲线和比较中心表现(30天和2年死亡率)的漏斗图进行单因素分析。采用多变量Cox回归建立了两种预后模型。结果:荷兰胶质母细胞瘤发病率为3.9/10万。总体而言,30天死亡率为5.1%,2年生存率为17.8%。总中位生存期为10.4个月,活检后4.6个月,切除后12.9个月。较差的生存率与年龄较大、ASA分级较高、Karnofsky性能状态较低、活检优于切除(HR 0.49, 95% CI 0.47-0.52)和术后并发症(HR 1.57, 95% CI 1.39-1.79)相关。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。治疗变化和结果在预期范围内;手术量对生存率无影响。预后模型的c指数分别为0.704(6个月)和0.721(2年)。结论:手术切除和辅助治疗改善了患者的生存,但预后仍然较差。年龄、病前状况、治疗和分子标记影响生存率。中心变化在预期范围内,更高的手术量并没有改善结果。开发的预后模型可能会告知临床医生,等待外部验证。
Survival prediction in glioblastoma: 10-year follow-up from the Dutch Neurosurgery Quality Registry.
Purpose: 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.
Methods: 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.
Results: 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).
Conclusion: 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.
期刊介绍:
The Journal of Neuro-Oncology is a multi-disciplinary journal encompassing basic, applied, and clinical investigations in all research areas as they relate to cancer and the central nervous system. It provides a single forum for communication among neurologists, neurosurgeons, radiotherapists, medical oncologists, neuropathologists, neurodiagnosticians, and laboratory-based oncologists conducting relevant research. The Journal of Neuro-Oncology does not seek to isolate the field, but rather to focus the efforts of many disciplines in one publication through a format which pulls together these diverse interests. More than any other field of oncology, cancer of the central nervous system requires multi-disciplinary approaches. To alleviate having to scan dozens of journals of cell biology, pathology, laboratory and clinical endeavours, JNO is a periodical in which current, high-quality, relevant research in all aspects of neuro-oncology may be found.