Department of Cellular Biotechnologies and Hematology, Sapienza University, Rome, Italy.
Mediterr J Hematol Infect Dis. 2011;3(1):e2011021. doi: 10.4084/MJHID.2011.021. Epub 2011 May 16.
Imatinib has become first line therapy in chronic myeloid leukemia patients. Little is known about the infective consequences during the treatment with this drug in large series of chronic phase patients.
From January 2001 to September 2006 we treated with imatinib 250 patients in first line (early CP) or after interferon failure (late CP), out of clinical trials and recorded all the bacterial and viral infections occurred.
We recorded a similar incidence of bacterial and viral infections both in first line and late CP patients (respectively, 16% and 13%) during 3.5 years of follow-up. Analysis of presenting features predisposing to infections revealed differences only in late CP patients, with elevated percentage of high Sokal risk patients and a more longer median time from diagnosis to start of imatinib.
Opportunistic infections and reactivation of Herpes Zoster are observed during imatinib therapy at very low incidence.
伊马替尼已成为慢性髓性白血病患者的一线治疗药物。在大规模慢性期患者的研究中,对于该药物治疗期间的感染后果知之甚少。
从 2001 年 1 月至 2006 年 9 月,我们在临床试验之外,用伊马替尼治疗了 250 例一线(早期慢性期)或干扰素治疗失败(晚期慢性期)的患者,并记录了所有发生的细菌和病毒感染。
在 3.5 年的随访中,我们发现一线治疗和晚期慢性期患者的细菌和病毒感染发生率相似(分别为 16%和 13%)。对易感染的特征进行分析发现,只有晚期慢性期患者存在差异,高危索卡尔风险患者的比例升高,从诊断到开始使用伊马替尼的中位时间更长。
在伊马替尼治疗期间,机会性感染和带状疱疹的再激活发生率非常低。