Myeloproliferative Neoplasm Symptom Assessment Total Symptom Score (MPN-SAF TSS) in Chronic Myeloproliferative Neoplasms with Relation to Genetic Burden and Thrombosis

IF 1.5 4区 医学 Q3 HEMATOLOGY Turkish Journal of Hematology Pub Date : 2024-08-28 Epub Date: 2024-05-27 DOI:10.4274/tjh.galenos.2024.2024.0011
Elif Gülsüm Ümit, Mehmet Baysal, Hakkı Onur Kırkızlar, Ahmet Muzaffer Demir
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Abstract

The Myeloproliferative Neoplasm Symptom Assessment Total Symptom Score (MPN-SAF TSS) is a surrogate marker for symptom evaluation in chronic myeloproliferative neoplasms (MPNs). However, insufficient data are available regarding the relationship among the MPN-SAF TSS, JAK2 mutation allele burden, and thrombosis. In this retrospective analysis, we aimed to determine the genetic burdens, clinical features, and relationships with MPN-SAF TSS in MPN patients. One hundred thirty JAK2V617F-positive patients with MPNs were included in our study. We calculated the MPN-SAF TSS for all patients and compared it with their clinical characteristics. Patients with higher JAK2V617F mutation allele burden had higher MPN-SAF TSS values (p=0.008). Patients with thrombosis had higher MPN-SAF TSS than patients without thrombosis (p=0.003). The mean MPN-SAF TSS was higher in patients with primary myelofibrosis compared to those with polycythemia vera and essential thrombocythemia. Thrombosis was associated with increased symptom severity in several domains, including fatigue, abdominal discomfort, inactivity, night sweats, pruritus, weight loss, and early satiety. Additionally, an increase in JAK2 allele burden was observed with higher symptom scores. The MPN-SAF TSS proved to be a reliable tool for assessing symptom burden in Turkish MPN patients. Furthermore, the significant association between thrombosis occurrence and symptom severity suggests that thrombotic events may contribute to symptom development. Notably, increasing JAK2 allele burden was correlated with more severe symptoms, highlighting its potential role in predicting disease burden. This study emphasizes the importance of symptom assessment in MPN patients and supports the incorporation of the MPN-SAF TSS in routine clinical practice to enhance patient care and management.

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慢性骨髓增生性肿瘤症状评估总分(MPN-SAF TSS)与遗传负担和血栓形成的关系。
骨髓增殖性肿瘤症状评估总分(MPN-SAF TSS)是慢性骨髓增殖性肿瘤症状评估的替代指标。目前还没有足够的数据显示 MPN-SAF TSS、JAK2 突变等位基因负担和血栓形成之间的关系。在这项回顾性分析中,我们旨在确定 MPN 患者的基因负担、临床特征以及与 MPN-SAF TSS 的关系。我们的研究共纳入了 130 名 JAK2V617F 阳性的 MPN 患者。我们计算了 MPN-SAF TSS,并将其与临床特征进行了比较。JAK2V617F等位基因突变负荷较高的患者的MPN-SAF TSS较高(P值为0,008)。血栓形成患者的 MPN-SAF TSS 评分高于无血栓形成患者(p 值 0.003)。原发性骨髓纤维化(PMF)患者的 MPN-SAF TSS 平均值高于 PV 和 ET 患者。血栓形成与多个领域的症状严重程度增加有关,包括疲劳、腹部不适、不活动、盗汗、瘙痒、体重减轻和早饱。此外,还观察到 JAK2 等位基因负荷的增加与症状评分的升高有关。事实证明,MPN-SAF TSS 是评估土耳其 MPN 患者症状负担的可靠工具。此外,血栓形成与症状严重程度之间存在明显关联,这表明血栓事件可能会导致症状发展。值得注意的是,JAK2等位基因负担的增加与更严重的症状相关,这突显了它在预测疾病负担方面的潜在作用。这项研究强调了对 MPN 患者进行症状评估的重要性,并支持将 MPN-SAF TSS 纳入常规临床实践,以加强对患者的护理和管理。
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来源期刊
CiteScore
2.90
自引率
3.80%
发文量
45
审稿时长
1 months
期刊介绍: The Turkish Journal of Hematology is published quarterly (March, June, September, and December) by the Turkish Society of Hematology. It is an independent, non-profit peer-reviewed international English-language periodical encompassing subjects relevant to hematology. The Editorial Board of The Turkish Journal of Hematology adheres to the principles of the World Association of Medical Editors (WAME), International Council of Medical Journal Editors (ICMJE), Committee on Publication Ethics (COPE), Consolidated Standards of Reporting Trials (CONSORT) and Strengthening the Reporting of Observational Studies in Epidemiology (STROBE). The aim of The Turkish Journal of Hematology is to publish original hematological research of the highest scientific quality and clinical relevance. Additionally, educational material, reviews on basic developments, editorial short notes, images in hematology, and letters from hematology specialists and clinicians covering their experience and comments on hematology and related medical fields as well as social subjects are published. As of December 2015, The Turkish Journal of Hematology does not accept case reports. Important new findings or data about interesting hematological cases may be submitted as a brief report.
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