Rudà Roberta, Bosa Chiara, Magistrello Michela, Franchino Federica, Pellerino Alessia, Fiano Valentina, Trevisan Morena, Cassoni Paola, Soffietti Riccardo
Department of Neuro-Oncology, University and City of Health and Science Hospital, Torino, Italy (R.R., C.B., M.M., F.F., A.P., R.S.); Department of Clinical Epidemiology, University and City of Health and Science University Hospital, Torino, Italy (V.F., M.T.); Department of Biomedical Sciences and Oncology, University and City of Health and Science Hospital, Torino 10126, Italy (P.C.).
Neuro Oncol. 2016 Feb;18(2):261-8. doi: 10.1093/neuonc/nov167. Epub 2015 Aug 30.
Few data are available on temozolomide (TMZ) in ependymomas.We investigated the response, survival, and correlation with MGMT promoter methylation in a cohort of patients with adult intracranial ependymoma receiving TMZ as salvage therapy after failure of surgery and radiotherapy.
We retrieved clinical information from the institutional database and follow-up visits, and response to TMZ on MRI was evaluated according to the MacDonald criteria.
Eighteen patients (median age, 42 y), with either WHO grade III (10) or grade II (8) ependymoma were evaluable. Tumor location at diagnosis was supratentorial in 11 patients and infratentorial in 7. Progression before TMZ was local in 11 patients, local and spinal in 6 patients, and spinal only in one patient. A median of 8 cycles of TMZ (1-24) was administered. Response to TMZ consisted of complete response (CR) in one (5%) patient, partial response (PR) in 3 (17%) patients, stable disease (SD) in 7 (39%) patients, and progressive disease (PD) in 7 (39%) patients. Maximum response occurred after 3, 10, 14, and 15 cycles, respectively, with neurological improvement in 2 patients. All 4 responding patients were chemotherapy naïve. Both anaplastic (2) and grade II (2) tumors responded. Median progression-free survival and overall survival were 9.69 months (95% CI, 3.22-30.98) and 30.55 months (95% CI, 12.85-52.17), respectively. MGMT methylation was available in 11 patients and was not correlated with response or outcome.
TMZ has a role in recurrent chemo-naïve adult patients with intracranial ependymoma, regardless of tumor grade and MGMT methylation. We suggest that, after failure of surgery and radiotherapy, TMZ should be considered as a possible first-line treatment for recurrent ependymoma.
关于替莫唑胺(TMZ)用于室管膜瘤治疗的数据较少。我们对一组接受TMZ作为手术和放疗失败后的挽救治疗的成年颅内室管膜瘤患者的反应、生存情况以及与O⁶-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子甲基化的相关性进行了研究。
我们从机构数据库和随访中获取临床信息,并根据麦克唐纳标准评估MRI上对TMZ的反应。
18例患者(中位年龄42岁)可进行评估,其中世界卫生组织(WHO)Ⅲ级室管膜瘤10例,Ⅱ级室管膜瘤8例。诊断时肿瘤位于幕上11例,幕下7例。TMZ治疗前进展为局部进展的患者11例,局部和脊髓进展的患者6例,仅脊髓进展的患者1例。TMZ的中位给药周期数为8个周期(1 - 24个周期)。对TMZ的反应包括1例(5%)患者完全缓解(CR),3例(17%)患者部分缓解(PR),7例(39%)患者疾病稳定(SD),7例(39%)患者疾病进展(PD)。最大反应分别在第3、10、14和15个周期后出现,2例患者神经功能改善。所有4例有反应的患者均未接受过化疗。间变性(2例)和Ⅱ级(2例)肿瘤均有反应。中位无进展生存期和总生存期分别为9.69个月(95%置信区间[CI],3.22 - 30.98)和30.55个月(95% CI,12.85 - 52.17)。11例患者可检测MGMT甲基化情况,其与反应或结局无关。
TMZ在复发的未接受过化疗的成年颅内室管膜瘤患者中具有一定作用,无论肿瘤分级和MGMT甲基化情况如何。我们建议,在手术和放疗失败后,TMZ应被视为复发性室管膜瘤可能的一线治疗方法。