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J Immunother Cancer. 2021 Mar;9(3). doi: 10.1136/jitc-2020-001504.
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Correlations between baseline F-FDG PET tumour parameters and circulating DNA in diffuse large B cell lymphoma and Hodgkin lymphoma.弥漫性大B细胞淋巴瘤和霍奇金淋巴瘤中基线F-FDG PET肿瘤参数与循环DNA之间的相关性
EJNMMI Res. 2020 Oct 7;10(1):120. doi: 10.1186/s13550-020-00717-y.
3
Correlation of Iodine Quantification and FDG Uptake in Early Therapy Response Assessment of Non-small Cell Lung Cancer: Possible Benefit of Dual-energy CT Scan as an Integral Part of PET/CT Examination.碘定量与 FDG 摄取在非小细胞肺癌早期治疗反应评估中的相关性:双能 CT 扫描作为 PET/CT 检查的一个组成部分可能具有获益。
Anticancer Res. 2020 Jun;40(6):3459-3468. doi: 10.21873/anticanres.14332.
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Circulating tumor DNA clearance predicts prognosis across treatment regimen in a large real-world longitudinally monitored advanced non-small cell lung cancer cohort.在一个大型真实世界纵向监测的晚期非小细胞肺癌队列中,循环肿瘤DNA清除情况可预测不同治疗方案下的预后。
Transl Lung Cancer Res. 2020 Apr;9(2):269-279. doi: 10.21037/tlcr.2020.03.17.
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Targeted genotyping of circulating tumor DNA for classical Hodgkin lymphoma monitoring: a prospective study.用于经典型霍奇金淋巴瘤监测的循环肿瘤DNA靶向基因分型:一项前瞻性研究。
Haematologica. 2021 Jan 1;106(1):154-162. doi: 10.3324/haematol.2019.237719.
6
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Clinical implications of circulating cell-free DNA quantification and metabolic tumor burden in advanced non-small cell lung cancer.循环游离 DNA 定量和代谢肿瘤负荷在晚期非小细胞肺癌中的临床意义。
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Non-invasive monitoring of diffuse large B-cell lymphoma by cell-free DNA high-throughput targeted sequencing: analysis of a prospective cohort.采用游离 DNA 高通量靶向测序对弥漫性大 B 细胞淋巴瘤进行无创监测:前瞻性队列分析。
Blood Cancer J. 2018 Aug 1;8(8):74. doi: 10.1038/s41408-018-0111-6.
10
Correlation between circulating tumour DNA and metabolic tumour burden in metastatic melanoma patients.循环肿瘤 DNA 与转移性黑色素瘤患者代谢肿瘤负担的相关性。
BMC Cancer. 2018 Jul 9;18(1):726. doi: 10.1186/s12885-018-4637-6.

循环肿瘤 DNA 与 F-FDG PET/CT 联合用于晚期非小细胞肺癌患者治疗反应的精准监测:一项前瞻性研究。

Combination of Circulating Tumour DNA and F-FDG PET/CT for Precision Monitoring of Therapy Response in Patients With Advanced Non-small Cell Lung Cancer: A Prospective Study.

机构信息

Department of Oncology and Radiotherapeutics, Faculty of Medicine and University Hospital in Pilsen, Charles University, Pilsen, Czech Republic;

Laboratory of Cancer Treatment and Tissue Regeneration, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.

出版信息

Cancer Genomics Proteomics. 2022 Mar-Apr;19(2):270-281. doi: 10.21873/cgp.20319.

DOI:10.21873/cgp.20319
PMID:35181593
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8865037/
Abstract

BACKGROUND/AIM: Circulating tumour DNA (ctDNA) represents an emerging biomarker in non-small cell lung cancer (NSCLC). We focused on the combination of ctDNA and positron emission tomography/computed tomography (PET/CT) in the follow-up monitoring of advanced-stage NSCLC patients treated with chemotherapy.

PATIENTS AND METHODS

Eighty-four patients were enrolled in this study. F-fluorodeoxyglucose PET/CT and ctDNA assessments were performed at baseline and after two cycles of chemotherapy (follow-up).

RESULTS

There was a correlation of ctDNA with metabolic tumour volume (MTV), total lesion glycolysis (TLG), and iodine concentration (IC) at baseline (p=0.001, p=0.001, p=0.003) and at follow-up (p=0.006, p=0.002, p=0.001). The objective response was associated with follow-up ctDNA (p<0.001) and the change of all PET/CT parameters. ROC analyses showed that the combination of follow-up ctDNA with changes in SUVmax is very promising for the estimation of objective response and progression-free survival.

CONCLUSION

The combination of ctDNA assessment with PET/CT is a promising approach for the follow-up monitoring of therapy response and prognosis estimation of advanced-stage NSCLC patients.

摘要

背景/目的:循环肿瘤 DNA(ctDNA)是非小细胞肺癌(NSCLC)的一种新兴生物标志物。我们专注于 ctDNA 与正电子发射断层扫描/计算机断层扫描(PET/CT)联合应用于接受化疗的晚期 NSCLC 患者的随访监测。

患者与方法

本研究纳入了 84 例患者。在基线和化疗两个周期后(随访)进行 F-氟脱氧葡萄糖 PET/CT 和 ctDNA 评估。

结果

ctDNA 与基线时的代谢肿瘤体积(MTV)、总病灶糖酵解(TLG)和碘浓度(IC)(p=0.001、p=0.001、p=0.003)以及随访时的 MTV、TLG 和 IC 相关(p=0.006、p=0.002、p=0.001)。客观缓解与随访时的 ctDNA(p<0.001)和所有 PET/CT 参数的变化相关。ROC 分析表明,随访时 ctDNA 与 SUVmax 变化的联合对评估客观缓解和无进展生存期具有很大的潜力。

结论

ctDNA 评估与 PET/CT 的联合是一种很有前途的方法,可用于晚期 NSCLC 患者的治疗反应随访监测和预后评估。