Yazici Gozde, Zorlu Faruk, Cengiz Mustafa, Ozyigit Gokhan, Eren Gulnihan, Yüce Deniz, Varan Ali, Akyuz Canan, Akalan Nejat, Gurkaynak Murat
Department of Radiation Oncology, School of Medicine, Hacettepe University, Sihhiye, 06100, Ankara, Turkey.
Department of Preventive Oncology, School of Medicine, Hacettepe University, Ankara, Turkey.
Childs Nerv Syst. 2016 Feb;32(2):291-7. doi: 10.1007/s00381-015-2980-3. Epub 2015 Dec 17.
The aim of this study was to report the outcome in children with high-grade astrocytoma outside the brain stem and spinal cord that were treated at a single center.
The study included 26 patients with anaplastic astrocytoma and 37 patients with glioblastoma; all patients were aged ≤18 years. At initial diagnosis, 18 of the patients with glioblastoma received only temozolomide (TMZ), 14 received other chemotherapies, and 5 did not receive any chemotherapy. Among the patients with anaplastic astrocytoma, 9 received TMZ, 9 received other chemotherapy regimens, and 8 patients did not receive any chemotherapy. The median radiotherapy dose in all patients was 60 Gy.
Median age of the patients was 12.5 years. Median overall survival was 20 months and mean progression-free survival was 4.7-11.3 months (median: 8 months) in all patients. Patients with a Karnofsky performance score (KPS) ≥70 had median overall survival of 32 months, versus 7 months in those with a KPS < 70. Patients aged <15 years had median survival of 38 months, versus 16 months in those aged 15-18 years. Patients with anaplastic astrocytoma that received TMZ, other chemotherapy regimens, and no chemotherapy had median survival of 21 months, 132 months, and 11 months, respectively. Patients with glioblastoma that received TMZ, other chemotherapy regimens, and no chemotherapy had median survival of 32 months, 12 months, and 8 months, respectively.
In the present study, patients with anaplastic astrocytoma treated with chemotherapy protocols other than TMZ had the longest OS; however, in the glioblastoma group, OS was 32 months in those treated with standard TMZ and 12 months in those treated with other protocols (P = 0.493). Although TMZ is less toxic than PCV, it was not shown to be superior.
本研究旨在报告在单一中心接受治疗的脑干和脊髓外高级别星形细胞瘤患儿的治疗结果。
该研究纳入了26例间变性星形细胞瘤患者和37例胶质母细胞瘤患者;所有患者年龄均≤18岁。在初次诊断时,18例胶质母细胞瘤患者仅接受替莫唑胺(TMZ)治疗,14例接受其他化疗,5例未接受任何化疗。在间变性星形细胞瘤患者中,9例接受TMZ治疗,9例接受其他化疗方案,8例未接受任何化疗。所有患者的中位放疗剂量为60 Gy。
患者的中位年龄为12.5岁。所有患者的中位总生存期为20个月,平均无进展生存期为4.7 - 11.3个月(中位值:8个月)。卡诺夫斯基表现评分(KPS)≥70的患者中位总生存期为32个月,而KPS < 70的患者为7个月。年龄<15岁的患者中位生存期为38个月,而15 - 18岁的患者为16个月。接受TMZ、其他化疗方案和未接受化疗的间变性星形细胞瘤患者的中位生存期分别为21个月、132个月和11个月。接受TMZ、其他化疗方案和未接受化疗的胶质母细胞瘤患者的中位生存期分别为32个月、12个月和8个月。
在本研究中,接受TMZ以外化疗方案治疗的间变性星形细胞瘤患者总生存期最长;然而,在胶质母细胞瘤组中,接受标准TMZ治疗的患者总生存期为32个月,接受其他方案治疗的患者为12个月(P = 0.493)。尽管TMZ的毒性低于PCV,但未显示出其具有优越性。