Jeremic B, Grujicic D, Jevremovic S, Stanisavljevic B, Milojevic L, Djuric L, Mijatovic L
Department of Oncology, University Hospital, Kragujevac, Yugoslavia.
J Clin Oncol. 1992 Jul;10(7):1074-7. doi: 10.1200/JCO.1992.10.7.1074.
A phase II study that used combination chemotherapy with carboplatin (CBDCA) and etoposide (VP 16) (CE) was performed on patients with recurrent malignant glioma to investigate tumor control and toxicity.
Thirty-eight patients were treated with CBDCA 300 mg/m2 on days 1 to 3 and VP 16 100 mg/m2 on days 1 to 5. A minimum of three courses were required unless the patient had a rapid progression of disease (PD). Courses were repeated every 4 weeks.
We observed partial responses (PRs) in eight of 38 patients (21%), stable disease (SD) in 12 of 38 (32%), whereas 18 of 38 (47%) patients had PD. The median time to tumor progression (TTP) for PR and SD patients was 42.5 weeks, whereas the median survival time (MST) for PR and SD patients was 47.5 weeks. Three groups of toxicities were observed: hematologic, gastrointestinal, and hepatic. No grade 4 Eastern Cooperative Oncology Group toxicity was observed.
This regimen has shown at least comparable results with other series that used platinum-based agents. Further studies that use these agents in various-dose schedules and drug combinations are warranted.
对复发性恶性胶质瘤患者进行一项使用卡铂(CBDCA)和依托泊苷(VP16)联合化疗(CE)的II期研究,以调查肿瘤控制情况和毒性。
38例患者在第1至3天接受卡铂300mg/m²治疗,在第1至5天接受依托泊苷100mg/m²治疗。除非患者疾病快速进展(PD),否则至少需要三个疗程。疗程每4周重复一次。
我们观察到38例患者中有8例(21%)出现部分缓解(PR),38例中有12例(32%)病情稳定(SD),而38例中有18例(47%)患者出现PD。PR和SD患者的肿瘤进展中位时间(TTP)为42.5周,而PR和SD患者的中位生存时间(MST)为47.5周。观察到三组毒性反应:血液学、胃肠道和肝脏毒性。未观察到4级东部肿瘤协作组毒性反应。
该方案已显示出与其他使用铂类药物的系列研究至少相当的结果。有必要进一步研究这些药物的不同剂量方案和药物组合。