Amelot Aymeric, Terrier Louis-Marie, Cognacq Gabrielle, Jecko Vincent, Marlier Benoit, Seizeur Romuald, Emery Evelyne, Bauchet Luc, Roualdes Vincent, Voirin Jimmy, Joubert Christophe, Mandonnet Emmanuel, Lemnos Leslie, Mathon Bertrand, Le Reste Pierre-Jean, Coca Andres, Petit Antoine, Rigau Valérie, Mokhtari Karima, Rousseau Audrey, Metellus Philippe, Figarella-Branger Dominique, Gauchotte Guillaume, Farah Kaissar, Pallud Johan, Zemmoura Ilyess
Department of Neurosurgery, CHRU de Tours, Tours, France.
Service de Neurochirurgie, CHRU Bretonneau, 2 Boulevard Tonnellé, Tours Cedex 9, 37044, Tours, France.
J Neurooncol. 2023 Apr;162(2):373-382. doi: 10.1007/s11060-023-04298-3. Epub 2023 Mar 29.
Spinal cord metastasis arising from an intracranial glioblastoma is a rare and late event during the natural course of the disease. These pathological entities remain poorly characterized. This study aimed to identify and investigate the timeline, clinical and imaging findings, and prognostic factors of spinal cord metastasis from a glioblastoma.
Consecutive histopathological cases of spinal cord metastasis from glioblastomas in adults entered in the French nationwide database between January 2004 and 2016 were screened.
Overall, 14 adult patients with a brain glioblastoma (median age 55.2 years) and harboring a spinal cord metastasis were included. The median overall survival as 16.0 months (range, 9.8-22.2). The median spinal cord Metastasis Free Survival (time interval between the glioblastoma diagnosis and the spinal cord metastasis diagnosis) was 13.6 months (range, 0.0-27.9). The occurrence of a spinal cord metastasis diagnosis greatly impacted neurological status: 57.2% of patients were not ambulatory, which contributed to dramatically decreased Karnofsky Performance Status (KPS) scores (12/14, 85.7% with a KPS score ≤ 70). The median overall survival following spinal cord metastasis was 3.3 months (range, 1.3-5.3). Patients with a cerebral ventricle effraction during the initial brain surgery had a shorter spinal cord Metastasis Free Survival (6.6 vs 18.3 months, p = 0.023). Out of the 14 patients, eleven (78.6%) had a brain IDH-wildtype glioblastoma.
Spinal cord metastasis from a brain IDH-wildtype glioblastoma has a poor prognosis. Spinal MRI can be proposed during the follow-up of glioblastoma patients especially those who have benefited from cerebral surgical resection with opening of the cerebral ventricles.
颅内胶质母细胞瘤引起的脊髓转移是该疾病自然病程中罕见的晚期事件。这些病理实体的特征仍不明确。本研究旨在确定并研究胶质母细胞瘤脊髓转移的时间线、临床和影像学表现以及预后因素。
筛选2004年1月至2016年期间录入法国全国数据库的成人间质母细胞瘤脊髓转移的连续组织病理学病例。
共纳入14例患有脑胶质母细胞瘤(中位年龄55.2岁)并伴有脊髓转移的成年患者。中位总生存期为16.0个月(范围9.8 - 22.2个月)。中位无脊髓转移生存期(胶质母细胞瘤诊断与脊髓转移诊断之间的时间间隔)为13.6个月(范围0.0 - 27.9个月)。脊髓转移诊断的出现对神经状态有很大影响:57.2%的患者无法行走,这导致卡氏功能状态评分(KPS)显著降低(14例中有12例,85.7%的KPS评分≤70)。脊髓转移后的中位总生存期为3.3个月(范围1.3 - 5.3个月)。初次脑手术期间出现脑室破裂的患者无脊髓转移生存期较短(6.6个月对18.3个月,p = 0.023)。14例患者中,11例(78.6%)患有脑异柠檬酸脱氢酶(IDH)野生型胶质母细胞瘤。
脑IDH野生型胶质母细胞瘤的脊髓转移预后较差。在胶质母细胞瘤患者的随访过程中,尤其是那些接受了脑室开放的脑外科切除术的患者,可考虑进行脊髓磁共振成像检查。