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Towards a survival risk prediction model for metastatic NSCLC patients on durvalumab using whole-lung CT radiomics.
Patwardhan, Kedar A; RaviPrakash, Harish; Nikolaou, Nikolaos; Gonzalez-García, Ignacio; Salazar, José Domingo; Metcalfe, Paul; Reischl, Joachim.
Afiliação
  • Patwardhan KA; Oncology Data Science, AstraZeneca, Waltham, MA, United States.
  • RaviPrakash H; Oncology Data Science, AstraZeneca, Waltham, MA, United States.
  • Nikolaou N; Oncology Data Science, AstraZeneca, Cambridge, United Kingdom.
  • Gonzalez-García I; Clinical Pharmacology and Quantitative Pharmacology, Clinical Pharmacology and Safety Sciences, AstraZeneca, Cambridge, United Kingdom.
  • Salazar JD; Oncology Data Science, AstraZeneca, Cambridge, United Kingdom.
  • Metcalfe P; Oncology Data Science, AstraZeneca, Cambridge, United Kingdom.
  • Reischl J; Diagnostic Science, Precision Medicine, AstraZeneca, Gothenburg, Sweden.
Front Immunol ; 15: 1383644, 2024.
Article em En | MEDLINE | ID: mdl-38915397
ABSTRACT

Background:

Existing criteria for predicting patient survival from immunotherapy are primarily centered on the PD-L1 status of patients. We tested the hypothesis that noninvasively captured baseline whole-lung radiomics features from CT images, baseline clinical parameters, combined with advanced machine learning approaches, can help to build models of patient survival that compare favorably with PD-L1 status for predicting 'less-than-median-survival risk' in the metastatic NSCLC setting for patients on durvalumab. With a total of 1062 patients, inclusive of model training and validation, this is the largest such study yet.

Methods:

To ensure a sufficient sample size, we combined data from treatment arms of three metastatic NSCLC studies. About 80% of this data was used for model training, and the remainder was held-out for validation. We first trained two independent models; Model-C trained to predict survival using clinical data; and Model-R trained to predict survival using whole-lung radiomics features. Finally, we created Model-C+R which leveraged both clinical and radiomics features.

Results:

The classification accuracy (for median survival) of Model-C, Model-R, and Model-C+R was 63%, 55%, and 68% respectively. Sensitivity analysis of survival prediction across different training and validation cohorts showed concordance indices ([95 percentile]) of 0.64 ([0.63, 0.65]), 0.60 ([0.59, 0.60]), and 0.66 ([0.65,0.67]), respectively. We additionally evaluated generalization of these models on a comparable cohort of 144 patients from an independent study, demonstrating classification accuracies of 65%, 62%, and 72% respectively.

Conclusion:

Machine Learning models combining baseline whole-lung CT radiomic and clinical features may be a useful tool for patient selection in immunotherapy. Further validation through prospective studies is needed.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tomografia Computadorizada por Raios X / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Anticorpos Monoclonais Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tomografia Computadorizada por Raios X / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Anticorpos Monoclonais Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article