Evaluation of Clinical Outcomes and Treatment Complications in Hairy Cell Leukemia: A Single-Center Retrospective Analysis

IF 1.9 Q4 ONCOLOGY
Cancer reports Pub Date : 2025-10-01 DOI:10.1002/cnr2.70356
M. Garcia Fasanella, A. Mozos, J. Briones, J. F. Nomdedeu, S. Novelli
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Abstract

Background

Hairy cell leukemia (HCL) is a rare disorder characterized by splenomegaly, pancytopenia, and proliferation with “hairy” lymphocytes. Treatment is based on purine analogs and anti-CD20 antibodies, often resulting in significant adverse effects.

Aims

The objective of this study is to describe the frequency, clinical, and biological characteristics of a historic cohort of HCL patients in our center and the most common side effects related to treatment with purine analogs.

Methods and Results

This study analyzed 21 patients treated between 2009 and 2023, focusing on clinical characteristics, treatment response, complications, and survival outcomes. Cladribine treatment achieved complete response in 77.8% of patients. The 5-year OS and PFS were 100% and 91.7%, respectively. Infections, pathogens such as herpes viruses and mycobacteria, were major complications, impacting 38% of patients. Severe skin reactions were noted in patients treated with cladribine.

Conclusion

The study highlights cladribine's effectiveness in inducing remission in HCL patients, pointing out the significant risks of infections and other adverse effects. Introducing targeted treatments like BRAF inhibitors provides promising alternatives, especially for resistant patients or those intolerant to purine analogs. Future strategies should focus on integrating targeted therapies to reduce treatment-related morbidity.

Abstract Image

毛细胞白血病的临床结局和治疗并发症的评价:单中心回顾性分析
毛细胞白血病(HCL)是一种罕见的疾病,其特征是脾肿大、全血细胞减少和“毛状”淋巴细胞增生。治疗是基于嘌呤类似物和抗cd20抗体,往往导致显著的不良反应。本研究的目的是描述我们中心历史队列HCL患者的频率、临床和生物学特征,以及与嘌呤类似物治疗相关的最常见副作用。方法与结果本研究分析了2009 - 2023年间治疗的21例患者的临床特征、治疗反应、并发症和生存结局。77.8%的患者通过克拉德滨治疗获得完全缓解。5年OS为100%,PFS为91.7%。感染,病原体如疱疹病毒和分枝杆菌,是主要的并发症,影响了38%的患者。使用克拉宾治疗的患者出现严重的皮肤反应。结论本研究强调了克拉德滨在HCL患者中诱导缓解的有效性,指出了感染和其他不良反应的显著风险。引入BRAF抑制剂等靶向治疗提供了有希望的替代方案,特别是对于耐药患者或对嘌呤类似物不耐受的患者。未来的战略应侧重于整合靶向治疗,以减少治疗相关的发病率。
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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来源期刊
Cancer reports
Cancer reports Medicine-Oncology
CiteScore
2.70
自引率
5.90%
发文量
160
审稿时长
17 weeks
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