SynthesisEuropean journal of nuclear medicine and molecular imaging2026
Diagnostic performance of 18F-FDG PET/CT metabolic parameters for early prediction of pathological response in NSCLC treated with neoadjuvant immuno(chemo)therapy: A systematic review and meta-analysis.
Synthesis 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 4 papers, 2 of them syntheses that pooled it.
What it found
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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.
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Who cites it
4 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- 18F-FDG PET/CT for predicting major pathological response to neoadjuvant therapy in non-small cell lung cancer: a meta-analysis.Frontiers in oncology · 2026Pooled it
- CT-based radiomics in predicting the efficacy of preoperative neoadjuvant chemoimmunotherapy for non-small cell lung cancer: a systematic review and meta-analysis.Frontiers in immunology · 2026Pooled it
- PET/CT predict pathological response to neoadjuvant nivolumab in resectable non-small cell lung cancer.European journal of nuclear medicine and molecular imaging · 2026Article
- From imaging heterogeneity to clinical decision: a novel imaging biomarker based on bone marrow kinetics for advanced NSCLC patients in partial response.EJNMMI research · 2026Article
Corrections and comments
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Authors and funding
15 authors.
Funding
Abstract
purposeEarly and accurate prediction of pathological response in non-small cell lung cancer (NSCLC) receiving neoadjuvant immune(chemo)immunotherapy is essential for guiding treatment strategies. This meta-analysis aims to assess the predictive performance of PET/CT-derived metabolic parameters for identifying major pathological response (MPR) and pathological complete response (pCR).
methodsThe PubMed, Web of Science, Embase, and Cochrane Library were searched for related studies from inception to January 2025. Studies assessed evaluated predefined 18F-FDG PET/CT parameter (PERCIST, PERCIST-max, ΔSUVmax, ΔSULpeak, ΔSULmax, ΔMTV, ΔTLG, pre/post-treatment SUVmax, post-treatment SULmax/SULpeak) and reported pathological outcomes were included. Methodological quality was evaluated using QUADAS-2. Sensitivity, specificity and heterogeneity were analyzed via HSROC models. Publication bias was assessed via Deeks' test.
resultsSixteen studies met inclusion criteria. For MPR, PERCIST showed excellent sensitivity (1.00) but limited specificity (0.67), while PERCIST-max achieved both high sensitivity (0.92) and superior specificity (0.94). ΔSUVmax demonstrated balanced accuracy (sensitivity: 0.92; specificity: 0.77; AUC: 0.94), and ΔSULpeak also yielded high diagnostic performance (sensitivity: 0.94; specificity: 0.91). Volumetric metrics such as ΔMTV and ΔTLG showed variable results, with ΔMTV performing moderately (sensitivity: 0.77; specificity: 0.83), and ΔTLG exhibiting lower sensitivity (0.63) despite good specificity (0.81). For pCR, ΔSUVmax retained high sensitivity (0.94) but showed reduced specificity (0.57; AUC: 0.86). SUVmax-Pre showed moderate accuracy (sensitivity: 0.78; specificity: 0.81). Subgroup analyses indicated that the diagnostic performance of ΔSUVmax varied depending on treatment regimen.
conclusionsThe study support ΔSUVmax as a reliable indicator of MPR, although its specificity for pCR remains limited. PERCIST's high sensitivity aids in excluding non-responders. However, limited study numbers for parameters like ΔSULpeak, SULpeak-Post, and ΔSULmax reduce generalizability, necessitating larger validation studies to confirm their diagnostic utility.
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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.