Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.
Department of Medical Science and Division of Hematology, University Hospital, Uppsala, Sweden.
Leukemia. 2016 Jul;30(7):1562-7. doi: 10.1038/leu.2016.59. Epub 2016 Mar 8.
We recently reported an increased incidence of second malignancies in chronic myeloid leukemia (CML) patients treated with tyrosine kinase inhibitors (TKI). To elucidate whether this increase may be linked, not to TKI but rather to a hereditary or acquired susceptibility to develop cancer, we estimated the prevalence of malignancies, autoimmune disease (AD) and chronic inflammatory disease (CID) in CML patients prior to their CML diagnosis. Nationwide population-based registers were used to identify patients diagnosed with CML in Sweden 2002-2012 and to estimate the prevalence of other malignancies, AD and CID prior to their CML diagnosis. For each patient with CML, five matched controls were selected from the general population. Conditional logistic regression was used to calculate odds ratios (OR). Nine hundred and eighty-four CML patients were assessed, representing more than 45 000 person-years of follow-up. Compared with matched controls, the prevalence of prior malignancies and AD was elevated in CML patients: OR 1.47 (95% confidence interval (CI) 1.20-1.82) and 1.55 (95% CI 1.21-1.98), respectively. No associations were detected between CML and previous CID. An increased prevalence of other malignancies and AD prior to the diagnosis of CML suggest that a hereditary or acquired predisposition to cancer and/or autoimmunity is involved in the pathogenesis of CML.
我们最近报道了接受酪氨酸激酶抑制剂 (TKI) 治疗的慢性髓性白血病 (CML) 患者第二恶性肿瘤发病率增加。为了阐明这种增加是否可能与 TKI 无关,而是与癌症发生的遗传或获得性易感性有关,我们在 CML 诊断之前估计了 CML 患者的恶性肿瘤、自身免疫性疾病 (AD) 和慢性炎症性疾病 (CID) 的患病率。全国性基于人群的登记处用于在瑞典 2002-2012 年间识别出被诊断为 CML 的患者,并估计在 CML 诊断之前其他恶性肿瘤、AD 和 CID 的患病率。对于每一位 CML 患者,从普通人群中选择了 5 名匹配的对照者。使用条件逻辑回归计算比值比 (OR)。评估了 984 例 CML 患者,代表超过 45000 人年的随访。与匹配的对照者相比,CML 患者先前恶性肿瘤和 AD 的患病率升高:OR 分别为 1.47(95%置信区间 (CI) 1.20-1.82)和 1.55(95%CI 1.21-1.98)。在 CML 和先前 CID 之间未检测到关联。在 CML 诊断之前,其他恶性肿瘤和 AD 的患病率增加表明,癌症和/或自身免疫的遗传或获得性易感性与 CML 的发病机制有关。