MZL的药物开发:照顾被遗忘的孩子。

IF 23.1 1区 医学 Q1 HEMATOLOGY
Blood Pub Date : 2025-09-17 DOI:10.1182/blood.2024028270
Catherine Thieblemont,Sylvain Carras,Côme Bommier
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引用次数: 0

摘要

边缘带淋巴瘤(MZL)包括生物异质性的惰性b细胞淋巴瘤,在临床研究中仍未得到充分代表。尽管最近b细胞恶性肿瘤的治疗取得了重大进展,但MZL的试验设计仍然面临着持续的挑战,包括诊断异质性、不一致的对照组、次优终点和经济障碍。在本文中,我们研究了这些关键障碍,并讨论了克服这些障碍的新策略,如诊断标准的标准化,亚型特异性治疗方法的实施,替代终点的验证,以及新的反应评估模式的整合,如代谢成像(正电子发射断层扫描),流式细胞术或单细胞分子评估中的最小残留疾病评估,以及循环肿瘤DNA测量。我们认为MZL应该被理解为一种方法论范例,而不是临床的例外。这可能有助于改进试验设计,并最终加速治疗创新,跨越广泛的惰性淋巴瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug development in MZL: caring for the forgotten child.
Marginal zone lymphoma (MZL) encompasses biologically heterogenous group of indolent B-cell lymphomas that remains substantially underrepresented in clinical research. Despite recent and significant therapeutic advancess in B-cell malignancies, trial design in MZL continues to face persistent challenges including diagnostic heterogeneity, inconsistent control arms, suboptimal endpoints, and economic barriers. In this narrative review, we examine these key obstacles and discuss emerging strategies to overcome them, such as the standardization of diagnostic criteria, implementation of subtype-specific treatment approaches, validation of surrogate endpoints, and integration of novel response assessment modalities such as metabolic imaging (positron emission tomography), minimal residual disease assessment in flow cytometry or single cell molecular evaluation, and circulating tumor DNA measurement, but need to be evaluated and harmonized for full appreciation We contend that MZL should be understood as a methodological paradigm, rather than as a clinical exception. This may facilitate the refinement of trial design and ultimately accelerate therapeutic innovation across the broad spectrum of indolent lymphomas.
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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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