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Naslov:Limited predictive value of PD-L1 TPS for pathological response in NSCLC is not attributable to interobserver variability
Avtorji:ID Steinestel, Konrad (Avtor)
ID Löwer-Kiem, Lena-Maria (Avtor)
ID Ambrosi, Francesca (Avtor)
ID Becker, Anne-Sophie (Avtor)
ID Bohnenberger, Hanibal (Avtor)
ID Bräutigam, Konstantin (Avtor)
ID Cazzato, Gerardo (Avtor)
ID Conde, Esther (Avtor)
ID Cozac-Szőke, Andreea-Raluca (Avtor)
ID Curto, Daniel (Avtor)
ID Dahlberg, Jan-Olof (Avtor)
ID Gama, João Martins (Avtor)
ID Gambella, Alessandro (Avtor)
ID Hutarew, Georg (Avtor)
ID Lopez-Rios, Fernando (Avtor)
ID Lucà, Stefano (Avtor)
ID Lunardi, Francesca (Avtor)
ID Matek, Christian (Avtor)
ID Meyer, Christian (Avtor)
ID Olteanu, Gheorghe-Emilian (Avtor)
ID Popper, Helmut H. (Avtor)
ID Roden, Anja C (Avtor)
ID Samaras, Menelaos G (Avtor)
ID Skok, Kristijan (Avtor)
ID Suster, David (Avtor)
ID Weissferdt, Annikka (Avtor)
ID Zustin, Jozef (Avtor)
ID Kümpers, Christiane (Avtor)
ID Elsner, Felix (Avtor)
Datoteke:.pdf RAZ_Steinestel_Konrad_2026.pdf (2,20 MB)
MD5: 3A1E7F3368F695B3A2BCC5AEEC798C93
 
URL https://doi.org/10.1016/j.lungcan.2026.109510
 
URL https://linkinghub.elsevier.com/retrieve/pii/S0169500226005714
 
Jezik:Angleški jezik
Vrsta gradiva:Znanstveno delo
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:MF - Medicinska fakulteta
Opis:Background PD-L1 tumor proportion score (TPS) is used to guide immunotherapy in non-small cell lung cancer (NSCLC), yet its ability to predict pathological response in the neoadjuvant setting remains limited. Methods Thirty pathologists from 11 countries independently assessed PD-L1 TPS in pre-treatment biopsies and residual viable tumor (RVT) in matched resection specimens after neoadjuvant chemoimmunotherapy in 30 digitized cases from the ReGraDE (regression grading in Germany) study. Interobserver agreement was evaluated using intraclass correlation coefficients (ICC) and Fleiss’ kappa. Associations between TPS and RVT were analyzed using Pearson correlation, and correlations derived from single-rater and averaged TPS were compared using the Williams test. Results Interobserver agreement was moderate for both TPS and RVT (ICC = 0.74, 95% CI 0.60–0.87, and ICC = 0.74, 95% CI 0.62–0.85, respectively) and became near-perfect when mean scores per case were calculated across observers (ICC = 0.99, for both). However, TPS remained poorly correlated with RVT for both single-rater assessment (r = –0.17, p = 0.38) and averaged TPS (r = –0.16, p = 0.39) with no significant difference between these approaches (p = 0.96). Differences in interpretation thresholds were observed particularly in borderline cases around the 1% TPS cut-off and in distinguishing 0% from minimal RVT, but did not account for the lack of association between TPS and RVT. Systematic differences were observed depending on individual professional experience, particularly in borderline cases. Conclusion Interobserver variability does not explain the limited predictive value of PD-L1 TPS in the neoadjuvant setting, suggesting an intrinsic limitation of the biomarker.
Ključne besede:non-small cell lung cancer (NSCLC), PD-L1, tumor proportion score (TPS), residual viable tumor (RVT), neoadjuvant chemoimmunotherapy, interobserver variability
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Poslano v recenzijo:05.06.2026
Datum sprejetja članka:05.05.2026
Datum objave:01.08.2026
Založnik:Elsevier
Leto izida:2026
Št. strani:str. [1]-8
Številčenje:Letn. 218, Aug. 2026, št. članka 109510
PID:20.500.12556/DKUM-100352 Novo okno
UDK:616-006
COBISS.SI-ID:291043075 Novo okno
DOI:10.1016/j.lungcan.2026.109510 Novo okno
ISSN pri članku:1872-8332
Datum objave v DKUM:15.09.2026
Število ogledov:102
Število prenosov:0
Metapodatki:XML DC-XML DC-RDF
Področja:Ostalo
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Gradivo je del revije

Naslov:Lung cancer
Založnik:Elsevier
ISSN:1872-8332
COBISS.SI-ID:2725499 Novo okno

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Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
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