Harald Krenzlin, Dragan Jankovic, Alice Dauth, Felipa Lange, Martin Wetzel, Leon Schmidt, Insa Janssen, Christoph Richter, Marcus Stockinger, Heinz Schmidberger, Marc A Brockmann, Clemens Sommer, Bernhard Meyer, Naureen Keric, Florian Ringel
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Primary outcome parameters were extent of resection (EOR) using the 2021 RANO criteria, progression free- and overall survival.</p><p><strong>Results: </strong>A total of 483 patients with newly diagnosed glioblastoma (CNS WHO grade 4) were assessed. 134 patients presented with ML (72 multifocal (MF), 62 multicentric (MC)). The median PFS and OS did not differ among MC and MF glioblastomas. The EOR was a significant predictor of PFS and OS in ML glioblastoma. complete-, near total-, and subtotal resection significantly prolonged PFS (p < 0.0001) and OS (p < 0.0001) compared to biopsy alone. Standard radiotherapy (p = 0.045) and hypofractionated (p < 0.0001) radiotherapy and adjuvant treatment (Stupp protocol) prolonged PFS (p = 0.0012) and OS (p < 0.0001). In multivariate analysis Karnfosky performance score, EOR, and concomitant adjuvant treatment remained significant factors influencing OS. Propensity score matching of patients with ML and solitary lesion tumors showed similar PFS and OS (p = 0.08).</p><p><strong>Conclusion: </strong>The presented data suggests that glioblastomas with multiple lesions treated with multimodal therapy equal survival rates compared to patients with solitary lesion tumors can be achieved. 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引用次数: 0
摘要
目的:胶质母细胞瘤中存在多定位(ML)的情况十分罕见,且预后较差。本研究旨在评估多模式治疗对ML型胶质母细胞瘤患者无进展生存期(PFS)和总生存期(OS)的影响:研究对象包括2008年1月1日至2020年12月31日期间在德国两大神经外科就诊的中枢神经系统WHO 4级胶质母细胞瘤伴ML患者。主要结果参数为采用2021年RANO标准的切除范围(EOR)、无进展和总生存期:共评估了 483 名新确诊的胶质母细胞瘤(中枢神经系统 WHO 4 级)患者。134名患者出现ML(72例多灶(MF),62例多中心(MC))。MC和MF胶质母细胞瘤的中位生存期和OS没有差异。EOR是预测ML型胶质母细胞瘤PFS和OS的重要指标,完全切除、近全切除和次全切除可显著延长PFS(P 结论:EOR是预测ML型胶质母细胞瘤PFS和OS的重要指标,完全切除、近全切除和次全切除可显著延长PFS:所提供的数据表明,多病灶胶质母细胞瘤在接受多模式疗法治疗后,可以获得与单发病灶肿瘤患者相同的生存率。这些结果反映了对这一特殊且往往被边缘化的患者群体采取同样积极的最大治疗努力的重要性。
Multimodal treatment of glioblastoma with multiple lesions - a multi-center retrospective analysis.
Objective: The presence of multiple localizations (ML) in glioblastoma is rare and associated with perceived poor prognosis. The aim of this study is to evaluate the impact of a multimodal treatment on progression-free survival (PFS) and overall survival (OS) in ML glioblastoma.
Methods: Patients presenting with CNS WHO grade 4 glioblastoma with ML to 2 major German Departments of Neurosurgery between January 1st, 2008, to December 31st, 2020 were included in this study. Primary outcome parameters were extent of resection (EOR) using the 2021 RANO criteria, progression free- and overall survival.
Results: A total of 483 patients with newly diagnosed glioblastoma (CNS WHO grade 4) were assessed. 134 patients presented with ML (72 multifocal (MF), 62 multicentric (MC)). The median PFS and OS did not differ among MC and MF glioblastomas. The EOR was a significant predictor of PFS and OS in ML glioblastoma. complete-, near total-, and subtotal resection significantly prolonged PFS (p < 0.0001) and OS (p < 0.0001) compared to biopsy alone. Standard radiotherapy (p = 0.045) and hypofractionated (p < 0.0001) radiotherapy and adjuvant treatment (Stupp protocol) prolonged PFS (p = 0.0012) and OS (p < 0.0001). In multivariate analysis Karnfosky performance score, EOR, and concomitant adjuvant treatment remained significant factors influencing OS. Propensity score matching of patients with ML and solitary lesion tumors showed similar PFS and OS (p = 0.08).
Conclusion: The presented data suggests that glioblastomas with multiple lesions treated with multimodal therapy equal survival rates compared to patients with solitary lesion tumors can be achieved. The results reflect the importance of an equally aggressive maximal treatment effort in this particular and often marginalized group of patients.
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.