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Improving the predictive value of end-of-treatment PET/CT in diffuse large B-cell lymphoma.

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Haematologica 📖 저널 OA 66.9% 2021: 1/1 OA 2024: 1/1 OA 2025: 24/56 OA 2026: 143/196 OA 2021~2026 2026 OA
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PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
5 patients were analyzed.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Adding baseline features did not notably impact the models' performance. Our models could support more accurate response-adapted treatment decisions, reducing unnecessary subsequent false positive-directed treatments to just 7%.

Bes AL, Zwezerijnen GJC, Heymans MW, Dührsen U, Eertink JJ, Wiegers SE, Lugtenburg PJ, Hüttmann A, Kurch L, Hanoun C, Mikhaeel GN, Ceriani L, Zucca E, Czibor S, Györke T, Chamuleau MED, Fanti S, Lee ST, Hoekstra OS, Zijlstra JM, Barrington SF, Boellaard R

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The 5-point Deauville score (DS) assesses end-of-treatment (EOT) response on PET/CT in diffuse large B-cell lymphoma patients, categorizing scans as 'positive' or 'negative' for complete metabolic res

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↓ .bib ↓ .ris
APA Bes AL, Zwezerijnen GJC, et al. (2026). Improving the predictive value of end-of-treatment PET/CT in diffuse large B-cell lymphoma.. Haematologica. https://doi.org/10.3324/haematol.2025.288821
MLA Bes AL, et al.. "Improving the predictive value of end-of-treatment PET/CT in diffuse large B-cell lymphoma.." Haematologica, 2026.
PMID 41504226 ↗

Abstract

The 5-point Deauville score (DS) assesses end-of-treatment (EOT) response on PET/CT in diffuse large B-cell lymphoma patients, categorizing scans as 'positive' or 'negative' for complete metabolic response. However, the positive predictive value (PPV) is suboptimal at 60%. We evaluated whether quantitative PET parameters combined with clinical data could improve prediction of treatment failure in EOT PET-positive patients. Baseline and EOT PET/CT scans of 138 DS4-5 patients were analyzed. Lesions were segmented using a semi-automated adaptive method (SUV4.0 or MV3). PET parameters, including total metabolic tumor volume (TMTV), number of lesions (NOL), tumorSUV/liverSUV-ratio (TLR), the maximum distance between the largest and any other lesion (DmaxBulk), and changes over time, were obtained. Two Cox regression models predicted 2-year progression-free survival. Clinical data were combined with EOT PET in model 1, and baseline, EOT and delta values in model 2. After internal bootstrapping, models were evaluated for classification using different risk-of-progression cutoffs. Sensitivity, specificity, PPV and negative predictive values (NPV) were determined. Using forward selection, model 1 comprised two variables: the NOL and the tumorSUVpeak/liverSUVmean (TLRpeakmean) at EOT (AIC=690.072, c-index=0.747). Model 2 incorporated NOL, TLRpeakmean (EOT) and baseline SUVmean (AIC=687.064, c-index=0.762). The PPV improved to over 85% without compromising the NPV. False positives dropped from 54 (39%, by DS) to 9 (7%) and 6 (4%) for models 1 and 2, respectively. Adding baseline features did not notably impact the models' performance. Our models could support more accurate response-adapted treatment decisions, reducing unnecessary subsequent false positive-directed treatments to just 7%.
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