Gasparini G, Dal Fior S, Pozza F, Panizzoni G A, Favretto S, Von Hoff D D
St. Bortolo Hospital Vicenza, Italy.
Invest New Drugs. 1991 Aug;9(3):245-52. doi: 10.1007/BF00176977.
In vitro and preclinical in vivo data have shown a synergistic antitumor activity between alpha-interferon and some antiproliferative agents. A phase I study of the concurrent administration of interferon-alpha 2 and mitoxantrone was initiated, to determine the maximum tolerated dose of mitoxantrone given i.v. every 3 weeks in escalating doses combined with a fixed dose of s.c. interferon alpha 2 (6 x 10(6) IU three times per week 3), in patients with advanced solid tumors resistant to conventional chemotherapy. At least three evaluable patients were entered in each dose level of mitoxantrone starting at 4 mg/m2, with no escalations allowed in the same patient. Twenty-seven patients received a total of 101 cycles and five dose-levels were explored (4-6-8-10-12 mg/m2 of mitoxantrone). The dose-limiting toxicities were leukopenia and granulocytopenia at 12 mg/m2 of mitoxantrone, at which dose hematological toxicity occurred in greater than 50% of cases, with one patient presenting grade 4 leuko-granulocytopenia. No severe thrombocytopenia occurred. In the majority of patients transient hepatic enzyme elevations and a flu-like syndrome due to interferon alpha 2 were observed in all dose-levels explored. These observations suggest that the hepatotoxic effects of interferon alpha 2 do not emphasize mitoxantrone side-effects if given simultaneously. When mitoxantrone is administered with 6 x 10(6) IU of interferon alpha 2, the recommended dose for future phase II studies is 10 mg/m2/weeks 3 with escalation up to 12 mg/m2 in selected patients if such a combination is well tolerated in terms of myelosuppression. Regarding therapeutic activity, four out of 25 (16%) cases evaluable for response achieved a partial response.(ABSTRACT TRUNCATED AT 250 WORDS)
体外和临床前体内数据显示,α干扰素与某些抗增殖药物之间具有协同抗肿瘤活性。开展了一项关于同时给予α干扰素2和米托蒽醌的I期研究,以确定在晚期实体瘤患者中,每3周静脉注射递增剂量米托蒽醌与固定剂量皮下注射α干扰素2(每周3次,每次6×10⁶IU)联合使用时米托蒽醌的最大耐受剂量。这些患者对传统化疗耐药。米托蒽醌的每个剂量水平(从4mg/m²开始)至少纳入3名可评估患者,同一患者不允许剂量递增。27名患者共接受了101个周期的治疗,探索了5个剂量水平(米托蒽醌4 - 6 - 8 - 10 - 12mg/m²)。剂量限制性毒性为米托蒽醌12mg/m²时的白细胞减少和粒细胞减少,该剂量下超过50%的病例出现血液学毒性,1例患者出现4级白细胞粒细胞减少。未发生严重血小板减少。在所有探索的剂量水平中,大多数患者观察到因α干扰素2导致的短暂肝酶升高和类似流感的综合征。这些观察结果表明,同时给予α干扰素2时,其肝毒性作用不会加重米托蒽醌的副作用。当米托蒽醌与6×10⁶IU的α干扰素2联合使用时,如果这种联合在骨髓抑制方面耐受性良好,对于未来II期研究,推荐剂量为10mg/m²/3周,在选定患者中可增至12mg/m²。关于治疗活性,25例可评估反应的病例中有4例(16%)获得部分缓解。(摘要截断于250字)