Rajkumar S V, Buckner J C, Schomberg P J, Cascino T L, Burch P A, Dinapoli R P
Division of Medical Oncology, Mayo Clinic and Foundation, Rochester, MN 55905, USA.
Int J Radiat Oncol Biol Phys. 1998 Jan 15;40(2):297-302. doi: 10.1016/s0360-3016(97)00739-6.
A Phase I study to determine the safety, toxicity, and maximum tolerated dose (MTD) of carmustine (BCNU) and interferon alpha-2a (IFN-a) when combined with radiation as initial therapy in high-grade glioma.
Patients with newly diagnosed Grade 3 or 4 astrocytoma, oligoastrocytoma, or gliosarcoma were enrolled after surgery. All received radiation therapy to the brain (64.8 Gy/36 fractions), combined with a single dose of BCNU (200 mg/m2) at the start of radiation. Chemotherapy after completing radiation consisted of BCNU 150 mg/m2 once every 7 weeks, and IFN-a 12 x 10(6) units/m2 subcutaneously Days 1-3 each week of a 7-week cycle. Subsequent dose modification was based on constitutional symptoms for IFN-a and on myelosuppression for BCNU.
Fifteen patients were entered on the study. Four were excluded because they did not receive IFN-a (3 refused treatment and 1 patient left the study due to multiple medical problems). Eleven were evaluable for toxicity and efficacy. Nonhematological toxicity, mainly lethargy and flu-like symptoms, were dose-limiting for IFN-a. After the first 6 patients were treated per the initial protocol, the frequency of IFN-a administration was decreased to Days 1-3 on weeks 1, 3, and 5 of the 7-week cycle for 5 additional patients. Lethargy, fever, chills, myalgias, alopecia, and anorexia occurred in all patients. Other toxicities included nausea and vomiting (91%), central-nervous-system depression or mood changes (64%), headaches (55%), and elevation of liver enzymes (36%). Grade 3-4 leukopenia occurred in 4 (45%) of 11 patients, and Grade 3-4 thrombocytopenia in 3 (27%) of 11 patients. Due to myelosuppressive effects, BCNU dose was not escalated. Median survival of the cohort was 44 months. Objective responses occurred in 5 (56%) of 9 patients and median duration of response was 33 months. The MTD of this combination after radiation therapy is IFN-a 12 x 10(6) units/m2 Days 1-3, on Weeks 1, 3, and 5 of a 7-week cycle and BCNU 150 mg/m2 Day 1, every 7 weeks.
Treatment with radiation, IFN-a, and BCNU is feasible and effective in patients with high-grade gliomas, although constitutional symptoms from IFN-a are substantial.
进行一项I期研究,以确定卡莫司汀(BCNU)和干扰素α-2a(IFN-α)与放疗联合作为高级别胶质瘤初始治疗时的安全性、毒性和最大耐受剂量(MTD)。
新诊断为3级或4级星形细胞瘤、少突星形细胞瘤或胶质肉瘤的患者在手术后入组。所有患者均接受脑部放射治疗(64.8 Gy/36次分割),并在放疗开始时联合单次剂量的BCNU(200 mg/m²)。放疗完成后的化疗包括每7周一次的BCNU 150 mg/m²,以及在7周周期的每周第1 - 3天皮下注射IFN-α 12×10⁶单位/m²。后续剂量调整基于IFN-α的全身症状和BCNU的骨髓抑制情况。
15名患者进入该研究。4名患者被排除,因为他们未接受IFN-α(3名拒绝治疗,1名因多种医疗问题退出研究)。11名患者可评估毒性和疗效。非血液学毒性主要为嗜睡和流感样症状,是IFN-α的剂量限制性毒性。按照初始方案治疗前6名患者后,另外5名患者的IFN-α给药频率降至7周周期的第1、3和5周的第1 - 3天。所有患者均出现嗜睡、发热、寒战、肌痛、脱发和厌食。其他毒性包括恶心和呕吐(91%)、中枢神经系统抑制或情绪变化(64%)、头痛(55%)以及肝酶升高(36%)。11名患者中有4名(45%)出现3 - 4级白细胞减少,11名患者中有3名(27%)出现3 - 4级血小板减少。由于骨髓抑制作用,BCNU剂量未增加。该队列的中位生存期为44个月。9名患者中有5名(56%)出现客观缓解,中位缓解持续时间为33个月。放疗后该联合方案的MTD为7周周期的第1、3和5周的第1 - 3天给予IFN-α 12×10⁶单位/m²,每7周第1天给予BCNU 150 mg/m²。
放疗、IFN-α和BCNU联合治疗对高级别胶质瘤患者是可行且有效的,尽管IFN-α引起的全身症状较为明显。