ArticleEuropean journal of nuclear medicine and molecular imaging2026
Integrated [
Article in European journal of nuclear medicine and molecular imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Radionuclide-based pharmaceuticals for breast cancer imaging: state of the art.EJNMMI radiopharmacy and chemistry · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
14 authors.
Funding
Abstract
purposeThis study assessed the diagnostic efficacy of fluorine-18-labeled fibroblast activation protein inhibitor 42 ([
methodsA prospective study enrolled 64 women with BI-RADS 4 or 5 lesions identified through mammography or ultrasound. All participants underwent contrast-enhanced [
resultsThe study included 114 breast lesions (89 malignant, 25 benign) and 114 lymph node groups (82 malignant, 32 benign). In detecting primary breast lesions, the quantitative PET/MR based on TBR (PET/MR-TBR) demonstrated superior specificity over breast MRI (96% vs. 68%, P = 0.016), corresponding to a marked reduction in false positive rate from 32% (8/25) to 4.0% (1/25; P = 0.027), while maintaining comparable sensitivity (94% vs. 97%, P = 1.00). For BI-RADS 3/4 lesions on breast MRI, PET/MR-TBR achieved an AUC of 0.90, with a significant NRI of 90.5% (P = 0.018) for BI-RADS 4 lesions. For breast lesions smaller than 10 mm, PET/MR-TBR increased specificity to 94% versus 75% for breast MRI (P > 0.05). For axillary lymph node evaluation, the quantitative PET/MR based on SUV
conclusion[
Indexed as
Identifiers
40802091What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.