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DOI 10.1016/j.jtcvs.2022.12.014

Медицинская библиотека · The Journal of thoracic and cardiovascular surgery · 2022

Improving lung cancer diagnosis with cancer, fungal, and imaging biomarkers.

Marmor Hannah N, Kammer Michael N, Deppen Stephen A, Shipe Maren, Welty Valerie F, Patel Khushbu, Godfrey Caroline, Billatos Ehab, Herman James G, Wilson David O, Kussrow Amanda K, Bornhop Darryl J, Maldonado Fabien, Chen Heidi, Grogan Eric L

СтатьяПоддержка NIH: внешняя программаПеревод в очереди

Аннотация

OBJECTIVE

Indeterminate pulmonary nodules (IPNs) represent a significant diagnostic burden in health care. We aimed to compare a combination clinical prediction model (Mayo Clinic model), fungal (histoplasmosis serology), imaging (computed tomography [CT] radiomics), and cancer (high-sensitivity cytokeratin fraction 21; hsCYFRA 21-1) biomarker approach to a validated prediction model in diagnosing lung cancer.

METHODS

A prospective specimen collection, retrospective blinded evaluation study was performed in 3 independent cohorts with 6- to 30-mm IPNs (n = 281). Serum histoplasmosis immunoglobulin G and immunoglobulin M antibodies and hsCYFRA 21-1 levels were measured and a validated CT radiomic score was calculated. Multivariable logistic regression models were estimated with Mayo Clinic model variables, histoplasmosis antibody levels, CT radiomic score, and hsCYFRA 21-1. Diagnostic performance of the combination model was compared with that of the Mayo Clinic model. Bias-corrected clinical net reclassification index (cNRI) was used to estimate the clinical utility of a combination biomarker approach.

RESULTS

A total of 281 patients were included (111 from a histoplasmosis-endemic region). The combination biomarker model including the Mayo Clinic model score, histoplasmosis antibody levels, radiomics, and hsCYFRA 21-1 level showed improved diagnostic accuracy for IPNs compared with the Mayo Clinic model alone with an area under the receiver operating characteristics curve of 0.80 (95% CI, 0.76-0.84) versus 0.72 (95% CI, 0.66-0.78). Use of this combination model correctly reclassified intermediate risk IPNs into low- or high-risk category (cNRI benign = 0.11 and cNRI malignant = 0.16).

CONCLUSIONS

The addition of cancer, fungal, and imaging biomarkers improves the diagnostic accuracy for IPNs. Integrating a combination biomarker approach into the diagnostic algorithm of IPNs might decrease unnecessary invasive testing of benign nodules and reduce time to diagnosis for cancer.

Для цитирования: Marmor Hannah N, Kammer Michael N, Deppen Stephen A, Shipe Maren, Welty Valerie F, Patel Khushbu, Godfrey Caroline, Billatos Ehab, Herman James G, Wilson David O, Kussrow Amanda K, Bornhop Darryl J, Maldonado Fabien, Chen Heidi, Grogan Eric L. Improving lung cancer diagnosis with cancer, fungal, and imaging biomarkers.. The Journal of thoracic and cardiovascular surgery. 2022. DOI: 10.1016/j.jtcvs.2022.12.014.

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