Fully automated volumetric assessment of tumor burden using artificial intelligence on Ga-PSMA-11 PET predicts survival after Lu-PSMA therapy in metastatic Castration-resistant prostate cancer.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
환자: mCRPC treated with ¹⁷⁷Lu-PSMA therapy were analyzed
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSION] AI-based volumetric analysis of tumor burden on PSMA PET has prognostic significance for survival in ¹⁷⁷Lu-PSMA-treated mCRPC patients. The nomogram integrating PSMA with clinical factors might help in personalized risk stratification, facilitating AI-aided therapeutic decision-making.
[PURPOSE] Despite the rapid development of artificial intelligence (AI)-powered automated segmentation tools for PET/CT imaging, their prognostic value in predicting survival outcomes remains inadequa
- p-value P < 0.001
- 95% CI 0.64-0.78
APA
Zang S, Meng Q, et al. (2026). Fully automated volumetric assessment of tumor burden using artificial intelligence on Ga-PSMA-11 PET predicts survival after Lu-PSMA therapy in metastatic Castration-resistant prostate cancer.. European journal of nuclear medicine and molecular imaging, 53(3), 1913-1926. https://doi.org/10.1007/s00259-025-07628-x
MLA
Zang S, et al.. "Fully automated volumetric assessment of tumor burden using artificial intelligence on Ga-PSMA-11 PET predicts survival after Lu-PSMA therapy in metastatic Castration-resistant prostate cancer.." European journal of nuclear medicine and molecular imaging, vol. 53, no. 3, 2026, pp. 1913-1926.
PMID
41111086 ↗
Abstract 한글 요약
[PURPOSE] Despite the rapid development of artificial intelligence (AI)-powered automated segmentation tools for PET/CT imaging, their prognostic value in predicting survival outcomes remains inadequately assessed. Our objective was to explore the prognostic significance of tumor burden quantification derived from PSMA PET/CT using AI for metastatic castration-resistant prostate cancer (mCRPC) patients receiving Lutetium-177 (¹⁷⁷Lu) PSMA therapy.
[METHODS] A retrospective cohort of 107 consecutive patients with mCRPC treated with ¹⁷⁷Lu-PSMA therapy were analyzed. Utilizing a deep learning algorithm, PSMA-positive lesions were automatically delineated on baseline 68Ga-PSMA-11 PET/CT scans. Key metrics were derived from the segmented lesions: total tumor volume (PSMA), total tumor load (PSMA = PSMA × SUV), and total tumor quotient (PSMA = PSMA / SUV). A prognostic nomogram was developed through Cox regression analysis, incorporating LASSO regularization for variable selection.
[RESULTS] Univariate analysis revealed that higher PSMA (HR 1.26), PSMA (HR 1.18), and PSMA (HR 1.29) were significantly associated with shorter overall survival (OS). A prognostic nomogram that integrated PSMA alongside chemotherapy history, hemoglobin levels, alkaline phosphatase, and prostate-specific antigen demonstrated a bootstrap-corrected C-index of 0.71 (95% CI 0.64-0.78). Risk stratification using the nomogram showed significantly prolonged OS in low-risk vs. high-risk groups (median OS 30.9 vs. 7.9 months; HR 0.25, 95% CI 0.13-0.45, P < 0.001). The retrospective design is a study limitation.
[CONCLUSION] AI-based volumetric analysis of tumor burden on PSMA PET has prognostic significance for survival in ¹⁷⁷Lu-PSMA-treated mCRPC patients. The nomogram integrating PSMA with clinical factors might help in personalized risk stratification, facilitating AI-aided therapeutic decision-making.
[METHODS] A retrospective cohort of 107 consecutive patients with mCRPC treated with ¹⁷⁷Lu-PSMA therapy were analyzed. Utilizing a deep learning algorithm, PSMA-positive lesions were automatically delineated on baseline 68Ga-PSMA-11 PET/CT scans. Key metrics were derived from the segmented lesions: total tumor volume (PSMA), total tumor load (PSMA = PSMA × SUV), and total tumor quotient (PSMA = PSMA / SUV). A prognostic nomogram was developed through Cox regression analysis, incorporating LASSO regularization for variable selection.
[RESULTS] Univariate analysis revealed that higher PSMA (HR 1.26), PSMA (HR 1.18), and PSMA (HR 1.29) were significantly associated with shorter overall survival (OS). A prognostic nomogram that integrated PSMA alongside chemotherapy history, hemoglobin levels, alkaline phosphatase, and prostate-specific antigen demonstrated a bootstrap-corrected C-index of 0.71 (95% CI 0.64-0.78). Risk stratification using the nomogram showed significantly prolonged OS in low-risk vs. high-risk groups (median OS 30.9 vs. 7.9 months; HR 0.25, 95% CI 0.13-0.45, P < 0.001). The retrospective design is a study limitation.
[CONCLUSION] AI-based volumetric analysis of tumor burden on PSMA PET has prognostic significance for survival in ¹⁷⁷Lu-PSMA-treated mCRPC patients. The nomogram integrating PSMA with clinical factors might help in personalized risk stratification, facilitating AI-aided therapeutic decision-making.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
- Humans
- Male
- Prostatic Neoplasms
- Castration-Resistant
- Gallium Isotopes
- Aged
- Retrospective Studies
- Lutetium
- Tumor Burden
- Gallium Radioisotopes
- Positron Emission Tomography Computed Tomography
- Middle Aged
- Oligopeptides
- Artificial Intelligence
- Automation
- Neoplasm Metastasis
- Radioisotopes
- 80 and over
- Edetic Acid
- Prognosis
- Dipeptides
- Prostate-Specific Antigen
- 177Lu-PSMA therapy
- Artificial intelligence
… 외 3개
같은 제1저자의 인용 많은 논문 (3)
- Correction: RARS1 inhibits ENO1 ubiquitination and degradation to protect against ferroptosis in hepatocellular carcinoma.
- Construction of a macrophage-related prognostic signature and assessment of immune checkpoint inhibitor efficacy of HCC.
- RARS1 inhibits ENO1 ubiquitination and degradation to protect against ferroptosis in hepatocellular carcinoma.
🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반
- A Phase I Study of Hydroxychloroquine and Suba-Itraconazole in Men with Biochemical Relapse of Prostate Cancer (HITMAN-PC): Dose Escalation Results.
- Self-management of male urinary symptoms: qualitative findings from a primary care trial.
- Clinical and Liquid Biomarkers of 20-Year Prostate Cancer Risk in Men Aged 45 to 70 Years.
- Diagnostic accuracy of Ga-PSMA PET/CT versus multiparametric MRI for preoperative pelvic invasion in the patients with prostate cancer.
- Comprehensive analysis of androgen receptor splice variant target gene expression in prostate cancer.
- Clinical Presentation and Outcomes of Patients Undergoing Surgery for Thyroid Cancer.