A blood-based metabolic signature for earlier detection of lung cancer
7 affiliations
- 1Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
- 2Department of Pneumology and Thoracic Oncology, Tenon Hospital, Assistance Publique–Hôpitaux de Paris, and Paris-Est Créteil University, Inserm, IMRB, Créteil, France
- 3Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
- 4Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
- 5Department of Lymphoma-Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
- 6Biostatistics Program, Public Health Science Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA
- 7Department of General Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
Abstract
Metabolomic profiling was applied to 1,259 sera collected within five years of a lung cancer diagnosis and 8,470 non-case sera from ever-smoker participants in the Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial to identify metabolic signatures for the earlier detection of lung cancer. We develop a panel of five lung cancer-associated metabolites (L5MetP: diacetylspermine, creatine riboside, arginine, hypoxanthine, and acylcarnitine C18:1) to assess 1-year risk of lung cancer. In the testing set, the L5MetP achieves an area under the receiver operating characteristic curve (AUC) of 0.79 (95% CI: 0.76–0.82) for 1-year risk of lung cancer. The L5MetP also complements existing clinical risk models that predict risk incident lung cancer as well as those that predict death from lung cancer. The L5MetP provides a means for identifying ever-smoker individuals who are lung cancer to inform on the need for lung cancer screening.
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BibTeX
@article{irajizad2026bloodbased,
title = {{A blood-based metabolic signature for earlier detection of lung cancer}},
author = {Ehsan Irajizad and Hamid Khoshfekr Rudsari and Sebastien Gendarme and Jody Vykoukal and Ranran Wu and Jennifer B. Dennison and Nastaran Karimi and Faezeh Darbaniyan and Seyed Javad Moghaddam and Kim-Anh Do and Ziding Feng and Edwin Ostrin and Samir Hanash and Johannes F. Fahrmann},
journal = {Cell Reports Medicine},
year = {2026},
month = sep,
doi = {10.1016/j.xcrm.2026.103059},
url = {https://doi.org/10.1016/j.xcrm.2026.103059},
note = {CC BY-NC-ND 4.0},
}
RIS
TY - JOUR
TI - A blood-based metabolic signature for earlier detection of lung cancer
AU - Ehsan Irajizad
AU - Hamid Khoshfekr Rudsari
AU - Sebastien Gendarme
AU - Jody Vykoukal
AU - Ranran Wu
AU - Jennifer B. Dennison
AU - Nastaran Karimi
AU - Faezeh Darbaniyan
AU - Seyed Javad Moghaddam
AU - Kim-Anh Do
AU - Ziding Feng
AU - Edwin Ostrin
AU - Samir Hanash
AU - Johannes F. Fahrmann
PY - 2026
DA - 2026/09/23
JO - Cell Reports Medicine
DO - 10.1016/j.xcrm.2026.103059
UR - https://doi.org/10.1016/j.xcrm.2026.103059
AB - Metabolomic profiling was applied to 1,259 sera collected within five years of a lung cancer diagnosis and 8,470 non-case sera from ever-smoker participants in the Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial to identify metabolic signatures for the earlier detection of lung cancer. We develop a panel of five lung cancer-associated metabolites (L5MetP: diacetylspermine, creatine riboside, arginine, hypoxanthine, and acylcarnitine C18:1) to assess 1-year risk of lung cancer. In the testing set, the L5MetP achieves an area under the receiver operating characteristic curve (AUC) of 0.79 (95% CI: 0.76–0.82) for 1-year risk of lung cancer. The L5MetP also complements existing clinical risk models that predict risk incident lung cancer as well as those that predict death from lung cancer. The L5MetP provides a means for identifying ever-smoker individuals who are lung cancer to inform on the need for lung cancer screening.
SN - 2666-3791
ER -