Comorbidities and outcomes of patients with chronic myeloid leukemia treated with tyrosine kinase inhibitors: a real-world, nationwide, retrospective study from Hungary.

IF 2.3 4区 医学 Q3 ONCOLOGY Pathology & Oncology Research Pub Date : 2024-02-20 eCollection Date: 2024-01-01 DOI:10.3389/pore.2024.1611497
Peter Batar, Hussain Alizadeh, Gyorgy Rokszin, Zsolt Abonyi-Toth, Judit Demeter
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Abstract

Purpose: This study aimed to provide real-world evidence on the characteristics, treatment patterns, and outcomes of patients with chronic myeloid leukemia (CML) receiving tyrosine kinase inhibitor (TKI) treatment in Hungary between 2011 and 2019. Patients and methods: This nationwide, retrospective study included patients who were newly diagnosed with CML in Hungarian clinical practice between January 2011 and December 2019. The analysis was based on the reimbursed prescription claims for imatinib, bosutinib, dasatinib, nilotinib, or ponatinib with the ICD-10 code C9210 in a public pharmacy between January 2009 and December 2019 using data from the National Health Insurance Fund (NHIF) of Hungary. CML incidence and prevalence, TKI treatment patterns, comorbidities, and overall survival (OS) were examined. Results: Between 2011 and 2019, altogether 1,407 patients were diagnosed with CML, with an annual average of 156 patients. The number of patients newly initiating first-line TKI therapy for CML significantly increased between 2011 and 2019 (2011: n = 136 vs. 2019: n = 191; p = 0.0043). Nilotinib was typically prescribed for younger patients (≤64 years), while older patients (≥65 years) mostly received imatinib. The most common comorbidity of CML patients was hypertension, and the proportion of patients with other malignancies was relatively high in all treatment groups. 5-year OS was 77.1% during the whole study period. Patients initiating first-line TKI treatment for CML in 2015 had significantly better 4-year OS compared to those starting treatment in 2011 (82.4% vs. 73.5%, respectively, (HR 0.53 (95%CI 0.32-0.87) p = 0.0118). Conclusion: This study is the first to provide insights into the characteristics, treatment patterns, and outcomes of CML patients treated with TKIs in Hungarian clinical practice between 2011 and 2019. We found slightly lower OS rates compared to other European countries, however, there was a statistically significant improvement in 4-year OS during the study period. The management of CML was in line with international guidelines and recommendations.

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接受酪氨酸激酶抑制剂治疗的慢性髓性白血病患者的并发症和预后:来自匈牙利的一项真实世界、全国范围的回顾性研究。
目的:本研究旨在提供2011年至2019年期间匈牙利接受酪氨酸激酶抑制剂(TKI)治疗的慢性髓性白血病(CML)患者的特征、治疗模式和预后的真实证据。患者和方法:这项全国性的回顾性研究纳入了 2011 年 1 月至 2019 年 12 月期间在匈牙利临床实践中新诊断出的 CML 患者。分析基于 2009 年 1 月至 2019 年 12 月期间公共药房中 ICD-10 编码为 C9210 的伊马替尼、博苏替尼、达沙替尼、尼洛替尼或泊纳替尼的报销处方申请,数据来自匈牙利国家医疗保险基金(NHIF)。对 CML 发病率和流行率、TKI 治疗模式、合并症和总生存期(OS)进行了研究。研究结果2011年至2019年期间,共有1407名患者被确诊为CML,年均156人。2011年至2019年期间,新开始一线TKI治疗的CML患者人数显著增加(2011年:n = 136 vs. 2019年:n = 191; p = 0.0043)。尼罗替尼通常用于年轻患者(≤64 岁),而老年患者(≥65 岁)大多接受伊马替尼治疗。CML患者最常见的合并症是高血压,在所有治疗组中,患有其他恶性肿瘤的患者比例相对较高。在整个研究期间,5年生存率为77.1%。与2011年开始治疗的患者相比,2015年开始一线TKI治疗的CML患者的4年OS明显更好(分别为82.4%对73.5%,HR 0.53 (95%CI 0.32-0.87) p = 0.0118)。结论这项研究首次深入探讨了2011年至2019年期间在匈牙利临床实践中接受TKIs治疗的CML患者的特征、治疗模式和预后。我们发现,与其他欧洲国家相比,OS 率略低,但在研究期间,4 年 OS 有了统计学意义上的显著改善。CML的管理符合国际指南和建议。
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
134
审稿时长
4-8 weeks
期刊介绍: Pathology & Oncology Research (POR) is an interdisciplinary Journal at the interface of pathology and oncology including the preclinical and translational research, diagnostics and therapy. Furthermore, POR is an international forum for the rapid communication of reviews, original research, critical and topical reports with excellence and novelty. Published quarterly, POR is dedicated to keeping scientists informed of developments on the selected biomedical fields bridging the gap between basic research and clinical medicine. It is a special aim for POR to promote pathological and oncological publishing activity of colleagues in the Central and East European region. The journal will be of interest to pathologists, and a broad range of experimental and clinical oncologists, and related experts. POR is supported by an acknowledged international advisory board and the Arányi Fundation for modern pathology.
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