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B 细胞淋巴瘤中的循环肿瘤 DNA

英文原题:Circulating tumor DNA in B cell lymphomas.

查看英文原题

Circulating tumor DNA in B cell lymphomas.

PubMed 2025/07/02(内容时间) Curr Opin Oncol Q3 · IF 2.4(JCR 2025)

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研究思路按摘要原文分段

本综述评估了循环肿瘤 DNA (ctDNA) 作为淋巴瘤治疗中微创工具的重要性。

目前的文献证明 ctDNA 能够缓解标准活检和成像的缺点,提供对肿瘤负荷、克隆进化和治疗耐药性的实时洞察。在霍奇金淋巴瘤中,ctDNA 可以进行全面的基因组分析和治疗监测。在弥漫性大 B 细胞淋巴瘤 (DLBCL) 中,ctDNA 与疾病负担相关,对于追踪耐药性非常有价值,尤其是在 CAR-T 细胞治疗中。在原发性中枢神经系统淋巴瘤 (PCNSL) 和血管内大 B 细胞淋巴瘤 (IVLBCL) 等罕见亚型中,ctDNA 可以提高诊断精度并实现早期复发检测。即使在惰性淋巴瘤中,ctDNA 也可用于复发监测和风险评估。摘要:CtDNA 分析可能成为个性化淋巴瘤管理的关键要素,从而实现早期干预和量身定制的治疗策略。然而,未来的努力应集中于协调方法和验证大规模试验的结果,以使这些技术能够在常规实践中采用。

展开英文摘要原文

PURPOSE OF REVIEW: This review evaluates the importance of circulating tumor DNA (ctDNA) as a minimally invasive tool in lymphoma management. RECENT FINDINGS: Current literature demonstrates ctDNA's ability to alleviate the shortcomings of standard biopsy and imaging, providing real-time insights into tumor burden, clonal evolution, and treatment resistance. In Hodgkin lymphoma, ctDNA allows for comprehensive genomic profiling and treatment monitoring.

In diffuse large B-cell lymphoma (DLBCL), ctDNA correlates with disease burden and is valuable for tracking resistance, especially in CAR T-cell therapy. In rare subtypes like primary central nervous system lymphoma (PCNSL) and intravascular large B-cell lymphoma (IVLBCL), ctDNA enhances diagnostic precision and enables early relapse detection.

Even in indolent lymphomas, ctDNA could prove useful in relapse monitoring and risk assessment. SUMMARY: CtDNA analysis could become a key element in personalized lymphoma management, enabling earlier interventions and tailored treatment strategies.

However, future efforts should focus on harmonizing methodologies and validating findings in large-scale trials to allow these techniques to be adopted in routine practice.

论文信息

作者
Fangazio M、Dewispelaere L
第一作者单位
Haematology Department, Laboratoire Hospitalier Universitaire de Bruxelles (LHUB-ULB), Université Libre de Bruxelles, Brussels, Belgium.Belgium
文献类型
综述
期刊
Current opinion in oncology2025 Sep 1
原文标识
PubMed 40658005 · DOI 10.1097/CCO.0000000000001178