McLigeyo Angela, Rajab Jamilla, Ezzi Mohammed, Oyiro Peter, Bett Yatich, Odhiambo Andrew, Ong'ondi Matilda, Mwanzi Sitna, Gatua Mercy, Abinya NAOthieno-
Department of Medicine, Maseno University, Kisumu, Kenya.
Department of Clinical Medicine and Therapeutics, University of Nairobi, Nairobi, Kenya.
Adv Hematol. 2020 May 12;2020:7696204. doi: 10.1155/2020/7696204. eCollection 2020.
Imatinib mesylate is the gold standard for the treatment of all phases of Philadelphia-positive chronic myeloid leukemia. Patients on imatinib treatment may develop cytopenia due to drug toxicity. This study aimed to determine the types, grades, and time course of cytopenia in CML patients on imatinib at a Nairobi hospital.
This was a cross-sectional descriptive study of adult patients aged ≥18 years followed up at the Glivec International Patient Access Program (GIPAP) clinic from 2007 to 2015. Patients who developed cytopenia within 12 months of initiating imatinib were eligible. Clinical and hematologic data were retrieved from the patients' charts and entered into a study proforma. Measures of central tendency such as mean, median, mode, standard deviation, and variance were used for analysis.
Sixty three percent (63.6%) of the 94 patients developed a monocytopenia, with anemia seen in 34%, neutropenia in 27.6%, and thrombocytopenia in 8% of the 94 patients. Anemia plus neutropenia was the most common bicytopenia at 12.7%. Pancytopenia was seen in only 5 of the 94 patients. Most of the cytopenia was grades 2 and 3. Anemia was present at baseline while neutropenia and thrombocytopenia developed within 12 months of imatinib initiation. Anemia resolved during the first 12 months of therapy while neutropenia and thrombocytopenia resolved within 24-36 months of treatment.
Monocytopenia, especially anemia, was the most common type of cytopenia. The cytopenia was predominantly grade 2, developed in majority of the patients within 6 months after imatinib initiation, and had resolved by 24-36 months after imatinib initiation.
甲磺酸伊马替尼是治疗各阶段费城染色体阳性慢性髓性白血病的金标准。接受伊马替尼治疗的患者可能因药物毒性而出现血细胞减少。本研究旨在确定内罗毕一家医院接受伊马替尼治疗的慢性髓性白血病患者血细胞减少的类型、分级及时间进程。
这是一项横断面描述性研究,研究对象为2007年至2015年在格列卫国际患者援助项目(GIPAP)诊所接受随访的≥18岁成年患者。在开始伊马替尼治疗12个月内出现血细胞减少的患者符合条件。从患者病历中检索临床和血液学数据,并录入研究表格。采用均值、中位数、众数、标准差和方差等集中趋势测量指标进行分析。
94例患者中有63.6%出现单核细胞减少,94例患者中34%出现贫血,27.6%出现中性粒细胞减少,8%出现血小板减少。贫血加中性粒细胞减少是最常见的双血细胞减少,发生率为12.7%。94例患者中只有5例出现全血细胞减少。大多数血细胞减少为2级和3级。贫血在基线时就存在,而中性粒细胞减少和血小板减少在开始伊马替尼治疗后12个月内出现。贫血在治疗的前12个月内缓解,而中性粒细胞减少和血小板减少在治疗24 - 36个月内缓解。
单核细胞减少,尤其是贫血,是最常见的血细胞减少类型。血细胞减少主要为2级,大多数患者在开始伊马替尼治疗后6个月内出现,并在开始伊马替尼治疗后24 - 36个月内缓解。