Non-invasive minimal residual disease detection of liver cancer using circulating tumor DNA features and α-fetoprotein: A prospective study.

229 Background: Liver cancer hasahigh recurrence rate of 50%-70% for early-stage patients. Minimal residual disease (MRD) is closely correlated with cancer early recurrence. Here, we developed SeekInCure, a non-invasive assay to detect MRD and predict the prognosis of liver cancer patients after radical surgery. Methods: 32 liver cancer patients undergoing radical surgery were prospectively enrolled. 8 mL peripheral blood was collected from each patient before and after surgery, respectively. SeekInCure assay, which integrated the protein tumor marker (AFP) and cancer genomic hallmarks: copy number aberration, and fragment size from ctDNA to calculate a score (P HCC ), was utilized to detect the cancer signal in each blood sample. MRD status determined by P HCC value was correlated with the clinical outcome (OS) and the benefit of treatment after radical surgery. Results: Out of the 32 liver cancer patients, 78.1% (25/32) were at early stages (Stages I/II: 65.6%/12.5%), and 59.4% (19/32) received systemic treatment after surgery. MTB- patients (12.5%, 4/32) showed better overall survival (OS) than MTB+ patients (87.4%, 28/32) with a high hazard ratio (HR) value of 1.19. After radical surgery, 23 HCC patients were MRD-, including 4 MTB- patients remaining negative; meanwhile, 9 out of 28 MTB+ patients remained MRD+. The OS of MRD- patients was significantly better than that of MRD+ patients (HR 5.67; 95% confidence interval (CI), 1.33 ~ 24.20; P = 0.008). Moreover, the OS of MRD- patients with and without systemic treatment showed no significant difference (P = 0.930). Conclusions: This prospective study demonstrated the potential clinical value of ctDNA in detecting MRD status to predict the prognosis in early-stage liver cancer patients and to identify patients who may benefit from avoiding overtreatment. This strategy requires validation in independent prospective studies.

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Journal
Journal of Clinical Oncology
Published
2024-08-10
DOI
https://doi.org/10.1200/jco.2024.42.23_suppl.229
Primary Topic
Cancer Genomics and Diagnostics
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article
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article

Non-invasive minimal residual disease detection of liver cancer using circulating tumor DNA features and α-fetoprotein: A prospective study.

Guanghui Long, Yinyin Chang, Qingqi Ren, Liangliang Zhang et al.
Journal of Clinical Oncology
Cancer Genomics and Diagnostics
article

Non-invasive minimal residual disease detection of liver cancer using circulating tumor DNA features and α-fetoprotein: A prospective study.

Guanghui Long, Yinyin Chang, Qingqi Ren, Liangliang Zhang, Shiyong Li, Yumin Feng, Mao Mao
article en

Abstract

229 Background: Liver cancer hasahigh recurrence rate of 50%-70% for early-stage patients. Minimal residual disease (MRD) is closely correlated with cancer early recurrence. Here, we developed SeekInCure, a non-invasive assay to detect MRD and predict the prognosis of liver cancer patients after radical surgery. Methods: 32 liver cancer patients undergoing radical surgery were prospectively enrolled. 8 mL peripheral blood was collected from each patient before and after surgery, respectively. SeekInCure assay, which integrated the protein tumor marker (AFP) and cancer genomic hallmarks: copy number aberration, and fragment size from ctDNA to calculate a score (P HCC ), was utilized to detect the cancer signal in each blood sample. MRD status determined by P HCC value was correlated with the clinical outcome (OS) and the benefit of treatment after radical surgery. Results: Out of the 32 liver cancer patients, 78.1% (25/32) were at early stages (Stages I/II: 65.6%/12.5%), and 59.4% (19/32) received systemic treatment after surgery. MTB- patients (12.5%, 4/32) showed better overall survival (OS) than MTB+ patients (87.4%, 28/32) with a high hazard ratio (HR) value of 1.19. After radical surgery, 23 HCC patients were MRD-, including 4 MTB- patients remaining negative; meanwhile, 9 out of 28 MTB+ patients remained MRD+. The OS of MRD- patients was significantly better than that of MRD+ patients (HR 5.67; 95% confidence interval (CI), 1.33 ~ 24.20; P = 0.008). Moreover, the OS of MRD- patients with and without systemic treatment showed no significant difference (P = 0.930). Conclusions: This prospective study demonstrated the potential clinical value of ctDNA in detecting MRD status to predict the prognosis in early-stage liver cancer patients and to identify patients who may benefit from avoiding overtreatment. This strategy requires validation in independent prospective studies.

Journal of Clinical OncologyVol. 42(23_suppl)
Peking University Shenzhen Hospital (CN)
Good health and well-being
Openalex Percentile: Top 80%
Cancer Genomics and Diagnostics
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