Quagliana J M, O'Bryan R M, Baker L, Gottlieb J, Morrison F S, Eyre H J, Tucker W G, Costanzi J
Cancer Treat Rep. 1977 Jan-Feb;61(1):51-4.
A phase II study utilizing 5-azacytidine in the treatment of patients with solid tumors was carried out by the Southwest Oncology Group (SWOG-7208). Of 214 patients entered in the study 191 were eligible and 167 were evaluable. While initially they received 225 mg/m2 iv on Days 1--5 every 3 weeks because of toxicity the dose was subsequently reduced to 175mg/m2 and later to 150 mg/m2. Five partial regressions, 2.6% of the eligible patients and 3% of the evaluable patients, lasting from 28 to 77 days were observed. Sixteen patients 8.4% of the eligible patients and 9.6% of the evaluable patients, had no significant change in their disease for 39--255 days. The major toxicities were myelosuppressive and gastrointestinal with 13 deaths attributable to drug toxicity: 11 due to sepsis and two due to cerebral hemorrhage. 5-Azacytidine induced few favorable responses; those that did occur usually were of poor quality and short duration and were associated with significant toxicity.
西南肿瘤协作组(SWOG - 7208)开展了一项利用5 - 氮杂胞苷治疗实体瘤患者的II期研究。在参与该研究的214例患者中,191例符合条件,167例可进行评估。由于毒性,最初他们每3周在第1 - 5天接受225 mg/m²静脉注射,随后剂量降至175mg/m²,之后又降至150 mg/m²。观察到5例部分缓解,占符合条件患者的2.6%,可评估患者的3%,缓解持续时间为28至77天。16例患者(占符合条件患者的8.4%,可评估患者的9.6%)疾病在39 - 255天内无显著变化。主要毒性为骨髓抑制和胃肠道毒性,13例死亡归因于药物毒性:11例死于败血症,2例死于脑出血。5 - 氮杂胞苷诱导的有效反应较少;确实出现的那些反应通常质量较差且持续时间短,并伴有显著毒性。