Paul T Roshni, Uppin Shantveer G, Uppin Megha S, Jacob Rachel T, Rao D Raghunadha, Rajappa Senthil J
Indian J Hematol Blood Transfus. 2010 Jun;26(2):56-61. doi: 10.1007/s12288-010-0030-6. Epub 2010 Oct 5.
Imatinib Mesylate, a Tyrosine Kinase inhibitor, is presently the drug of choice for Chronic myeloid leukemia (CML). During therapy, a few patients develop myelosuppression and present with cytopenias. To study the bone marrow morphology in imatinib treated CML patients presenting with persistent cytopenias. The cases were retrieved from the Hematopathology record files, Department of Pathology; the study period being January 2008-June 2009. Cases of CML on Imatinib presenting with grade 2 or more anemia, neutropenia and/or thrombocytopenias with bone marrow studies, were included in the study. The morphology of all cases was reviewed with cytogenetic studies. Follow-up details were obtained from the Medical Oncology records. During the study period, 683 Imatinib treated CML patients had bone marrow studies as part of their follow-up investigations. Of these, 60 patients (9%) had some form of persistent cytopenia. The patients ranged from 21 to 75 years of age with a median age of 38 years. The male:female ratio was 1:1. There were 46 patients with ≥grade 2 anemia, 25 patients with ≥grade 2 neutropenia and 37 patients with ≥grade 2 thrombocytopenia. Of these, 18 patients had bicytopenia and 13 cases had pancytopenia. The marrow evaluation revealed morphologic response in 30 patients, persistent marrow disease in five patients, marrow hypoplasia in six patients, extensive stromal changes including fibrosis in five patients, megaloblastic erythropoiesis in 11 patients and disease progression to accelerated or blast crisis in three patients. Various degrees of cytopenias may occur in few patients of CML on imatinib therapy. Regular hematologic follow-up is required so that the drug may be stopped or dose modified as per the individual's needs.
甲磺酸伊马替尼是一种酪氨酸激酶抑制剂,目前是慢性粒细胞白血病(CML)的首选药物。在治疗期间,少数患者会出现骨髓抑制并伴有血细胞减少。为研究接受伊马替尼治疗且伴有持续性血细胞减少的CML患者的骨髓形态。病例取自病理科血液病理学记录档案;研究时间段为2008年1月至2009年6月。纳入研究的病例为接受伊马替尼治疗的CML患者,伴有2级或更严重的贫血、中性粒细胞减少和/或血小板减少,并进行了骨髓检查。所有病例的形态学均结合细胞遗传学研究进行了复查。随访细节从医学肿瘤学记录中获取。在研究期间,683例接受伊马替尼治疗的CML患者进行了骨髓检查作为其随访调查的一部分。其中,60例患者(9%)出现某种形式的持续性血细胞减少。患者年龄在21岁至75岁之间,中位年龄为38岁。男女比例为1:1。有46例患者贫血≥2级,25例患者中性粒细胞减少≥2级,37例患者血小板减少≥2级。其中,18例患者有二系血细胞减少,13例患者有全血细胞减少。骨髓评估显示30例患者有形态学缓解,5例患者有持续性骨髓疾病,6例患者有骨髓增生低下,5例患者有包括纤维化在内的广泛基质改变,11例患者有巨幼细胞性红细胞生成,3例患者疾病进展为加速期或急变期。少数接受伊马替尼治疗的CML患者可能会出现不同程度的血细胞减少。需要定期进行血液学随访,以便根据个体需求停药或调整剂量。