分析细胞游离 DNA 预测结直肠癌患者贝伐珠单抗治疗效果

IF 4.7 2区 医学 Q1 GENETICS & HEREDITY NPJ Genomic Medicine Pub Date : 2024-05-29 DOI:10.1038/s41525-024-00415-x
Tom Venken, Ian S Miller, Ingrid Arijs, Valentina Thomas, Ana Barat, Johannes Betge, Tianzuo Zhan, Timo Gaiser, Matthias P Ebert, Alice C O'Farrell, Jochen Prehn, Rut Klinger, Darran P O'Connor, Brian Moulton, Verena Murphy, Garazi Serna, Paolo G Nuciforo, Ray McDermott, Brian Bird, Gregory Leonard, Liam Grogan, Anne Horgan, Nadine Schulte, Markus Moehler, Diether Lambrechts, Annette T Byrne
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引用次数: 0

摘要

为了预测贝伐单抗(BVZ)联合疗法的疗效,我们采用了无细胞DNA(cfDNA)来测定转移性结直肠癌(mCRC)患者的染色体不稳定性(CIN)、核糖体足迹(NF)和甲基化图谱。低覆盖率全基因组测序(LC-WGS)是从 AC-ANGIOPREDICT II 期试验(NCT01822444)中收集的 74 例 mCRC 患者的匹配肿瘤和血浆样本中进行的,并对 CIN 和 NF 进行了分析。曼海姆大学医学中心(UMM)的验证队列血浆样本也进行了类似分析。在 BVZ 治疗前和治疗后收集的 61 份 AC-ANGIOPREDICT 血浆样本被选中进行靶向甲基化测序。利用 cfDNA CIN 图谱,AC-ANGIOPREDICT 样本以 92.3% 的准确率被亚型为低 CIN 和高 CIN 群组,并观察到匹配血浆和肿瘤之间具有良好的一致性。据观察,CIN 高的患者生存率有所提高。基于血浆的CIN分类在UMM队列中得到了验证。甲基化分析确定了低CIN与高CIN的差异(AUC = 0.87)。此外,BVZ 后甲基化评分的明显降低与预后的改善有关(p = 0.013)。分析血浆样本中 cfDNA 的 CIN、NFs 和甲基化图谱有助于对 CIN 群组进行分层,从而为患者的治疗反应提供依据。
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Analysis of cell free DNA to predict outcome to bevacizumab therapy in colorectal cancer patients.

To predict outcome to combination bevacizumab (BVZ) therapy, we employed cell-free DNA (cfDNA) to determine chromosomal instability (CIN), nucleosome footprints (NF) and methylation profiles in metastatic colorectal cancer (mCRC) patients. Low-coverage whole-genome sequencing (LC-WGS) was performed on matched tumor and plasma samples, collected from 74 mCRC patients from the AC-ANGIOPREDICT Phase II trial (NCT01822444), and analysed for CIN and NFs. A validation cohort of plasma samples from the University Medical Center Mannheim (UMM) was similarly profiled. 61 AC-ANGIOPREDICT plasma samples collected before and following BVZ treatment were selected for targeted methylation sequencing. Using cfDNA CIN profiles, AC-ANGIOPREDICT samples were subtyped with 92.3% accuracy into low and high CIN clusters, with good concordance observed between matched plasma and tumor. Improved survival was observed in CIN-high patients. Plasma-based CIN clustering was validated in the UMM cohort. Methylation profiling identified differences in CIN-low vs. CIN high (AUC = 0.87). Moreover, significant methylation score decreases following BVZ was associated with improved outcome (p = 0.013). Analysis of CIN, NFs and methylation profiles from cfDNA in plasma samples facilitates stratification into CIN clusters which inform patient response to treatment.

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来源期刊
NPJ Genomic Medicine
NPJ Genomic Medicine Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.40
自引率
1.90%
发文量
67
审稿时长
17 weeks
期刊介绍: npj Genomic Medicine is an international, peer-reviewed journal dedicated to publishing the most important scientific advances in all aspects of genomics and its application in the practice of medicine. The journal defines genomic medicine as "diagnosis, prognosis, prevention and/or treatment of disease and disorders of the mind and body, using approaches informed or enabled by knowledge of the genome and the molecules it encodes." Relevant and high-impact papers that encompass studies of individuals, families, or populations are considered for publication. An emphasis will include coupling detailed phenotype and genome sequencing information, both enabled by new technologies and informatics, to delineate the underlying aetiology of disease. Clinical recommendations and/or guidelines of how that data should be used in the clinical management of those patients in the study, and others, are also encouraged.
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