Ajani J A, Winn R, Baez L, Pollock T, Maher T, Hallinan-Fueger B, Newman J
Department of Gastrointestinal Oncology and Digestive Diseases, University of Texas M.D. Anderson Cancer Center, Houston.
Cancer Invest. 1994;12(5):488-90. doi: 10.3109/07357909409021408.
Merbarone, 5-(N-phenylcarboxamido)-2-thiobarbituric acid (NSC 336628), is a derivative of barbituric acid and represents a unique class of antineoplastic agents. We treated 16 patients with advanced gastric carcinoma in a phase II study of merbarone. All patients were previously untreated with chemotherapy or biological therapy. The starting dose of merbarone was 1000mg/m2 infused over 24 hr for 5 consecutive days every 21 days. A median of two courses (range, 1-7) was given. None of the patients achieved a complete or partial response; however, 3 patients achieved a transient minor response. Toxicity was mild to moderate in most patients, but 1 patient died of treatment-related neutropenia and sepsis. Our data suggest that merbarone at this dose and schedule is inactive against gastric carcinoma. The evidence of minor response suggests that analog research may be worthwhile to pursue.
美巴龙,即5-(N-苯基甲酰胺基)-2-硫代巴比妥酸(NSC 336628),是巴比妥酸的衍生物,代表一类独特的抗肿瘤药物。我们在一项美巴龙的II期研究中治疗了16例晚期胃癌患者。所有患者此前均未接受过化疗或生物治疗。美巴龙的起始剂量为1000mg/m²,每21天连续5天在24小时内输注完毕。中位给予两个疗程(范围为1 - 7个疗程)。没有患者达到完全缓解或部分缓解;然而,有3例患者达到短暂的轻微缓解。大多数患者的毒性为轻度至中度,但有1例患者死于与治疗相关的中性粒细胞减少和败血症。我们的数据表明,该剂量和方案的美巴龙对胃癌无效。轻微缓解的证据表明,类似物研究可能值得继续进行。