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局部晚期食管癌新辅助放化疗后循环肿瘤 DNA 的检测。

Detection of circulating tumour DNA after neoadjuvant chemoradiotherapy in patients with locally advanced oesophageal cancer.

机构信息

Department of Surgery, Erasmus MC Cancer Institute, University Medical Centre Rotterdam, Rotterdam, The Netherlands.

Department of Medical Oncology, Erasmus MC Cancer Institute, University Medical Centre Rotterdam, Rotterdam, The Netherlands.

出版信息

J Pathol. 2023 Jan;259(1):35-45. doi: 10.1002/path.6016. Epub 2022 Oct 31.

Abstract

Active surveillance instead of standard surgery after neoadjuvant chemoradiotherapy (nCRT) has been proposed for patients with oesophageal cancer. Circulating tumour DNA (ctDNA) may be used to facilitate selection of patients for surgery. We show that detection of ctDNA after nCRT seems highly suggestive of major residual disease. Tumour biopsies and blood samples were taken before, and 6 and 12 weeks after, nCRT. Biopsies were analysed with regular targeted next-generation sequencing (NGS). Circulating cell-free DNA (cfDNA) was analysed using targeted NGS with unique molecular identifiers and digital polymerase chain reaction. cfDNA mutations matching pre-treatment biopsy mutations confirmed the presence of ctDNA. In total, 31 patients were included, of whom 24 had a biopsy mutation that was potentially detectable in cfDNA (77%). Pre-treatment ctDNA was detected in nine of 24 patients (38%), four of whom had incurable disease progression before surgery. Pre-treatment ctDNA detection had a sensitivity of 47% (95% CI 24-71) (8/17), specificity of 85% (95% CI 42-99) (6/7), positive predictive value (PPV) of 89% (95% CI 51-99) (8/9), and negative predictive value (NPV) of 40% (95% CI 17-67) (6/15) for detecting major residual disease (>10% residue in the resection specimen or progression before surgery). After nCRT, ctDNA was detected in three patients, two of whom had disease progression. Post-nCRT ctDNA detection had a sensitivity of 21% (95% CI 6-51) (3/14), specificity of 100% (95% CI 56-100) (7/7), PPV of 100% (95% CI 31-100) (3/3), and NPV of 39% (95% CI 18-64) (7/18) for detecting major residual disease. The addition of ctDNA to the current set of diagnostics did not lead to more patients being clinically identified with residual disease. These results indicate that pre-treatment and post-nCRT ctDNA detection may be useful in identifying patients at high risk of disease progression. The addition of ctDNA analysis to the current set of diagnostic modalities may not improve detection of residual disease after nCRT. © 2022 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

摘要

新辅助放化疗(nCRT)后采用主动监测而非标准手术已被提议用于食管癌患者。循环肿瘤 DNA(ctDNA)可用于帮助选择手术患者。我们表明,nCRT 后 ctDNA 的检测似乎高度提示存在主要残留疾病。在 nCRT 之前、之后 6 周和 12 周采集肿瘤活检和血样。活检采用常规靶向下一代测序(NGS)进行分析。使用带有独特分子标识符和数字聚合酶链反应的靶向 NGS 分析循环无细胞 DNA(cfDNA)。与预处理活检突变匹配的 cfDNA 突变证实了 ctDNA 的存在。总共纳入 31 名患者,其中 24 名患者的活检突变可在 cfDNA 中检测到(77%)。24 名患者中有 9 名(38%)在术前检测到术前 ctDNA,其中 4 名在术前发生无法治愈的疾病进展。术前 ctDNA 检测的敏感性为 47%(95%CI24-71)(8/17),特异性为 85%(95%CI42-99)(6/7),阳性预测值(PPV)为 89%(95%CI51-99)(8/9),阴性预测值(NPV)为 40%(95%CI17-67)(6/15),用于检测主要残留疾病(切除标本中>10%残留或术前进展)。nCRT 后,3 名患者检测到 ctDNA,其中 2 名患者疾病进展。nCRT 后 ctDNA 检测的敏感性为 21%(95%CI6-51)(3/14),特异性为 100%(95%CI56-100)(7/7),阳性预测值为 100%(95%CI31-100)(3/3),阴性预测值为 39%(95%CI18-64)(7/18),用于检测主要残留疾病。ctDNA 的加入并没有导致更多的患者被临床诊断为残留疾病。这些结果表明,术前和 nCRT 后 ctDNA 检测可用于识别疾病进展风险较高的患者。ctDNA 分析的加入可能不会提高 nCRT 后残留疾病的检出率。©2022 作者。《病理学杂志》由 John Wiley & Sons Ltd 代表英国和爱尔兰的病理学学会出版。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1c0/10092085/5b2a372be45c/PATH-259-35-g002.jpg

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