t细胞大颗粒淋巴细胞白血病的流行病学、生存率和第二原发恶性肿瘤

EJHaem Pub Date : 2025-05-06 DOI:10.1002/jha2.70036
Arya Mariam Roy, Sawyer Bawek, Richa Parikh, Muhammad Salman Faisal, Paola Ghione
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引用次数: 0

摘要

大颗粒淋巴细胞白血病(LGL)是一种罕见的淋巴细胞增生性疾病,关于T-LGL中继发性原发性恶性肿瘤(SPMs)的流行病学、生存和发展的文献有限。方法采用监测、流行病学和最终结果(SEER) 17注册表对2000年至2019年诊断的所有T-LGL病例进行识别,并对原发性T-LGL患者进行分析。与一般人群相比,原发性T-LGL患者的SPMs发病率更高,在T-LGL诊断后的前10年内出现血液恶性肿瘤的风险增加,10年后出现实体瘤的风险增加。结论原发性T-LGL患者有较高的SPMs发生率。需要进一步的研究来更好地了解这种风险增加的原因。试验注册作者已确认该提交不需要临床试验注册
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Epidemiology, Survival, and Second Primary Malignancies in T-Cell Large Granular Lymphocytic Leukemia

Epidemiology, Survival, and Second Primary Malignancies in T-Cell Large Granular Lymphocytic Leukemia

Introduction

Large granular lymphocytic leukemia (LGL) is a rare lymphoproliferative disorder, with limited literature available about the epidemiology, survival, and development of secondary primary malignancies (SPMs) in T-LGL.

Methods

The Surveillance, Epidemiology, and End Results (SEER) 17 registry was used to identify all cases of T-LGL diagnosed between 2000 and 2019, and patients with primary T-LGL were analyzed.

Results

Patients with primary T-LGL were found to have a higher incidence of SPMs compared to the general population, with increased risk for hematological malignancies seen within the first 10 years and solid tumors seen after 10 years of T-LGL diagnosis.

Conclusion

Patients with primary T-LGL were found to have a higher incidence of SPMs. Further research is needed to better understand the reason for this increased risk.

Trial Registration

The authors have confirmed clinical trial registration is not needed for this submission

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