Endocrine · 2026
The peripheral blood lymphocyte signatures forecast therapeutic efficacy in papillary thyroid cancer patients undergoing radioactive iodine therapy.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Cao Jingjia, Sun Yaru, Xu Zihui, Lu Jia, Dong Aiqiang, Guan Xin
Аннотация
PURPOSE: This study aimed to evaluate the predictive role of peripheral blood lymphocyte subsets in therapeutic efficacy for papillary thyroid cancer (PTC) patients undergoing radioactive iodine (RAI) therapy. METHODS: A retrospective analysis was conducted on 405 PTC patients received RAI therapy. Peripheral blood lymphocyte subsets (CD3+, CD4+, CD8+ T cells, B cells, and NK cells) were measured using flow cytometry. Clinical outcomes were categorized as excellent/indeterminate response (ER/IDR) or biochemical/structural incomplete response (BIR/SIR) based on the 2015 ATA guidelines. Statistical analyses included ROC curves, Mann-Whitney U-tests, and multivariate regression. RESULTS: Lymphocyte profiles varied with clinical features: older age (≥ 55 years) correlated with reduced CD8+ T cells (P < 0.001), while BRAFV600E-positive patients showed lower CD4+ and CD3+ T cells (P = 0.02). Lymph node metastasis (N1a/b) was associated with suppressed NK cell activity (P = 0.02) but elevated T-cell percentages (P = 0.01). B-cell counts and CD4/CD8 ratios were significant predictors of RAI response. Patients with BIR/SIR exhibited higher B-cell counts (250.0 vs. 219.0 cells/µL, P = 0.001) and CD4/CD8 ratios (1.6 vs.1.4, P = 0.02) compared to patients with ER/IDR. ROC analysis demonstrated moderate predictive accuracy for B cells (AUC = 0.601, P = 0.001) and CD4/CD8 ratios (AUC = 0.567, P = 0.027). CONCLUSION: Peripheral blood lymphocyte subsets, particularly B-cell levels and CD4/CD8 ratios, may serve as biomarkers for predicting therapeutic efficacy in PTC. These findings highlight the clinical relevance of integrating immune status assessment into therapeutic decision-making, offering potential for personalized treatment strategies.