Chaskis E, Minichini V, Luce S, Devriendt D, Goldman S, De Witte O, Sadeghi N, Lefranc F
Services de neurochirurgie, hôpital Erasme, route de Lennik, 808, 1070 Bruxelles, Belgique.
Services d'oncologie médicale, hôpital Erasme, route de Lennik, 808, 1070 Bruxelles, Belgique.
Neurochirurgie. 2017 Sep;63(4):297-301. doi: 10.1016/j.neuchi.2017.05.002. Epub 2017 Sep 4.
Grade II intramedullary astrocytomas are rare tumors. Despite a well-defined role of adjuvant temozolomide chemotherapy for brain gliomas, the contribution of this therapy for intramedullary gliomas is not yet clearly defined.
We retrospectively analyzed the data of 5 adult patients treated with temozolomide between 2008 and 2015 for a grade II intramedullary astrocytoma with progression after surgery.
Five patients from 19 to 70 years of age (median, 37years) underwent a second surgery for the progression of a grade II intramedullary astrocytoma (median progression-free survival 26months [8-90]). All tumors remained grade II. Due to a second clinical or/and radiological tumor progression, the patients were treated with temozolomide after a 37months median progression-free survival (5-66). All patients received at minimum 12 cycles (mean 14 ± 5; range 12-24) of temozolomide (150-200mg/m/day, 5days/28days). All patients were alive after a 10-year median follow-up after diagnosis (6-13). All patients were able to walk except one, who was previously in McCormick autonomy grade IV before chemotherapy. The McCormick autonomy rating after temozolomide was stable for 4 patients and improved for 1 patient. The treatment was delayed once for hematological toxicity.
Temozolomide stabilized all 5 patients without any major toxicity. Based on this experience that needs to be confirmed, we consider that temozolomide should be envisaged within the therapeutic arsenal for progressive intramedullary grade II astrocytomas.
II级髓内星形细胞瘤是罕见肿瘤。尽管辅助替莫唑胺化疗在脑胶质瘤治疗中作用明确,但该疗法对髓内胶质瘤的作用尚未明确界定。
我们回顾性分析了2008年至2015年间5例接受替莫唑胺治疗的成年患者的数据,这些患者患有II级髓内星形细胞瘤且术后病情进展。
5例年龄在19至70岁(中位年龄37岁)的患者因II级髓内星形细胞瘤进展接受了二次手术(中位无进展生存期26个月[8 - 90])。所有肿瘤仍为II级。由于出现第二次临床或/和影像学肿瘤进展,患者在中位无进展生存期37个月(5 - 66)后接受了替莫唑胺治疗。所有患者至少接受了12个周期(平均14±5;范围12 - 24)的替莫唑胺治疗(150 - 200mg/m²/天,5天/28天)。诊断后中位随访10年(6 - 13),所有患者均存活。除1例患者化疗前处于麦考密克自主分级IV级外,所有患者均能行走。替莫唑胺治疗后,4例患者的麦考密克自主评分稳定,1例患者有所改善。治疗因血液学毒性延迟了一次。
替莫唑胺使所有5例患者病情稳定,且无任何严重毒性。基于这一有待证实的经验,我们认为对于进展性II级髓内星形细胞瘤,应将替莫唑胺纳入治疗方案中。