Turkey real-life data: demographic features, treatment results and effects of comorbidities in chronic myeloid leukemia.

International Journal of Hematologic Oncology Pub Date : 2022-06-30 eCollection Date: 2022-06-01 DOI:10.2217/ijh-2021-0008
Guray Saydam, Ali Unal, Ibrahim Celalettin Haznedaroglu, Abdullah Hacihanifioglu, Ozgur Mehtap, Erdal Kurtoglu, Mesut Gocer, Mehmet Turgut, Engin Kelkitli, Memis Hilmi Atay, Nil Guler, Basak Unver Koluman, Mehmet Sonmez, Nergiz Erkut, Emin Kaya, Irfan Kuku, Mehmet Ali Erkurt, Gulsum Ozet, Funda Ceran, Fahri Sahin, Nur Soyer, Meliha Nalcaci, Mehmet Yilmaz, Sirac Bozkurt, Birkan Aver, Begum Ozdengulsun, Egemen Ozbilgili, Osman Ilhan
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Abstract

Aim: This study aimed to identify patient characteristics, treatment patterns and outcomes and to evaluate the effects of presence of comorbidities at diagnosis in chronic phase (CP)-chronic myeloid leukemia (CML) patients in Turkey.

Materials & methods: Hospital records between 2005 and 2018 were retrospectively reviewed.

Results: Of 861 CP-CML patients included, 31% had at least one comorbidity at diagnosis. Sex, cardiovascular disease status at diagnosis and molecular (at least major) and cytogenetic (partial and complete) responses were the independent predictors of survival.

Conclusion: The response rates of CP-CML patients to the tyrosine kinase inhibitors were satisfactory. In addition to tolerability and side effect profiles of drugs, comorbidity status of patients should also be considered in treatment choice in CML patients.

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土耳其现实生活数据:慢性髓性白血病的人口统计学特征、治疗结果和合并症的影响。
目的:本研究旨在确定土耳其慢性期(CP)-慢性髓性白血病(CML)患者的患者特征、治疗模式和结果,并评估诊断时存在合并症的影响。材料与方法:回顾性分析2005 - 2018年的医院记录。结果:在861例CP-CML患者中,31%在诊断时至少有一种合并症。性别、诊断时的心血管疾病状态以及分子(至少主要)和细胞遗传学(部分和完全)反应是生存的独立预测因素。结论:CP-CML患者对酪氨酸激酶抑制剂的有效率令人满意。在CML患者的治疗选择中,除了药物的耐受性和副作用外,还应考虑患者的合并症状况。
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3
审稿时长
13 weeks
期刊介绍: International Journal of Hematologic Oncology welcomes unsolicited article proposals. Email us today to discuss the suitability of your research and our options for authors, including Accelerated Publication. Find out more about publishing open access with us here.
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