Evidence map›Paper›PMID 37441877›Full record

ArticleESMO open2023

Neoadjuvant treatment does not influence PD-L1 expression in stage III non-small-cell lung cancer: a retrospective analysis of tumor samples from the trials SAKK 16/96, 16/00, 16/01, and 16/14.

D König, S Savic Prince, S Hayoz, P Zens, S Berezowska, W Jochum, E Stauffer, V Braunersreuther, B Trachsel, S Thierstein and 13 more

Open access · goldAbstract read
In one paragraph

Article in ESMO open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 18% of its field
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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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

23 authors at 13 institutions in 2 countries.

D KönigDepartment of Medical Oncology, University Hospital Basel, Basel. Electronic address: david.koenig@usb.ch.
S Savic PrinceInstitute of Pathology and Medical Genetics, University Hospital Basel, Basel.
S HayozSwiss Group for Clinical Cancer Research, Bern.
P ZensInstitute of Pathology, University of Bern, Bern; Graduate School for Health Science, University of Bern, Bern.
S BerezowskaInstitute of Pathology, Centre Hospitalier Universitaire Vaudois (CHUV) and University of Lausanne, Lausanne.
W JochumInstitute of Pathology, Cantonal Hospital of St. Gallen, St. Gallen.
E StaufferInstitute of Pathology, Promed, Marly.
V BraunersreutherInstitute of Pathology, University Hospital Geneva (HUG), Geneva.
B TrachselSwiss Group for Clinical Cancer Research, Bern.
S ThiersteinSwiss Group for Clinical Cancer Research, Bern.
M MarkDepartment of Oncology, Cantonal Hospital of Graubünden, Chur.
S SchmidDepartment of Medical Oncology, University Hospital of Bern (Inselspital), Bern.
A Curioni-FontecedroClinics of Medical Oncology, Cantonal Hospital of Fribourg (HFR), Fribourg.
A AddeoDepartment of Oncology/Hematology, University Hospital Geneva (HUG), Geneva.
I OpitzDepartment of Thoracic Surgery, University Hospital of Zurich, Zurich.
M GuckenbergerDepartment of Radiation Oncology, University Hospital of Zurich, Zurich.
M FrühDepartment of Medical Oncology/Hematology, Cantonal Hospital of St. Gallen, St. Gallen; University of Bern, Bern.
D C BetticherClinics of Medical Oncology, Cantonal Hospital of Fribourg (HFR), Fribourg.
H-B RisClinics for Thoracic Surgery, Hôpital du Valais, Sion, Switzerland.
R StuppLurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, USA; Department of Medical Oncology, Centre Hospitalier Universitaire Vaudois (CHUV) and University of Lausanne, Lausanne.
S I RothschildDepartment of Medical Oncology, University Hospital Basel, Basel; Department of Medical Oncology/Hematology, Cantonal Hospital Baden, Baden.
L BubendorfInstitute of Pathology and Medical Genetics, University Hospital Basel, Basel.
M PlessDepartment of Medical Oncology, Cantonal Hospital Winterthur, Winterthur, Switzerland.
University Hospital of Basel · CHSwiss Group For Clinical Cancer Research · CHFribourg Development Agency · CHUniversity Hospital of Geneva · CHUniversity Hospital of Zurich · CHUniversity of Bern · CHHôpital du Valais · CHKantonsspital Graubünden · CHKantonsspital Winterthur · CHNorthwestern University · USUniversity Hospital of Bern · CHUniversity Hospital of Lausanne · CHUniversity of St.Gallen · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe inclusion of immune checkpoint inhibitors (ICIs) in the treatment of operable stage III non-small-cell lung cancer is becoming a new standard. Programmed death-ligand 1 (PD-L1) protein expression on tumor cells has emerged as the most important biomarker for sensitivity to ICIs targeting the programmed cell death protein 1 (PD-1)-PD-L1 axis. Little is known about the impact of neoadjuvant treatment on PD-L1 expression. PATIENTS AND

methodsWe assessed PD-L1 expression by immunohistochemistry (Ventana SP263 assay) on tumor cells in treatment-naive diagnostic tumor samples and matched lung resections from patients with stage III non-small-cell lung cancer included in the Swiss Group for Clinical Cancer Research (SAKK) trials 16/96, 16/00, 16/01, and 16/14. All patients received neoadjuvant chemotherapy (CT) with cisplatin/docetaxel, either as single modality (CT), with sequential radiotherapy [chemoradiation therapy (CRT)] or with the PD-L1 inhibitor durvalumab (CT + ICI).

resultsOverall, 132 paired tumor samples were analyzed from patients with neoadjuvant CT (n = 69), CRT (n = 33) and CT + ICI (n = 30). For CT and CRT, PD-L1 expression before and after neoadjuvant treatment did not differ significantly (Wilcoxon test, P = 0.94). Likewise, no statistically significant difference was observed between CT and CRT for PD-L1 expression after neoadjuvant treatment (P = 0.97). For CT + ICI, PD-L1 expression before and after neoadjuvant treatment also did not differ significantly (Wilcoxon test, P > 0.99). Event-free survival and overall survival for patients with downregulation or upregulation of PD-L1 expression after neoadjuvant treatment were similar.

conclusionsIn our cohort of patients neoadjuvant treatment did not influence PD-L1 expression, irrespective of the specific neoadjuvant treatment protocol. Dynamic change of PD-L1 expression did not correlate with event-free survival or overall survival.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsB7-H1 AntigenHumansNeoadjuvant TherapyRetrospective StudiesB7-H1 AntigenCD274 protein, humanchemoradiationimmune checkpoint inhibitornon-small-cell lung cancerPD-L1 expressionpredictive biomarker

Identifiers

PMID37441877
PMCPMC10515281
OpenAlexW4383892470

What OpenQuestion holds

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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.