Heideman R L, Kovnar E H, Kellie S J, Douglass E C, Gajjar A J, Walter A W, Langston J A, Jenkins J J, Li Y, Greenwald C
Department of Hematology-Oncology, St Jude Childrens Research Hospital, Memphis, TN 38101, USA.
J Clin Oncol. 1995 Sep;13(9):2247-54. doi: 10.1200/JCO.1995.13.9.2247.
We evaluated the clinical efficacy of preirradiation carboplatin (CARBO) and etoposide (VP-16) in 25 patients with newly diagnosed embryonal CNS tumors.
Sixteen patients with high-risk medulloblastoma and nine with other embryonal tumors were treated with two daily doses of CARBO 350 mg/m2 and VP-16 100 mg/m2 (CARBO/VP) every 21 days for four cycles before standard craniospinal irradiation. Patients with disease progression (PD) before radiation therapy were additionally treated with intensive postirradiation cyclophosphamide (CYCLO) and vincristine (VINC).
Among 23 assessable patients, 48% (95% confidence interval, 27% to 69%) had a complete response (CR) or partial response (PR) to CARBO/VP; eight had PD. Among the subgroup of 15 assessable patients with medulloblastoma, 53% had a CR or PR (95% confidence interval, 27% to 79%) and five PD. The toxicity of CARBO/VP was predominantly hematologic; although grade IV neutropenia was common, only five episodes of febrile neutropenia occurred. Only thrombocytopenia was a more common toxicity than in other reported chemotherapy regimens; ototoxicity was less common than in cisplatin (CDDP) regimens.
The responses and survival associated with neoadjuvant CARBO/VP are similar to those with CDDP-containing and other neoadjuvant drug regimens. Although the rate of progression with this regimen may be higher than with similar CDDP-containing regimens, the numbers of patients in other published studies of these agents are too small to detect meaningful statistical differences. Future studies must balance the apparently comparable efficacy of CARBO and CDDP with their differing toxicities.
我们评估了放疗前使用卡铂(CARBO)和依托泊苷(VP - 16)对25例新诊断的胚胎性中枢神经系统肿瘤患者的临床疗效。
16例高危髓母细胞瘤患者和9例其他胚胎性肿瘤患者,在标准的全脑全脊髓放疗前,每21天接受每日两次剂量的CARBO 350 mg/m²和VP - 16 100 mg/m²(CARBO/VP)治疗,共四个周期。放疗前疾病进展(PD)的患者额外接受强化的放疗后环磷酰胺(CYCLO)和长春新碱(VINC)治疗。
在23例可评估患者中,48%(95%置信区间,27%至69%)对CARBO/VP有完全缓解(CR)或部分缓解(PR);8例有疾病进展。在15例可评估的髓母细胞瘤患者亚组中,53%有CR或PR(95%置信区间,27%至79%),5例有疾病进展。CARBO/VP的毒性主要是血液学方面的;虽然IV级中性粒细胞减少很常见,但仅发生了5次发热性中性粒细胞减少事件。只有血小板减少是比其他报道的化疗方案更常见的毒性;耳毒性比顺铂(CDDP)方案少见。
新辅助CARBO/VP治疗的缓解情况和生存率与含CDDP及其他新辅助药物方案相似。虽然该方案的疾病进展率可能高于含类似CDDP的方案,但其他已发表的这些药物研究中的患者数量太少,无法检测到有意义的统计学差异。未来的研究必须在CARBO和CDDP明显相当的疗效与其不同的毒性之间进行权衡。