Jeremic B, Grujicic D, Antunovic V, Djuric L, Shibamoto Y
Department of Oncology, University Hospital, Kragujevac, Yugoslavia.
Am J Clin Oncol. 1995 Oct;18(5):449-53. doi: 10.1097/00000421-199510000-00019.
Sixty-four adult patients with malignant glioma entered into a Phase II study on the use of accelerated hyperfractionated radiation therapy. Histology included anaplastic astrocytoma (AA) in 15 patients and glioblastoma multiforme (GBM) in 49 patients. Treatment consisted of radiation therapy doses of 66 Gy in 44 fractions in 22 treatment days in 4.5 weeks, fractions of 1.5 Gy, b.i.d. 1,3-bis(2-chlorethyl)-1-nitrosourea (BCNU) 80 mg/m2 and hydroxyurea 800 mg/m2 were both given on treatment days 1, 6, 11, 16, and 21 during the irradiation course. Median survival time for all 64 patients is 61 weeks (range; 12-163 weeks) from the date of starting irradiation. Median time to tumor progression (MTP) for GBM patients is 31 weeks, and 1-year and 3-year progression-free survival (PFS) are 16% and 0%, respectively, while MTP for AA patients is not attained yet, and 1-year and 3-year PFS are 100% and 73%, respectively. On univariate analysis of prognostic factors for GBM patients, younger age, total or subtotal tumor removal, and frontal tumor location are associated with a better prognosis. A multivariate analysis confirmed the importance of the extent of surgery and tumor site and revealed the interfraction interval (4.5-5.0 hours vs 5.5-6.0 hours, p = .041) as an important prognostic factor. Acute and late toxicity is not increased. Longer follow-up and more patients are needed to evaluate tumor control and toxicity in AA patients.
64例成年恶性胶质瘤患者进入了一项关于加速超分割放射治疗应用的II期研究。组织学类型包括15例间变性星形细胞瘤(AA)和49例多形性胶质母细胞瘤(GBM)。治疗包括在4.5周的22个治疗日中,分44次给予66 Gy的放射治疗剂量,每次分割剂量为1.5 Gy,每日2次。在放疗过程中的第1、6、11、16和21天给予1,3-双(2-氯乙基)-1-亚硝基脲(BCNU)80 mg/m²和羟基脲800 mg/m²。从开始放疗之日起,所有64例患者的中位生存时间为61周(范围:12 - 163周)。GBM患者的肿瘤进展中位时间(MTP)为31周,1年和3年无进展生存率(PFS)分别为16%和0%,而AA患者的MTP尚未达到,1年和3年PFS分别为100%和73%。对GBM患者预后因素的单因素分析显示,年龄较小、肿瘤全切除或次全切除以及肿瘤位于额叶与较好的预后相关。多因素分析证实了手术范围和肿瘤部位的重要性,并揭示了分割间期(4.5 - 5.0小时与5.5 - 6.0小时,p = 0.041)是一个重要的预后因素。急性和晚期毒性并未增加。需要更长时间的随访和更多患者来评估AA患者的肿瘤控制情况和毒性。