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Multimodal Artificial Intelligence-Based Virtual Biopsy for Diagnosing Abdominal Lavage Cytology-Positive Gastric Cancer.

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Advanced science (Weinheim, Baden-Wurttemberg, Germany) 📖 저널 OA 90.1% 2023: 1/1 OA 2024: 12/12 OA 2025: 148/154 OA 2026: 265/306 OA 2023~2026 2025 Vol.12(15) p. e2411490
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유사 논문
P · Population 대상 환자/모집단
152 patients, the model maintained superior predictive performance (AUC = 0.
I · Intervention 중재 / 시술
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C · Comparison 대조 / 비교
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O · Outcome 결과 / 결론
These findings suggest that the RSA model offers a reliable, non-invasive diagnostic tool for gastric cancer, capable of improving early detection and treatment outcomes. Further prospective studies are warranted to explore its full clinical potential.

Ding P, Yang J, Guo H, Wu J, Wu H, Li T

📝 환자 설명용 한 줄

Gastric cancer with peritoneal dissemination remains a significant clinical challenge due to its poor prognosis and difficulty in early detection.

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APA Ding P, Yang J, et al. (2025). Multimodal Artificial Intelligence-Based Virtual Biopsy for Diagnosing Abdominal Lavage Cytology-Positive Gastric Cancer.. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 12(15), e2411490. https://doi.org/10.1002/advs.202411490
MLA Ding P, et al.. "Multimodal Artificial Intelligence-Based Virtual Biopsy for Diagnosing Abdominal Lavage Cytology-Positive Gastric Cancer.." Advanced science (Weinheim, Baden-Wurttemberg, Germany), vol. 12, no. 15, 2025, pp. e2411490.
PMID 39985379 ↗

Abstract

Gastric cancer with peritoneal dissemination remains a significant clinical challenge due to its poor prognosis and difficulty in early detection. This study introduces a multimodal artificial intelligence-based risk stratification assessment (RSA) model, integrating radiomic and clinical data to predict peritoneal lavage cytology-positive (GC-CY1) in gastric cancer patients. The RSA model is trained and validated across retrospective, external, and prospective cohorts. In the training cohort, the RSA model achieved an area under the curve (AUC) of 0.866, outperforming traditional clinical and radiomic feature models. External validation cohorts confirmed its robustness, with AUC values of 0.883 and 0.823 for predicting peritoneal metastasis and recurrence, respectively. In a prospective validation involving 152 patients, the model maintained superior predictive performance (AUC = 0.835). The RSA model also demonstrated significant clinical benefits by effectively identifying high-risk patients likely to benefit from specific treatments, such as paclitaxel-based conversion therapy. These findings suggest that the RSA model offers a reliable, non-invasive diagnostic tool for gastric cancer, capable of improving early detection and treatment outcomes. Further prospective studies are warranted to explore its full clinical potential.

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