Development and validation of MRI-derived deep learning score for non-invasive prediction of PD-L1 expression and prognostic stratification in head and neck squamous cell carcinoma.

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Tác giả: Fan Bai, Genji Bai, Cong Ding, Yue Kang, Junfang Xian

Ngôn ngữ: eng

Ký hiệu phân loại: 338.9 Economic development and growth

Thông tin xuất bản: England : Cancer imaging : the official publication of the International Cancer Imaging Society , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 170257

 BACKGROUND: Immunotherapy has revolutionized the treatment landscape for head and neck squamous cell carcinoma (HNSCC) and PD-L1 combined positivity score (CPS) scoring is recommended as a biomarker for immunotherapy. Therefore, this study aimed to develop an MRI-based deep learning score (DLS) to non-invasively assess PD-L1 expression status in HNSCC patients and evaluate its potential effeciency in predicting prognostic stratification following treatment with immune checkpoint inhibitors (ICI). METHODS: In this study, we collected data from four patient cohorts comprising a total of 610 HNSCC patients from two separate institutions. We developed deep learning models based on the ResNet-101 convolutional neural network to analyze three MRI sequences (T1WI, T2WI, and contrast-enhanced T1WI). Tumor regions were manually segmented, and features extracted from different MRI sequences were fused using a transformer-based model incorporating attention mechanisms. The model's performance in predicting PD-L1 expression was evaluated using the area under the curve (AUC), sensitivity, specificity, and calibration metrics. Survival analyses were conducted using Kaplan-Meier survival curves and log-rank tests to evaluate the prognostic significance of the DLS. RESULTS: The DLS demonstrated high predictive accuracy for PD-L1 expression, achieving an AUC of 0.981, 0.860 and 0.803 in the training, internal and external validation cohort. Patients with higher DLS scores demonstrated significantly improved progression-free survival (PFS) in both the internal validation cohort (hazard ratio: 0.491
  95% CI, 0.270-0.892
  P = 0.005) and the external validation cohort (hazard ratio: 0.617
  95% CI, 0.391-0.973
  P = 0.040). In the ICI-treated cohort, the DLS achieved an AUC of 0.739 for predicting durable clinical benefit (DCB). CONCLUSIONS: The proposed DLS offered a non-invasive and accurate approach for assessing PD-L1 expression in patients with HNSCC and effectively stratified HNSCC patients to benefit from immunotherapy based on PFS.
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