Evidence map›Paper›PMID 42351247›Full record

ArticleCancer imaging : the official publication of the International Cancer Imaging Society2026

A clinical-radiomic model based on best subset regression for prognostic prediction in natural killer/T-cell lymphoma.

Fangfang Tian, Longlan Chen, Xiaoliang Chen, Hua Pang

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Article in Cancer imaging : the official publication of the International Cancer Imaging Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Fangfang Tian *Department of Nuclear Medicine, The First Affiliated Hospital of Chongqing Medical University, No.1 Youyi Road, Yuzhong District, Chongqing, 400016, China.
Longlan Chen *Department of Nuclear Medicine, Chongqing University Cancer Hospital, Chongqing, 400030, China.
Xiaoliang Chen *Department of Nuclear Medicine, Chongqing University Cancer Hospital, Chongqing, 400030, China. chengxiaoliang26@163.com.
Hua Pang *Department of Nuclear Medicine, The First Affiliated Hospital of Chongqing Medical University, No.1 Youyi Road, Yuzhong District, Chongqing, 400016, China. phua1973@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe outcomes of patients with natural killer/T-cell lymphoma (NKTCL) are heterogeneous, thus, this study aimed to develop and validate prognostic models for overall survival (OS) and progression-free survival (PFS) in NKTCL by integrating clinicopathological and pre-treatment [18F]-fluorodeoxyglucose positron emission tomography/computed tomography ([18F]-FDG PET/CT)-derived variables, comparing the performance of univariate COX, least absolute shrinkage and selection operator (LASSO), and best subset regression (BSR) methods.

methodsThis retrospective study analyzed a cohort of 114 pre-treatment patients with NKTCL who have performed [18F]-FDG PET/CT scan. Predictors included clinical parameters (e.g., age, albumin (Alb)), pathological indices (e.g., Ki67), Epstein-Barr virus (EBV), and imaging metrics (e.g., radiomics score (Radscore), maximum standardized uptake value (SUV

resultsThe BSR-derived model demonstrated superior performance for predicting OS (3-year AUC: 0.883; C-index: 0.807). For OS, the optimal multivariate model identified Alb (hazard ratios (HR): 0.226, 95% confidence interval (CI): 0.073-0.697, P = 0.00961), EBV (HR: 3.826, 95% CI: 1.259-11.630, P = 0.017986), SUV

conclusionComparative analysis revealed that BSR outperformed both univariate COX regression and LASSO in selecting variables for NKTCL prognosis modeling. Using BSR, we developed a robust model integrating essential clinical factors and PET/CT-derived radiomic features (e.g., Alb, EBV, SUVmax, LLR and Radscore for OS and age, EBV and Ki67 for PFS), offering a valuable tool for risk stratification and guiding individualized treatment strategies.

Indexed as

Lymphoma, Extranodal NK-T-CellPositron Emission Tomography Computed TomographyRadiomicsAdultAgedFemaleFluorodeoxyglucose F18HumansMaleMiddle AgedPrognosisRadiopharmaceuticalsRetrospective StudiesFluorodeoxyglucose F18RadiopharmaceuticalsModel predictionNatural killer/T-cell lymphomaOverall survivalProgression-free survival

Identifiers

PMID42351247
PMCPMC13560112

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.