Silver R T
Section of Oncology, Cornell University Medical College, New York, NY.
Semin Hematol. 1990 Jul;27(3 Suppl 4):6-14.
Interferon alfa has been used in the treatment of myeloproliferative disorders, particularly chronic myeloid leukemia, polycythemia vera, and idiopathic thrombocythemia. The effectiveness of interferon alfa in agnogenic myeloid metaplasia needs additional evaluation, although preliminary evidence suggests that it may be more efficacious when used in the cellular (ie, proliferative) phase than when the marrow is fibrotic or osteosclerotic. Cytogenetic and molecular changes after interferon alfa therapy are apparent in patients with chronic myeloid leukemia, as manifested by change in the Philadelphia chromosome and BCR-ABL gene, respectively. The exact role of interferon in prolonging the life of chronic myeloid leukemia patients, however, remains to be determined in larger studies of longer duration. Interferon treatment seems to be well tolerated, and the frequency of treatment-limiting toxicity is low. Data to date suggest that interferon alfa may be a new and effective drug for the treatment of the myeloproliferative disorders.
干扰素α已被用于治疗骨髓增殖性疾病,尤其是慢性髓性白血病、真性红细胞增多症和特发性血小板增多症。尽管初步证据表明,在细胞期(即增殖期)使用时,干扰素α对原发性骨髓化生可能比在骨髓纤维化或骨硬化时更有效,但仍需进一步评估其有效性。在慢性髓性白血病患者中,干扰素α治疗后细胞遗传学和分子变化明显,分别表现为费城染色体和BCR-ABL基因的变化。然而,在更长时间的大型研究中,干扰素在延长慢性髓性白血病患者生命的确切作用仍有待确定。干扰素治疗似乎耐受性良好,治疗限制性毒性的发生率较低。迄今为止的数据表明,干扰素α可能是治疗骨髓增殖性疾病的一种新型有效药物。