Oyekunle Anthony A, Durosinmi Muheez A, Bolarinwa Ramoni A, Owojuyigbe Temilola, Salawu Lateef, Akinola Norah O
Department of Hematology and Immunology, Obafemi Awolowo University, Ile-Ife, Nigeria.; Department of Hematology and Blood Transfusion, Obafemi Awolowo University Teaching Hospitals Complex, Ile-Ife, Nigeria.
Clin Med Insights Blood Disord. 2016 Jun 20;9:9-13. doi: 10.4137/CMBD.S31562. eCollection 2016.
The advent of the tyrosine kinase inhibitors has markedly changed the prognostic outlook for patients with Ph(+) and/or BCR-ABL1 (+) chronic myeloid leukemia (CML). This study was designed to assess the overall survival (OS) of Nigerian patients with CML receiving imatinib therapy and to identify the significant predictors of OS.
All patients with CML receiving imatinib from July 2003 to June 2013 were studied. The clinical and hematological parameters were studied. The Kaplan-Meier technique was used to estimate the OS and median survival. P-value of <0.05 was considered as statistically significant.
The median age of all 527 patients (male/female = 320/207) was 37 (range 10-87) years. There were 472, 47, and 7 in chronic phase (CP), accelerated phase, and blastic phase, respectively. As at June 2013, 442 patients are alive. The median survival was 105.7 months (95% confidence interval [CI], 91.5-119.9); while OS at one, two, and five years were 95%, 90%, and 75%, respectively. Multivariate Cox regression analysis revealed that OS was significantly better in patients diagnosed with CP (P = 0.001, odds ratio = 1.576, 95% CI = 1.205-2.061) or not in patients with anemia (P = 0.031, odds ratio = 1.666, 95% CI = 1.047-2.649). Combining these variables yielded three prognostic groups: CP without anemia, CP with anemia, and non-CP, with significantly different median OS of 123.3, 92.0, and 74.7 months, respectively (χ (2) = 22.042, P = 0.000016).
This study has clearly shown that for Nigerian patients with CML, the clinical phase of the disease at diagnosis and the hematocrit can be used to stratify patients into low, intermediate, and high risk groups.
酪氨酸激酶抑制剂的出现显著改变了费城染色体阳性(Ph(+))和/或BCR-ABL1阳性慢性髓性白血病(CML)患者的预后前景。本研究旨在评估接受伊马替尼治疗的尼日利亚CML患者的总生存期(OS),并确定OS的显著预测因素。
对2003年7月至2013年6月期间所有接受伊马替尼治疗的CML患者进行研究。对临床和血液学参数进行研究。采用Kaplan-Meier技术估计OS和中位生存期。P值<0.05被认为具有统计学意义。
527例患者(男/女=320/207)的中位年龄为37岁(范围10-87岁)。慢性期(CP)、加速期和急变期分别有472例、47例和7例。截至2013年6月,442例患者存活。中位生存期为105.7个月(95%置信区间[CI],91.5-119.9);1年、2年和5年的OS分别为95%、90%和75%。多因素Cox回归分析显示,诊断为CP的患者OS显著更好(P = 0.001,比值比=1.576,95%CI = 1.205-2.061),贫血患者的OS则较差(P = 0.031,比值比=1.666,95%CI = 1.047-2.649)。综合这些变量产生了三个预后组:无贫血的CP、有贫血的CP和非CP,中位OS分别为123.3、92.0和74.7个月,差异有统计学意义(χ(2)=22.042,P = 0.000016)。
本研究清楚地表明,对于尼日利亚CML患者,疾病诊断时的临床分期和血细胞比容可用于将患者分为低、中、高风险组。