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Lesion-Based Radiomics Signature in Pretherapy 18F-FDG PET Predicts Treatment Response to Ibrutinib in Lymphoma.
Jimenez, Jorge E; Dai, Dong; Xu, Guofan; Zhao, Ruiyang; Li, Tengfei; Pan, Tinsu; Wang, Linghua; Lin, Yingyan; Wang, Zhangyang; Jaffray, David; Hazle, John D; Macapinlac, Homer A; Wu, Jia; Lu, Yang.
Afiliación
  • Jimenez JE; From the Departments of Imaging Physics.
  • Dai D; Nuclear Medicine, The University of Texas MD Anderson Cancer Center.
  • Xu G; Nuclear Medicine, The University of Texas MD Anderson Cancer Center.
  • Zhao R; Department of Electrical and Computer Engineering, Rice University.
  • Li T; Departments of Biostatistics.
  • Pan T; From the Departments of Imaging Physics.
  • Wang L; Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston.
  • Lin Y; Department of Electrical and Computer Engineering, Rice University.
  • Wang Z; Department of Electrical and Computer Engineering, The University of Texas at Austin, Austin, TX.
  • Jaffray D; From the Departments of Imaging Physics.
  • Hazle JD; From the Departments of Imaging Physics.
  • Macapinlac HA; Nuclear Medicine, The University of Texas MD Anderson Cancer Center.
  • Wu J; From the Departments of Imaging Physics.
  • Lu Y; Nuclear Medicine, The University of Texas MD Anderson Cancer Center.
Clin Nucl Med ; 47(3): 209-218, 2022 Mar 01.
Article en En | MEDLINE | ID: mdl-35020640
ABSTRACT

PURPOSE:

The aim of this study was to develop a pretherapy PET/CT-based prediction model for treatment response to ibrutinib in lymphoma patients. PATIENTS AND

METHODS:

One hundred sixty-nine lymphoma patients with 2441 lesions were studied retrospectively. All eligible lymphomas on pretherapy 18F-FDG PET images were contoured and segmented for radiomic analysis. Lesion- and patient-based responsiveness to ibrutinib was determined retrospectively using the Lugano classification. PET radiomic features were extracted. A radiomic model was built to predict ibrutinib response. The prognostic significance of the radiomic model was evaluated independently in a test cohort and compared with conventional PET metrics SUVmax, metabolic tumor volume, and total lesion glycolysis.

RESULTS:

The radiomic model had an area under the receiver operating characteristic curve (ROC AUC) of 0.860 (sensitivity, 92.9%, specificity, 81.4%; P < 0.001) for predicting response to ibrutinib, outperforming the SUVmax (ROC AUC, 0.519; P = 0.823), metabolic tumor volume (ROC AUC, 0.579; P = 0.412), total lesion glycolysis (ROC AUC, 0.576; P = 0.199), and a composite model built using all 3 (ROC AUC, 0.562; P = 0.046). The radiomic model increased the probability of accurately predicting ibrutinib-responsive lesions from 84.8% (pretest) to 96.5% (posttest). At the patient level, the model's performance (ROC AUC = 0.811; P = 0.007) was superior to that of conventional PET metrics. Furthermore, the radiomic model showed robustness when validated in treatment subgroups first (ROC AUC, 0.916; P < 0.001) versus second or greater (ROC AUC, 0.842; P < 0.001) line of defense and single treatment (ROC AUC, 0.931; P < 0.001) versus multiple treatments (ROC AUC, 0.824; P < 0.001).

CONCLUSIONS:

We developed and validated a pretherapy PET-based radiomic model to predict response to treatment with ibrutinib in a diverse cohort of lymphoma patients.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fluorodesoxiglucosa F18 / Linfoma Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Clin Nucl Med Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fluorodesoxiglucosa F18 / Linfoma Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Clin Nucl Med Año: 2022 Tipo del documento: Article