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Letter to the Editor: An ultra-sensitive assay using cell-free DNA fragmentomics for multi-cancer early detection.
Bao, Hua; Wang, Zheng; Ma, Xiaoji; Guo, Wei; Zhang, Xiangyu; Tang, Wanxiangfu; Chen, Xin; Wang, Xinyu; Chen, Yikuan; Mo, Shaobo; Liang, Naixin; Ma, Qianli; Wu, Shuyu; Xu, Xiuxiu; Chang, Shuang; Wei, Yulin; Zhang, Xian; Bao, Hairong; Liu, Rui; Yang, Shanshan; Jiang, Ya; Wu, Xue; Li, Yaqi; Zhang, Long; Tan, Fengwei; Xue, Qi; Liu, Fangqi; Cai, Sanjun; Gao, Shugeng; Peng, Junjie; Zhou, Jian; Shao, Yang.
Affiliation
  • Bao H; Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, 210000, Jiangsu, China.
  • Wang Z; Department of Liver Surgery and Transplantation, Liver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
  • Ma X; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, Shanghai, 200032, China.
  • Guo W; Shanghai Key Laboratory of Organ Transplantation, Zhongshan Hospital, Fudan University, Fudan University, 130 Fenglin Road, Shanghai, 200032, China.
  • Zhang X; Department of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
  • Tang W; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
  • Chen X; Department of Thoracic Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
  • Wang X; Key Laboratory of Minimally Invasive Therapy Research for Lung Cancer, Chinese Academy of Medical Sciences, Beijing, 100730, China.
  • Chen Y; Department of Liver Surgery and Transplantation, Liver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
  • Mo S; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, Shanghai, 200032, China.
  • Liang N; Shanghai Key Laboratory of Organ Transplantation, Zhongshan Hospital, Fudan University, Fudan University, 130 Fenglin Road, Shanghai, 200032, China.
  • Ma Q; Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, 210000, Jiangsu, China.
  • Wu S; Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, 210000, Jiangsu, China.
  • Xu X; Department of Liver Surgery and Transplantation, Liver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
  • Chang S; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, Shanghai, 200032, China.
  • Wei Y; Shanghai Key Laboratory of Organ Transplantation, Zhongshan Hospital, Fudan University, Fudan University, 130 Fenglin Road, Shanghai, 200032, China.
  • Zhang X; Department of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
  • Bao H; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
  • Liu R; Department of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
  • Yang S; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
  • Jiang Y; Department of Thoracic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, 100730, China.
  • Wu X; Department of Thoracic Surgery, China-Japan Friendship Hospital, Beijing, 100029, China.
  • Li Y; Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, 210000, Jiangsu, China.
  • Zhang L; Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, 210000, Jiangsu, China.
  • Tan F; Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, 210000, Jiangsu, China.
  • Xue Q; Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, 210000, Jiangsu, China.
  • Liu F; Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, 210000, Jiangsu, China.
  • Cai S; Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, 210000, Jiangsu, China.
  • Gao S; Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, 210000, Jiangsu, China.
  • Peng J; Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, 210000, Jiangsu, China.
  • Zhou J; Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, 210000, Jiangsu, China.
  • Shao Y; Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, 210000, Jiangsu, China.
Mol Cancer ; 21(1): 129, 2022 06 11.
Article in En | MEDLINE | ID: mdl-35690859
ABSTRACT
Early detection can benefit cancer patients with more effective treatments and better prognosis, but existing early screening tests are limited, especially for multi-cancer detection. This study investigated the most prevalent and lethal cancer types, including primary liver cancer (PLC), colorectal adenocarcinoma (CRC), and lung adenocarcinoma (LUAD). Leveraging the emerging cell-free DNA (cfDNA) fragmentomics, we developed a robust machine learning model for multi-cancer early detection. 1,214 participants, including 381 PLC, 298 CRC, 292 LUAD patients, and 243 healthy volunteers, were enrolled. The majority of patients (N = 971) were at early stages (stage 0, N = 34; stage I, N = 799). The participants were randomly divided into a training cohort and a test cohort in a 11 ratio while maintaining the ratio for the major histology subtypes. An ensemble stacked machine learning approach was developed using multiple plasma cfDNA fragmentomic features. The model was trained solely in the training cohort and then evaluated in the test cohort. Our model showed an Area Under the Curve (AUC) of 0.983 for differentiating cancer patients from healthy individuals. At 95.0% specificity, the sensitivity of detecting all cancer reached 95.5%, while 100%, 94.6%, and 90.4% for PLC, CRC, and LUAD, individually. The cancer origin model demonstrated an overall 93.1% accuracy for predicting cancer origin in the test cohort (97.4%, 94.3%, and 85.6% for PLC, CRC, and LUAD, respectively). Our model sensitivity is consistently high for early-stage and small-size tumors. Furthermore, its detection and origin classification power remained superior when reducing sequencing depth to 1× (cancer detection ≥ 91.5% sensitivity at 95.0% specificity; cancer origin ≥ 91.6% accuracy). In conclusion, we have incorporated plasma cfDNA fragmentomics into the ensemble stacked model and established an ultrasensitive assay for multi-cancer early detection, shedding light on developing cancer early screening in clinical practice.
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Full text: 1 Database: MEDLINE Main subject: Colorectal Neoplasms / Cell-Free Nucleic Acids Type of study: Clinical_trials / Diagnostic_studies / Prognostic_studies / Screening_studies Limits: Humans Language: En Year: 2022 Type: Article

Full text: 1 Database: MEDLINE Main subject: Colorectal Neoplasms / Cell-Free Nucleic Acids Type of study: Clinical_trials / Diagnostic_studies / Prognostic_studies / Screening_studies Limits: Humans Language: En Year: 2022 Type: Article