Casato M, Pucillo L P, Leoni M, di Lullo L, Gabrielli A, Sansonno D, Dammacco F, Danieli G, Bonomo L
Department of Clinical Medicine, University of Rome La Sapienza, Italy.
Am J Med. 1995 Oct;99(4):386-91. doi: 10.1016/s0002-9343(99)80186-7.
The purpose of this study was to assess whether granulocytopenia observed in 3 of 38 patients with essential mixed cryoglobulinemia who were treated with low-dose interferon was due to the underlying disease or to synergistic toxicity of interferon with other drugs.
Adverse effects of interferon therapy were monitored in 38 patients affected with type II essential mixed cryoglobulinemia. Patients were treated with 3 million units (MU), daily or on alternate days, of recombinant interferon-alpha 2a (35 patients) or with natural interferon-beta (3 patients). The duration of treatment ranged between 6 and 15 months; the total duration of follow-up, including after therapy, ranged between 8 and 93 months.
None of 35 patients treated with interferon alone developed significant hematologic alterations. In addition, none of 7 patients treated with angiotensin-converting enzyme (ACE) inhibitors alone showed hematologic toxicity. Three patients who were treated with a combination of interferon and ACE inhibitors developed severe granulocytopenia a few days after starting treatment. Granulocytopenia subsided within 1 to 2 weeks after suspending therapy. Resumption of treatment with this drug combination produced a granulocytopenia relapse in 1 patient. In these 3 patients, interferon treatment alone, or ACE inhibitor monotherapy, was not followed by granulocytopenia.
Although severe hematologic toxicity rarely develops in patients treated with low-dose interferon, granulocytopenia occurred in all 3 of our patients with mixed cryoglobulinemia who were treated with a combination of low-dose interferon-alpha 2a and ACE inhibitors. Neither drug alone was toxic in any of our cryoglobulinemic patients, indicating a high risk of severe hematologic toxicity for this drug combination, at least in patients with this disease. Physicians should be aware of this danger when using interferon treatment in patients with this, or possibly other, disorder(s) that also require antihypertensive therapy.
本研究旨在评估38例接受低剂量干扰素治疗的原发性混合性冷球蛋白血症患者中,3例出现的粒细胞减少是由基础疾病所致,还是干扰素与其他药物的协同毒性作用引起。
对38例II型原发性混合性冷球蛋白血症患者的干扰素治疗不良反应进行监测。患者接受300万单位(MU)重组干扰素α-2a(35例患者)每日或隔日治疗,或天然干扰素β(3例患者)治疗。治疗持续时间为6至15个月;随访总持续时间,包括治疗后,为8至93个月。
35例单独接受干扰素治疗的患者均未出现明显的血液学改变。此外,7例单独接受血管紧张素转换酶(ACE)抑制剂治疗的患者均未表现出血液学毒性。3例接受干扰素与ACE抑制剂联合治疗的患者在开始治疗几天后出现严重粒细胞减少。粒细胞减少在暂停治疗后1至2周内消退。恢复使用该药物组合治疗导致1例患者粒细胞减少复发。在这3例患者中,单独使用干扰素治疗或ACE抑制剂单药治疗均未出现粒细胞减少。
尽管低剂量干扰素治疗的患者很少发生严重血液学毒性,但我们3例接受低剂量干扰素α-2a与ACE抑制剂联合治疗的混合性冷球蛋白血症患者均出现了粒细胞减少。单独使用这两种药物对我们的任何冷球蛋白血症患者均无毒性,表明该药物组合至少在患有这种疾病的患者中有发生严重血液学毒性的高风险。在对患有这种或可能其他也需要抗高血压治疗的疾病的患者使用干扰素治疗时,医生应意识到这种危险。