4.6 Article

Detection of ovarian cancer via the spectral fingerprinting of quantum-defect-modified carbon nanotubes in serum by machine learning

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NATURE BIOMEDICAL ENGINEERING
卷 6, 期 3, 页码 267-+

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NATURE PORTFOLIO
DOI: 10.1038/s41551-022-00860-y

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资金

  1. NIH [R01-CA215719, U54-CA137788, U54-CA132378, P30-CA008748, R01-GM114167, 201708320366]
  2. National Science Foundation CAREER Award [1752506]
  3. Honorable Tina Brozman Foundation for Ovarian Cancer Research
  4. Tina Brozman Ovarian Cancer Research Consortium 2.0
  5. Kelly Auletta Fund for Ovarian Cancer Research
  6. American Cancer Society Research Scholar Grant [GC230452]
  7. Pershing Square Sohn Cancer Research Alliance
  8. Expect Miracles Foundation - Financial Services Against Cancer
  9. Experimental Therapeutics Center
  10. Commonwealth Foundation for Cancer Research
  11. China Scholarships Council (CSC) [201708320366]
  12. University of Maryland
  13. NIST
  14. Dean's Fellowship at Lehigh University
  15. Directorate For Engineering
  16. Div Of Chem, Bioeng, Env, & Transp Sys [1752506] Funding Source: National Science Foundation

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Ovarian cancer can be accurately predicted using a disease fingerprint obtained through machine learning from the spectra of near-infrared fluorescence emissions of a carbon nanotube sensor array.
Ovarian cancer can be predicted with high sensitivity and specificity via a fingerprint obtained, via machine learning, from near-infrared fluorescence emissions of an array of carbon nanotube sensors in serum samples. Serum biomarkers are often insufficiently sensitive or specific to facilitate cancer screening or diagnostic testing. In ovarian cancer, the few established serum biomarkers are highly specific, yet insufficiently sensitive to detect early-stage disease and to impact the mortality rates of patients with this cancer. Here we show that a 'disease fingerprint' acquired via machine learning from the spectra of near-infrared fluorescence emissions of an array of carbon nanotubes functionalized with quantum defects detects high-grade serous ovarian carcinoma in serum samples from symptomatic individuals with 87% sensitivity at 98% specificity (compared with 84% sensitivity at 98% specificity for the current best clinical screening test, which uses measurements of cancer antigen 125 and transvaginal ultrasonography). We used 269 serum samples to train and validate several machine-learning classifiers for the discrimination of patients with ovarian cancer from those with other diseases and from healthy individuals. The predictive values of the best classifier could not be attained via known protein biomarkers, suggesting that the array of nanotube sensors responds to unidentified serum biomarkers.

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