靶向治疗慢性淋巴细胞白血病击中治疗靶心

IF 21 1区 医学 Q1 HEMATOLOGY
Blood Pub Date : 2025-06-02 DOI:10.1182/blood.2025028570
William G Wierda, Barbara F Eichhorst, Michael J Hallek
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引用次数: 0

摘要

慢性淋巴细胞白血病(CLL)是一种具有临床和生物学异质性的疾病;一些患者观察多年无症状,而另一些患者则迅速发展为需要治疗的进行性疾病。通过治疗,一些患者最终发展为耐药CLL或转化为侵袭性CLL。在整个谱系中,患者经历与感染和二次癌症风险增加相关的免疫功能障碍,从而导致疾病的发病率和死亡率。CLL的最终治疗目标是消除疾病并实现免疫恢复。部分接受一线化疗免疫治疗(FCR)的患者,部分接受限时联合靶向治疗的患者,以及部分接受同种异体干细胞移植的复发/难治性CLL患者,有可能实现疾病消除。这些患者的长期免疫恢复是难以捉摸的。目前的靶向治疗,包括联合使用BTK-和bcl2 -抑制剂以及CD20单克隆抗体,可以产生特殊的治疗效果,从而提高需要治疗的患者的生存率。虽然在高效CLL管理方面取得了明显进展,但由于该疾病的慢性性质,对这些进展的全面影响的评估需要时间。此外,必须确保全球获得靶向治疗,强调需要在全球范围内协调监管和负担得起的治疗方案。在这里,我们讨论了研究和合作策略,以改进靶向药物的使用,以消除CLL并恢复所有受影响个体的免疫功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hitting the Therapeutic Bullseye with Targeted Therapy for Patients with Chronic Lymphocytic Leukemia.

Chronic lymphocytic leukemia (CLL) is a disease of great clinical and biologic heterogeneity; some patients are observed for years without symptoms, while others rapidly develop progressive disease requiring treatment. With therapy, some patients eventually develop resistant CLL or transformation to an aggressive form. Across this spectrum, patients experience immune dysfunction associated with increased risk for infection and second cancers, contributing to morbidity and mortality of the disease. The ultimate therapeutic bullseye for CLL is to eliminate the disease and achieve immune restoration. Disease elimination can potentially be achieved for a fraction of patients treated first-line with chemoimmunotherapy (FCR), for some patients who receive time-limited combined targeted therapy, and for some patients with relapsed/refractory CLL who undergo allogeneic stem cell transplant. Long-term immune restoration for these patients is elusive. Current targeted therapies, including BTK- and BCL2-inhibitors and CD20 monoclonal antibodies used in combinations, can produce exceptional therapeutic outcomes, which are improving survival for patients who need treatment. While clear progress has been made toward highly effective CLL management, appreciation of the full impact of these advances will require time due to the chronic nature of the disease. Additionally, it is imperative to ensure global access to the targeted therapies, emphasizing the need for harmonized regulatory oversight and affordable treatment options worldwide. Here, we discuss research and collaborative strategies to refine the use of targeted agents to eliminate CLL and restore immune function for all affected individuals.

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来源期刊
Blood
Blood 医学-血液学
CiteScore
23.60
自引率
3.90%
发文量
955
审稿时长
1 months
期刊介绍: Blood, the official journal of the American Society of Hematology, published online and in print, provides an international forum for the publication of original articles describing basic laboratory, translational, and clinical investigations in hematology. Primary research articles will be published under the following scientific categories: Clinical Trials and Observations; Gene Therapy; Hematopoiesis and Stem Cells; Immunobiology and Immunotherapy scope; Myeloid Neoplasia; Lymphoid Neoplasia; Phagocytes, Granulocytes and Myelopoiesis; Platelets and Thrombopoiesis; Red Cells, Iron and Erythropoiesis; Thrombosis and Hemostasis; Transfusion Medicine; Transplantation; and Vascular Biology. Papers can be listed under more than one category as appropriate.
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