Evidence map›Paper›PMID 41816385›Full record

ArticleJournal of thoracic disease2026

The value of positron emission tomography scan in predicting pathologic response of non-small cell lung cancer managed by neoadjuvant chemo-immunotherapy.

Louis-Emmanuel Chriqui, Maged Zaher, Etienne Abdelnour-Berchtold, Hasna Bouchaab, Nuria Mederos, Sabina Berezowska, Michel Gonzalez, Matthieu Zellweger, Solange Peters, Thorsten Krueger and 2 more

Abstract read
In one paragraph

Article in Journal of thoracic disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Louis-Emmanuel Chriqui *Division of Thoracic Surgery, Lausanne University Hospital, Lausanne, Switzerland.
Maged Zaher *Division of Nuclear Medicine and Molecular Imaging, Lausanne University Hospital, Lausanne, Switzerland.
Etienne Abdelnour-BerchtoldDivision of Thoracic Surgery, Lausanne University Hospital, Lausanne, Switzerland.
Hasna BouchaabDivision of Oncology, Lausanne University Hospital, Lausanne, Switzerland.
Nuria MederosDivision of Oncology, Lausanne University Hospital, Lausanne, Switzerland.
Sabina BerezowskaDepartment of Laboratory Medicine and Pathology, Institute of Pathology, Lausanne University Hospital, Lausanne, Switzerland.
Michel GonzalezDivision of Thoracic Surgery, Lausanne University Hospital, Lausanne, Switzerland.
Matthieu ZellwegerDivision of Thoracic Surgery, Lausanne University Hospital, Lausanne, Switzerland.
Solange PetersDivision of Oncology, Lausanne University Hospital, Lausanne, Switzerland.
Thorsten KruegerDivision of Thoracic Surgery, Lausanne University Hospital, Lausanne, Switzerland.
Niklaus SchaeferDivision of Nuclear Medicine and Molecular Imaging, Lausanne University Hospital, Lausanne, Switzerland.
Jean Yannis PerentesDivision of Thoracic Surgery, Lausanne University Hospital, Lausanne, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Neoadjuvant chemo-immunotherapy improves overall survival in resectable stage II-III non-small cell lung cancer (NSCLC). Post-induction re-staging remains challenging and typically relies on contrast-enhanced computed tomography (CT). We assessed the predictive value of Methods: We analyzed all stage II-III, node-positive NSCLC patients from a collected database [2017-2023] who received neoadjuvant chemo-immunotherapy followed by surgery, with pre- and post-induction cancer assessment by Results: Seventeen women and 20 men (mean age 64±7 years) had mostly stage III adenocarcinomas. Open lobectomies (59%) were the most common procedures. Ninety-two percent of resections were R0. Major pathologic response (MPR) and pathologic complete response (pCR) occurred in 51% and 30% of patients, respectively. Mean/max tumor ΔSUV predicted pCR [area under the curve (AUC) =0.8135, P=0.004/AUC =0.8086, P=0.005] but mean/max lymph node ΔSUV predicted pCR better (AUC =0.9044, P<0.001/AUC =0.8990, P<0.001). A 70% decrease in lymph node ΔSUVmax between pre- and post-induction PET/CT predicted pCR with a sensitivity of 88% and a specificity of 78% and correlated with patient overall survival. Conclusions: Significant decrease in lymph node ΔSUVmax on PET/CT after neoadjuvant chemo-immunotherapy strongly predict pCR and overall survival. Further prospective validation is required.

Indexed as

immunotherapyLung cancerpositron emission tomography/computed tomography scan (PET/CT scan)surgery

Identifiers

PMID41816385
PMCPMC12972787

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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.