Differences In Hematology And Bcr-Abl Molecular Profiles In Patients With Chronic Myeloid Leukemia Undergoing Tyrosine Kinase Inhibitor Therapy

B. Santosa, Muhammad Ihza Lisan Shidqi, Muhamad Muslim, Haitami Haitami
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Abstract

Chronic myeloid leukemia (CML) is a myeloproliferative malignancy due to the formation of the BCR-ABL fusion gene in chronic myeloid leukemia. This condition causes excessive cell proliferation, resulting in an increase in the number of leukocytes. Tyrosine Kinase Inhibitor (TKI) is a first-line therapy that helps reduce  the percentage of the BCR-ABL fusion gene in patients with chronic myeloid leukemia. This study was conducted to determine differences in the hematological profiles (hemoglobin levels, leukocyte counts, platelet counts) and molecular BCR-ABL in patients with chronic myeloid leukemia before and after 12 months of tyrosine kinase inhibitors therapy. This analytic observational study was administered using a cross-sectional design to in analyzing the medical records of CML patients who underwent TKI therapy at the Sub Specialist Polyclinic of Internal Medicine Hematology Oncology Ulin Banjarmasin Regional Hospital from March 2021-April 2022. Dependent T-test and McNemar's test were performed in data analysis which results showed that 12 month tyrosine kinase inhibitor therapy could increase the hemoglobin levels, decrease leukocyte counts, platelet counts as well as decreasing the percentage of BCR-ABL gene fusion in patients with chronic myeloid leukemia. In conclusion, significant differences were found in the hematological profiles (p<0.001) and the molecular BCR-ABL (p<0.001) before and after 12 months of tyrosine kinase inhibitor therapy  
接受酪氨酸激酶抑制剂治疗的慢性粒细胞白血病患者血液学和Bcr-Abl分子谱的差异
慢性髓性白血病(Chronic myeloid leukemia, CML)是一种骨髓增殖性恶性肿瘤,是由于慢性髓性白血病中BCR-ABL融合基因的形成所致。这种情况会导致细胞过度增殖,导致白细胞数量增加。酪氨酸激酶抑制剂(TKI)是一种一线治疗,有助于降低慢性髓性白血病患者BCR-ABL融合基因的百分比。本研究旨在确定慢性髓性白血病患者在酪氨酸激酶抑制剂治疗前后12个月的血液学特征(血红蛋白水平、白细胞计数、血小板计数)和分子BCR-ABL的差异。本分析性观察性研究采用横断面设计,对2021年3月至2022年4月期间在乌林班贾尔马辛地区医院内科血液学肿瘤科专科综合诊所接受TKI治疗的CML患者的病历进行分析。数据分析采用依赖t检验和McNemar检验,结果显示12个月酪氨酸激酶抑制剂治疗可提高慢性髓系白血病患者血红蛋白水平,降低白细胞计数、血小板计数,降低BCR-ABL基因融合百分率。综上所述,在酪氨酸激酶抑制剂治疗前后12个月的血液学特征(p<0.001)和分子BCR-ABL (p<0.001)存在显著差异
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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