Lotz J P, Grange J D, Hannoun L, Boudghene F, Amiot X, Lamarque D, Andre T, Esteso A, Bellaiche A, Bouleuc C
Service of Clinical Oncology, Hospital Tenon, Paris, France.
Eur J Cancer. 1994;30A(9):1319-25. doi: 10.1016/0959-8049(94)90181-3.
Based on the in vitro and in vivo potentiation of the cytotoxic activity of chemotherapeutic agents by the interferons, a pilot study combining human recombinant alpha-2b interferon (IFN) and doxorubicin was conducted for the treatment of unresectable, histologically proven hepatocellular carcinoma. Between March 1988 and May 1990, 21 patients (median age: 60 years, range: 29-76) entered the study. The dose of doxorubicin was fixed at 35 mg/m2, every 3 weeks. The dose of alpha-2b IFN was 6 million U/m2 per day, 5 days a week. 3 patients (14%) obtained a partial response lasting 11, 16 and 30 months, and 1 had a stable disease during 8 months. The other 17 patients died within a median survival time of 4 months. All patients experienced flu-like symptoms. 7 patients experienced WHO grade III-IV haematological toxicity. We conclude that the association of alpha-2b IFN and doxorubicin is feasible, with respect to the use of doxorubicin at an inferior dose level than the same agent used without IFN. The response rate is comparable to that observed with doxorubicin used alone. Further phase I studies and randomised trials are required to confirm the role of this regimen in the treatment of unresectable hepatocellular carcinoma.
基于干扰素对化疗药物细胞毒性活性的体内外增强作用,开展了一项将重组人α-2b干扰素(IFN)与阿霉素联合应用治疗无法切除的、经组织学证实的肝细胞癌的初步研究。1988年3月至1990年5月期间,21例患者(中位年龄:60岁,范围:29 - 76岁)进入该研究。阿霉素剂量固定为35mg/m²,每3周给药一次。α-2b干扰素剂量为每日600万U/m²,每周给药5天。3例患者(14%)获得了持续11、16和30个月的部分缓解,1例患者病情稳定8个月。其他17例患者在中位生存时间4个月内死亡。所有患者均出现流感样症状。7例患者出现世界卫生组织III - IV级血液学毒性。我们得出结论,α-2b干扰素与阿霉素联合应用是可行的,与未联合干扰素使用时相比,阿霉素使用剂量较低。缓解率与单独使用阿霉素时观察到的缓解率相当。需要进一步开展I期研究和随机试验来证实该方案在治疗无法切除的肝细胞癌中的作用。