Next-Generation Sequencing–Based Testing Among Patients With Advanced or Metastatic Nonsquamous Non–Small Cell Lung Cancer in the United States: Predictive Modeling Using Machine Learning Methods
Notice bibliographique
Résumé
BACKGROUND: Next-generation sequencing (NGS) has become a cornerstone of treatment for lung cancer and is recommended in current treatment guidelines for patients with advanced or metastatic disease. OBJECTIVE: This study was designed to use machine learning methods to determine demographic and clinical characteristics of patients with advanced or metastatic non-small cell lung cancer (NSCLC) that may predict likelihood of receiving NGS-based testing (ever vs never NGS-tested) as well as likelihood of timing of testing (early vs late NGS-tested). METHODS: Deidentified patient-level data were analyzed in this study from a real-world cohort of patients with advanced or metastatic NSCLC in the United States. Patients with nonsquamous disease, who received systemic therapy for NSCLC, and had at least 3 months of follow-up data for analysis were included in this study. Three strategies, logistic regression models, penalized logistic regression using least absolute shrinkage and selection operator penalty, and extreme gradient boosting with classification trees as base learners, were used to identify predictors of ever versus never and early versus late NGS testing. Data were split into D1 (training+validation; 80%) and D2 (testing; 20%) sets; the 3 strategies were evaluated by comparing their performance on multiple m=1000 splits in the training (70%) and validation data (30%) within the D1 set. The final model was selected by evaluating performance using the area under the receiver operating curve while taking into account considerations of simplicity and clinical interpretability. Performance was re-estimated using the test data D2. RESULTS: A total of 13,425 met the criteria for the ever NGS-tested, and 17,982 were included in the never NGS-tested group. Performance metrics showed the area under the receiver operating curve evaluated from validation data was similar across all models (77%-84%). Among those in the ever NGS-tested group, 84.08% (n=11,289) were early NGS-tested, and 15.91% (n=2136) late NGS-tested. Factors associated with both ever having NGS testing as well as early NGS testing included later year of NSCLC diagnosis, no smoking history, and evidence of programmed death ligand 1 testing (all P<.05). Factors associated with a greater chance of never receiving NGS testing included older age, lower performance status, Black race, higher number of single-gene tests, public insurance, and treatment in a geography with Molecular Diagnostics Services Program adoption (all P<.05). CONCLUSIONS: Predictors of ever versus never as well as early versus late NGS testing in the setting of advanced or metastatic NSCLC were consistent across machine learning methods in this study, demonstrating the ability of these models to identify factors that may predict NGS-based testing. There is a need to ensure that patients regardless of age, race, insurance status, and geography (factors associated with lower odds of receiving NGS testing in this study) are provided with equitable access to NGS-based testing.
Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.
Comment cette classification a été obtenuedéplier
Prédiction distillée sur la base complète
Imitation des enseignantsNi prévalence calibrée, ni vérité terrain. Validation humaine à venir. Apprise à partir de 10 348 étiquettes directes de Codex et de 10 348 étiquettes directes de Gemma. Le mode candidate est l'union des têtes enseignantes seuillées; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont ni des étiquettes humaines ni des étiquettes directes de modèles de pointe.
Scores Codex et Gemma par catégorie
| Catégorie | Codex | Gemma |
|---|---|---|
| Métarecherche | 0,000 | 0,000 |
| Méta-épidémiologie (sens strict) | 0,000 | 0,000 |
| Méta-épidémiologie (sens large) | 0,000 | 0,000 |
| Bibliométrie | 0,000 | 0,002 |
| Études des sciences et des technologies | 0,000 | 0,000 |
| Communication savante | 0,000 | 0,000 |
| Science ouverte | 0,000 | 0,000 |
| Intégrité de la recherche | 0,000 | 0,000 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,000 | 0,000 |
Scores machine (provisoires)
Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.
Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.
score_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découleClassification
machine, non validéePrédiction automatique; un appel candidat d’une seule tête enseignante, pas un consensus.
Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».