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Improving Prediction of Survival and Progression in Metastatic Non-Small Cell Lung Cancer After Immunotherapy Through Machine Learning of Circulating Tumor DNA.
Ding, Haolun; Xu, Xu Steven; Yang, Yaning; Yuan, Min.
Afiliación
  • Ding H; Department of Statistics and Finance, School of Management, University of Science and Technology of China, Hefei, Anhui, China.
  • Xu XS; Clinical Pharmacology and Quantitative Science, Genmab Inc, Princeton, NJ.
  • Yang Y; Department of Statistics and Finance, School of Management, University of Science and Technology of China, Hefei, Anhui, China.
  • Yuan M; Department of Health Data Science, Anhui Medical University, Hefei, Anhui, China.
JCO Precis Oncol ; 8: e2300718, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38976829
ABSTRACT

PURPOSE:

To use modern machine learning approaches to enhance and automate the feature extraction from the longitudinal circulating tumor DNA (ctDNA) data and to improve the prediction of survival and disease progression, risk stratification, and treatment strategies for patients with 1L non-small cell lung cancer (NSCLC). MATERIALS AND

METHODS:

Using IMpower150 trial data on patients with untreated metastatic NSCLC treated with atezolizumab and chemotherapies, we developed a machine learning algorithm to extract predictive features from ctDNA kinetics, improving survival and progression prediction. We analyzed kinetic data from 17 ctDNA summary markers, including cell-free DNA concentration, allele frequency, tumor molecules in plasma, and mutation counts.

RESULTS:

Three hundred and ninety-eight patients with ctDNA data (206 in training and 192 in validation) were analyzed. Our models outperformed existing workflow using conventional temporal ctDNA features, raising overall survival (OS) concordance index to 0.72 and 0.71 from 0.67 and 0.63 for C3D1 and C4D1, respectively, and substantially improving progression-free survival (PFS) to approximately 0.65 from the previous 0.54-0.58, a 12%-20% increase. Additionally, they enhanced risk stratification for patients with NSCLC, achieving clear OS and PFS separation. Distinct patterns of ctDNA kinetic characteristics (eg, baseline ctDNA markers, depth of ctDNA responses, and timing of ctDNA clearance, etc) were revealed across the risk groups. Rapid and complete ctDNA clearance appears essential for long-term clinical benefit.

CONCLUSION:

Our machine learning approach offers a novel tool for analyzing ctDNA kinetics, extracting critical features from longitudinal data, improving our understanding of the link between ctDNA kinetics and progression/mortality risks, and optimizing personalized immunotherapies for 1L NSCLC.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Progresión de la Enfermedad / Aprendizaje Automático / ADN Tumoral Circulante / Inmunoterapia / Neoplasias Pulmonares Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JCO Precis Oncol Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Progresión de la Enfermedad / Aprendizaje Automático / ADN Tumoral Circulante / Inmunoterapia / Neoplasias Pulmonares Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JCO Precis Oncol Año: 2024 Tipo del documento: Article País de afiliación: China