Elliott T E, Buckner J C, Cascino T L, Levitt R, O'Fallon J R, Scheithauer B W
Duluth Clinic CCOP, Minnesota 55805.
J Neurooncol. 1991 Feb;10(1):27-30. doi: 10.1007/BF00151244.
Sixteen patients who developed CT or MRI scan evidence of recurrent diffuse astrocytoma after radiation therapy and nitrosourea-containing chemotherapy received ifosfamide (2500 mg/m2/day for 3 consecutive days) and mesna (500 mg/m2/dose, 5 doses/day for 3 consecutive days). Toxicity consisted primarily of leukopenia in that 60 percent of patients developed leukocyte nadirs less than 1500/mcL. Excessive somnolence occurred in three patients and may have contributed to a case of fatal pneumonia in one patient but was reversible in the other two. No patient had CT or MRI scan evidence of tumor regression. One patient remains stable at 11.3 + months, but all other patients developed evidence of progressive disease less than 6 months from initiation of therapy. The median times to tumor progression and death were 2.0 and 4.8 months, respectively. In conclusion, while ifosfamide and mesna can be given safely at this dose and schedule, there is no evidence of antitumor effect. The degree of leukopenia observed likely would prevent further dose escalation of ifosfamide or addition of other myelosuppressive agents without additional means of bone marrow support in this population of patients.
16例在接受放疗及含亚硝基脲类化疗后出现CT或MRI扫描证实为复发性弥漫性星形细胞瘤的患者接受了异环磷酰胺(2500mg/m²/天,连续3天)和美司钠(500mg/m²/剂,每天5剂,连续3天)治疗。毒性主要表现为白细胞减少,60%的患者白细胞最低点低于1500/μL。3例患者出现过度嗜睡,其中1例可能导致了致命性肺炎,但另外2例患者的嗜睡症状可逆转。没有患者有CT或MRI扫描显示肿瘤缩小的证据。1例患者在11.3 +个月时病情稳定,但所有其他患者在开始治疗后不到6个月就出现了疾病进展的证据。肿瘤进展和死亡的中位时间分别为2.0个月和4.8个月。总之,虽然异环磷酰胺和美司钠按此剂量和方案给药是安全的,但没有抗肿瘤效果的证据。在这群患者中,如果没有额外的骨髓支持手段,观察到的白细胞减少程度可能会阻止异环磷酰胺进一步增加剂量或添加其他骨髓抑制药物。