Nodular lymphocyte-predominant Hodgkin lymphoma revisited: current management strategies and future perspectives.

IF 2.2 4区 医学 Q3 HEMATOLOGY Leukemia & Lymphoma Pub Date : 2025-01-02 DOI:10.1080/10428194.2024.2447886
Dennis A Eichenauer, Peter Borchmann
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Abstract

Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) is a rare lymphoma entity accounting for ≈5% of all Hodgkin lymphoma (HL) cases. As some characteristics of NLPHL resemble B-cell non-Hodgkin lymphoma (B-NHL), nodular lymphocyte-predominant B-cell lymphoma has been proposed as alternative name. Unlike classical HL (cHL), NLPHL is mostly diagnosed in early stages. The clinical course is usually indolent. Overall, NLPHL patients have an excellent prognosis and the majority experiences long-term survival. Except for stage IA disease which is sufficiently treated with radiotherapy alone, treatment of newly diagnosed NLPHL is often very similar to cHL. However, activity has also been demonstrated for rituximab-containing protocols applied in B-NHL. Second-line treatment is chosen individually and mostly less intensive than in cHL. Chimeric antigen receptor T-cell therapy and bispecific antibodies may be part of future treatment strategies for NLPHL. This review aims at summarizing recent data on treatment approaches and discussing future perspectives in NLPHL.

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重新审视结节淋巴细胞为主的霍奇金淋巴瘤:当前的管理策略和未来的展望。
结节性淋巴细胞主导型霍奇金淋巴瘤(NLPHL)是一种罕见的淋巴瘤,约占所有霍奇金淋巴瘤(HL)病例的5%。由于NLPHL的某些特征类似于b细胞非霍奇金淋巴瘤(B-NHL),因此有人建议将结节性淋巴细胞为主的b细胞淋巴瘤作为替代名称。与经典HL (cHL)不同,NLPHL大多在早期诊断。临床过程通常不痛不痒。总体而言,NLPHL患者预后良好,大多数患者长期生存。除了仅用放射治疗就能充分治疗的IA期疾病外,新诊断的NLPHL的治疗通常与cHL非常相似。然而,含有利妥昔单抗的方案也被证明适用于B-NHL。二线治疗是单独选择的,其强度大多低于cHL。嵌合抗原受体t细胞疗法和双特异性抗体可能是未来NLPHL治疗策略的一部分。这篇综述旨在总结最近关于NLPHL治疗方法的数据,并讨论未来的前景。
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
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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