Evidence map›Paper›PMID 41678503›Full record

ArticlePloS one2026

Al18F-NOTA-FAPI-04 PET/CT for diagnosis of breast cancer and its correlation with pathological features: A single-center retrospective study.

Yi Wang, Lijuan Feng, Limeng He, Nan Liu, Hao Wang

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Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Yi WangDepartment of Nuclear Medicine, Zigong Fourth People's Hospital, Zigong, Sichuan, China.
Lijuan FengDepartment of Nuclear Medicine, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
Limeng HeDepartment of Nuclear Medicine, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
Nan LiuDepartment of Nuclear Medicine, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
Hao WangDepartment of Nuclear Medicine, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.ORCID https://orcid.org/0009-0007-3487-5795

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo systematically evaluate the diagnostic efficacy of Al¹⁸F-NOTA-FAPI-04 PET/CT in breast cancer and explore the correlation between tracer uptake parameters and pathological features of breast cancer based on single-centre, retrospective data.

methodsThis single-center retrospective study enrolled 58 female patients with suspected primary breast cancer who underwent Al¹⁸F-NOTA-FAPI-04 PET/CT before surgery or core needle biopsy (February 2023-November 2025). Lesion maximum/mean standardized uptake values (SUVmax/SUVmean) were measured via region-of-interest analysis. Semi-quantitative positivity thresholds (SUVmax > 2.5 or tumor-to-background ratio ≥ 1.5) were used for lesion classification. Diagnostic efficacy (sensitivity, specificity, accuracy) was calculated with pathological results as the gold standard, and 95% confidence intervals (CIs) were determined via the Clopper-Pearson exact method. Differences in uptake parameters across pathological types, molecular subtypes, and immunohistochemical (ER/PR/HER2/Ki-67) statuses were analyzed using Mann-Whitney U or Kruskal-Wallis H tests.

resultsOf 58 patients, 49 had breast cancer and 9 had benign lesions. Al¹⁸F-NOTA-FAPI-04 PET/CT achieved a sensitivity of 95.9% (95% CI: 86.3%-99.5%), specificity of 88.9% (95% CI: 51.9%-99.7%), and accuracy of 94.8% (95% CI: 85.8%-98.9%). All 53 primary lesions were detected (detection rate: 100%), and the detection rate for 87 lymph node metastases was 96.5%. SUVmax/SUVmean of malignant lesions (median [IQR]: 13.20 [9.55-17.85]/8.15 [5.68-10.92]) were significantly higher than those of benign lesions (2.13 [1.56-2.89]/1.35 [0.98-1.86], both P < 0.001). No statistically significant differences in uptake parameters were observed across pathological types, molecular subtypes, or ER/PR/HER2/Ki-67 statuses (all P > 0.05), though numerical trends existed; this may be attributed to Type II error due to small subgroup sizes and insufficient statistical power (29.7%-62.3% for detecting medium-to-large effect sizes). No correlation was found between lesion size and uptake parameters (r = 0.186 for SUVmax, r = 0.165 for SUVmean, both P > 0.05).

conclusionAl¹⁸F-NOTA-FAPI-04 PET/CT exhibits high sensitivity and accuracy for breast cancer diagnosis and lymph node metastasis detection, with uptake independent of blood glucose levels. Its core clinical roles include complementary initial diagnosis in high-risk subgroups (dense breasts, diabetes), primary nodal staging, and problem-solving in equivocal cases. However, the lack of significant correlation between uptake parameters and pathological features should be interpreted cautiously due to potential Type II error. These characteristics make it a versatile imaging tool for breast cancer diagnosis and staging in regional tertiary care settings, with further validation needed in larger, balanced cohorts.

Indexed as

Breast NeoplasmsPositron Emission Tomography Computed TomographyRadiopharmaceuticalsAdultAgedFemaleFluorine RadioisotopesHumansMiddle AgedRetrospective StudiesSensitivity and SpecificityFluorine RadioisotopesRadiopharmaceuticals

Identifiers

PMID41678503
PMCPMC12900296

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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 OpenQuestion graph.