Evidence map›Paper›PMID 41400856›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2026

Jiaona Dai, Yuheng Zou, Hui Wang, Hexiao Huang, Lixiang Yang, Bingwen Zou, Rong Tian

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In one paragraph

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. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. AlEuropean journal of nuclear medicine and molecular imaging · 2026
    Article
  2. Spatiotemporal voxel-wise concordance betweenEuropean journal of nuclear medicine and molecular imaging · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Jiaona Dai *Department of Nuclear Medicine, West China Hospital, Sichuan University, No. 37 Guoxue Alley, Chengdu, 610041, Sichuan, China.
Yuheng Zou *Department of Nuclear Medicine, West China Hospital, Sichuan University, No. 37 Guoxue Alley, Chengdu, 610041, Sichuan, China.
Hui WangDepartment of Nuclear Medicine, West China Hospital, Sichuan University, No. 37 Guoxue Alley, Chengdu, 610041, Sichuan, China.
Hexiao HuangDepartment of Nuclear Medicine, West China Hospital, Sichuan University, No. 37 Guoxue Alley, Chengdu, 610041, Sichuan, China.
Lixiang YangDepartment of Nuclear Medicine, West China Hospital, Sichuan University, No. 37 Guoxue Alley, Chengdu, 610041, Sichuan, China.
Bingwen ZouDivision of Thoracic Tumor Multimodality Treatment, Department of Radiation Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China. zoubingwen81@163.com.
Rong TianDepartment of Nuclear Medicine, West China Hospital, Sichuan University, No. 37 Guoxue Alley, Chengdu, 610041, Sichuan, China. rongtiannuclear@126.com.ORCID 0000-0002-5191-9004

Funding

the Chinese Academy of Medical Sciences Clinical and Translation Medical Program 2022-I2M-CT-B-106the Young Scientists Fund of the National Natural Science Foundation of China 82502505
6 · The paper itself

Abstract

purposeTo evaluate the predictive value of dual-tracer

methodsThis retrospective analysis of a prospective trial (ChiCTR2100051599) included patients with LA-ESCC enrolled from February 2022 to August 2024. Patients received nCRT and underwent dual-tracer PET/CT at baseline (S1) and post-treatment (before esophagectomy, S2). Intensity-, volume-, and distribution-based PET features, including total lesion glycolysis, were extracted. LASSO regression was employed for feature selection. Eight models with different variable combinations were established by logistic regression and cox regression. Associations with TRG and PFS were evaluated using receiver operating characteristic (ROC) curves, Harrell's C-index and Kaplan-Meier estimates. The models were compared pair-to-pair to identify the added value of imaging parameters.

resultsForty-nine patients (mean age 65.8 ± 5.7 years) were included. TRG 0 was achieved in 29/49 (59.2%) patients. Eleven patients (11/48, 22.9%) experienced a PFS event within the cohort. The combined model incorporating Clinical features with (S1 + S2) FAPI parameters achieved the highest AUC of 0.95 (95% confidence interval (CI): 0.84-1.00) for TRG prediction, while the Clinical + S2 FDG model demonstrated the best PFS prediction with C-index of 0.93 (95% CI: 0.82-0.97). Pairwise comparisons revealed that FAPI-based models significantly outperformed clinical-only models for TRG prediction (p = 0.003). BMI and FAPI heterogeneity parameters were independent predictors of TRG, while clinical staging and FDG distribution features predicted PFS.

conclusionBaseline FAPI PET provides superior value for predicting pathological response, while post-treatment FDG PET offers better prognostic stratification. The combination of imaging biomarkers with clinical factors might enable robust prediction of treatment outcomes in LA-ESCC.

Indexed as

ChemoradiotherapyEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaFluorodeoxyglucose F18Neoadjuvant TherapyPositron Emission Tomography Computed TomographyAgedFemaleGallium RadioisotopesHumansMaleMiddle AgedProgression-Free SurvivalRetrospective StudiesTreatment OutcomeFluorodeoxyglucose F18Gallium Radioisotopes68Ga-FAPI PET/CTEsophageal squamous cell carcinomaNeoadjuvant treatmentPathological responseProgrammed cell death protein-1 blockadeProgression-Free survival

Identifiers

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Registered trials

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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.