Yung W K, Mechtler L, Gleason M J
Department of Neuro-Oncology, University of Texas MD Anderson Cancer Center, Houston 77030.
J Clin Oncol. 1991 May;9(5):860-4. doi: 10.1200/JCO.1991.9.5.860.
Thirty patients with recurrent malignant glioma were treated with intravenous (IV) carboplatin (CBDCA) every 4 weeks at a starting dose of 400 mg/m2 escalating to 450 mg/m2. All patients had documented recurrent tumor after prior radiotherapy but had not received prior chemotherapy. Of 29 assessable patients, four (14%) responded to the treatment for 44, 51+, 72, and 91 weeks; 10 (34%) achieved stable disease (S); while 15 (52%) had progressive disease (P). The total response (responses plus S) rate was 48%, with a median time to progression (MTP) of 26 weeks in these patients; the MTP for all 29 patients was 11 weeks. The toxic effects were mainly hematologic, with thrombocytopenia and granulocytopenia being mild at 400 mg/m2 and 450 mg/m2 doses. NO neurotoxicity or renal toxicity was encountered. These results suggest that CBCDA given at 400 mg/m2 or 450 mg/m2 every 4 weeks is marginally active in patients with recurrent malignant gliomas. Since hematologic toxicity is mild, a higher dose could possibly be given, and may increase the response rate.
30例复发性恶性胶质瘤患者接受静脉注射卡铂(CBDCA)治疗,每4周一次,起始剂量为400mg/m²,逐渐增至450mg/m²。所有患者在先前接受放疗后均有复发性肿瘤记录,但未接受过先前的化疗。在29例可评估患者中,4例(14%)对治疗有反应,持续时间分别为44周、51 +周、72周和91周;10例(34%)病情稳定(S);15例(52%)病情进展(P)。总缓解率(反应加病情稳定)为48%,这些患者的中位疾病进展时间(MTP)为26周;所有29例患者的MTP为11周。毒性作用主要为血液学方面,在400mg/m²和450mg/m²剂量时,血小板减少和粒细胞减少较轻。未发现神经毒性或肾毒性。这些结果表明,每4周给予400mg/m²或450mg/m²的CBDCA对复发性恶性胶质瘤患者有一定活性。由于血液学毒性较轻,可能给予更高剂量,这可能会提高缓解率。