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循环肿瘤DNA是血管免疫母细胞性T细胞淋巴瘤反应的生物标志物。

Circulating Tumour DNA Is a Biomarker of Response in Angioimmunoblastic T-Cell Lymphoma.

作者信息

Yannakou Costas Kleanthes, Wu Simon, Rajah Karthik, Abeyakoon Chathuri, Nguyen-Ngo Caitlyn, Yap Yan Zhuang, Sheldon James, Blombery Piers, Prince Henry Miles

机构信息

Epworth HealthCare, Melbourne 3002, Australia.

Department of Clinical Pathology, The University of Melbourne, Melbourne 3010, Australia.

出版信息

Int J Mol Sci. 2025 Jul 13;26(14):6719. doi: 10.3390/ijms26146719.

Abstract

Angioimmunoblastic T-cell lymphoma (AITL) is a rare and aggressive subtype of non-Hodgkin lymphoma, the monitoring of which is largely restricted to radiological methods. Diagnosis relies on identifying characteristic clinicopathological features, supported by the detection of recurrent somatic mutations in , , and . The characteristic molecular profile of AITL and the high levels of circulating tumour DNA (ctDNA) measurable in AITL before treatment makes this an attractive lymphoma subtype in which to further investigate the role of ctDNA monitoring. The detection of somatic mutations in pre-treatment AITL-containing tissue samples was compared to those detected in pre-treatment ctDNA samples in a cohort of 12 patients. Changes in ctDNA somatic mutation burden over time were then correlated with radiological response. All six paired pre-treatment ctDNA and tissue samples had variants in common. All (8/8) previously ctDNA-detectable and variants were undetectable in ctDNA samples at the time of end-of-treatment complete metabolic response (CMR). In comparison, the majority of both previously ctDNA-detectable variants (3/4) and variants (6/11) were detectable in ctDNA samples at the time of end-of-treatment CMR. These observations suggest that / variants may be more reliable markers of measurable residual disease in AITL than / variants.

摘要

血管免疫母细胞性T细胞淋巴瘤(AITL)是一种罕见且侵袭性的非霍奇金淋巴瘤亚型,对其监测主要局限于放射学方法。诊断依赖于识别特征性的临床病理特征,并通过检测 、 、 和 中的复发性体细胞突变来支持。AITL的特征性分子谱以及治疗前AITL中可测量的高水平循环肿瘤DNA(ctDNA),使得这成为一个有吸引力的淋巴瘤亚型,可进一步研究ctDNA监测的作用。在一组12例患者中,将含AITL的治疗前组织样本中的体细胞突变检测结果与治疗前ctDNA样本中的检测结果进行了比较。然后将ctDNA体细胞突变负担随时间的变化与放射学反应相关联。所有6对治疗前ctDNA和组织样本都有共同的变异。在治疗结束时达到完全代谢缓解(CMR)时,所有(8/8)先前在ctDNA中可检测到的 和 变异在ctDNA样本中均不可检测。相比之下,在治疗结束时达到CMR时,大多数先前在ctDNA中可检测到的 变异(3/4)和 变异(6/11)在ctDNA样本中仍可检测到。这些观察结果表明,与 / 变异相比, / 变异可能是AITL中可测量残留疾病更可靠的标志物。

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