Nielsen B, Braide I
University Department of Medicine and Haematology, County Hospital, Aarhus, Denmark.
Eur J Haematol. 1992 Oct;49(4):174-9. doi: 10.1111/j.1600-0609.1992.tb00044.x.
Thirty-six HCL patients were treated with 2 x 10(6) U/m2 IFN-alpha-2b three times weekly for 24 months, followed by 12 months of treatment with one of three doses ranging from 0.5 x 10(6) U to 2 x 10(6) U/m2. For most patients the response continued to improve during the whole treatment period, and there were no cases of disease progression during treatment. Patients with disease of short duration before IFN treatment and/or non-splenectomized patients seemed to respond more slowly than others, but there were no differences between patients treated with the different IFN doses. Toxicity was usually WHO grade 1 or 2. The continued improvement in a large number of patients even with very small IFN doses might indicate that only a small number of true complete responses are reached after 24 months of treatment, thus explaining the reported high relapse rate after early discontinuation of treatment. It therefore seems worthwhile--also from a cost/benefit point of view--to test long-term or continuous IFN-alpha treatment at other centres.
36例毛细胞白血病(HCL)患者接受2×10⁶ U/m²干扰素α-2b治疗,每周3次,共24个月,随后用0.5×10⁶ U至2×10⁶ U/m²三种剂量之一进行12个月的治疗。对于大多数患者,在整个治疗期间反应持续改善,治疗期间无疾病进展病例。干扰素治疗前病程短的患者和/或未行脾切除术的患者似乎比其他患者反应更慢,但不同干扰素剂量治疗的患者之间无差异。毒性通常为世界卫生组织1级或2级。即使使用非常小的干扰素剂量,大量患者仍持续改善,这可能表明治疗24个月后仅达到少数真正的完全缓解,从而解释了早期停药后报道的高复发率。因此,从成本效益的角度来看,在其他中心测试长期或持续的干扰素α治疗似乎是值得的。