Evidence map›Paper›PMID 41647713›Full record

ArticleESMO real world data and digital oncology2025

Prognostic score models for acquired resistance to frontline anti-programmed cell death protein 1/programmed death-ligand 1 therapy in metastatic non-small-cell lung cancer.

J C Murray, Q Huang, Y-C Chen, C Hu, R L DiSantostefano, C Wong, L Glatz, E Curran, L C Villaruz, A N Hasan and 1 more

Abstract read
In one paragraph

Article in ESMO real world data and digital oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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.

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

J C MurraySidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, USA.
Q HuangJohnson & Johnson, New Brunswick, USA.
Y-C ChenJohnson & Johnson, New Brunswick, USA.
C HuSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, USA.
R L DiSantostefanoJohnson & Johnson, New Brunswick, USA.
C WongJohnson & Johnson, New Brunswick, USA.
L GlatzJohnson & Johnson, New Brunswick, USA.
E CurranJohnson & Johnson, New Brunswick, USA.
L C VillaruzHillman Cancer Center, University of Pittsburgh, Pittsburg, USA.
A N HasanJohnson & Johnson, New Brunswick, USA.
A J SchoenfeldMemorial Sloan Kettering Cancer Center, Weill Cornell Medical College, New York, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Acquired resistance (AR) to immunotherapy following initial response occurs frequently in metastatic non-small-cell lung cancer (mNSCLC). We developed and validated easy-to-apply prognostic score models to identify patients with mNSCLC at greater risk of AR to frontline (1L) anti-programmed cell death protein 1/programmed death-ligand 1 [anti-PD-(L)1] therapy. Materials and methods: Electronic health records of patients with mNSCLC who responded to 1L anti-PD-(L)1 (diagnosed 2015-2023) in the ConcertAI Patient360™ database were analyzed. Multivariable Cox models (monotherapy versus combination) assessing association between baseline prognostic factors and real-world duration of response (rwDoR) were used to develop prognostic scores and stratify patients into low- and high-risk groups. Risk stratification was evaluated using Kaplan-Meier curves, performance metrics, and decision curves. External validation utilized the COTA NSCLC dataset. Results: The majority of patients ( Conclusions: Proposed prognostic score models may facilitate identifying patient subsets at higher risk of AR to 1L anti-PD-(L)1.

Indexed as

acquired resistanceduration of responsemetastatic non-small-cell lung cancerPD-(L)1prognostic model

Identifiers

PMID41647713
PMCPMC12836523

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