Uemura Makiko, Imataki Osamu, Kawachi Yasunori, Kawakami Kimihiro, Hoshijima Yasuo, Matsuoka Akihito, Kadowaki Norimitsu
Division of Hematology, Rheumatology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Kagawa University, Miki-town, Japan.
Division of Hematology and Stem Cell Transplantation, Department of Internal Medicine, Faculty of Medicine, Kagawa University, 1750-1 Ikenobe, Miki-town, Kagawa, 761-0793, Japan.
Int J Hematol. 2016 Nov;104(5):621-627. doi: 10.1007/s12185-016-2074-3. Epub 2016 Aug 4.
Although the Sokal and Hasford scoring systems are well-known prognostic models specific to chronic myeloid leukemia (CML), whether they can effectively predict outcomes in elderly CML patients with comorbidities has not been fully elucidated. We evaluated the association between comorbidity at diagnosis with treatment outcome and survival in chronic phase CML patients. A questionnaire was administered to patients diagnosed with CML between 2001 and 2012 and treated with tyrosine kinase inhibitors (TKIs). The Charlson comorbidity index (CCI) was used to determine concomitant diseases. In total, 79 patients (33 females; median age, 57 years) were enrolled. CCI scores at diagnosis were between 2 and 11. At the last follow-up, 46 patients showed a major molecular response. Complete cytogenetic response was achieved in 73.4 % of the cases 12 months after TKI administration. We observed only five deaths during the 55.5-month median follow-up period. The risk categories (low/intermediate/high) associated with Sokal and Hasford scores were 33/27/7 and 21/43/3, respectively. The 27 cases with a CCI score >3 had significantly poorer survival after diagnosis (52 cases had a CCI score <2). CCI scores were inversely associated to overall survival. Concomitant comorbidity at diagnosis is associated with poor outcome in CML patients treated with TKIs.
尽管索卡尔(Sokal)和哈斯福德(Hasford)评分系统是慢性髓性白血病(CML)特有的著名预后模型,但它们能否有效预测合并症老年CML患者的预后尚未完全阐明。我们评估了慢性期CML患者诊断时的合并症与治疗结果及生存之间的关联。对2001年至2012年间诊断为CML并接受酪氨酸激酶抑制剂(TKIs)治疗的患者进行了问卷调查。采用查尔森合并症指数(CCI)来确定伴随疾病。总共纳入了7名患者(33名女性;中位年龄57岁)。诊断时的CCI评分在2至11之间。在最后一次随访时,46名患者显示出主要分子反应。在给予TKI 12个月后,73.4%的病例实现了完全细胞遗传学反应。在中位随访期55.5个月期间,我们仅观察到5例死亡。与索卡尔和哈斯福德评分相关的风险类别(低/中/高)分别为33/27/7和21/43/3。CCI评分>3的27例患者诊断后的生存率明显较差(52例患者的CCI评分<2)。CCI评分与总生存期呈负相关。诊断时的合并症与接受TKIs治疗的CML患者的不良预后相关。