Evidence map›Paper›PMID 41709716›Full record

SynthesisCPT: pharmacometrics & systems pharmacology2026

Model-Based Meta-Analysis of Objective Response Rate and Survival Endpoints to Compare PD-1 and PD-L1 Treatment Outcomes in Non-Small Cell Lung Cancer.

Richard C Franzese, Li Qin, Shuai Fu, Benjamin Rich, Eleftherios Zografos, Matthew L Zierhut, Sandra A G Visser

Abstract readMeta-AnalysisComparative Study
In one paragraph

Synthesis in CPT: pharmacometrics & systems pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

7 authors.

Richard C FranzeseClinical Pharmacology Modeling and Simulation, GSK, Upper Providence, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-9579-3730
Li QinCertara USA, Inc., Radnor, Pennsylvania, USA.ORCID https://orcid.org/0000-0001-5002-3372
Shuai FuCertara USA, Inc., Radnor, Pennsylvania, USA.ORCID https://orcid.org/0000-0003-1889-3030
Benjamin RichInnoMx, Outremont, Quebec, Canada.
Eleftherios ZografosClinical Pharmacology Modeling and Simulation, GSK, Upper Providence, Pennsylvania, USA.ORCID https://orcid.org/0009-0007-3389-7175
Matthew L ZierhutCertara USA, Inc., Radnor, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-5221-9157
Sandra A G VisserClinical Pharmacology Modeling and Simulation, GSK, Upper Providence, Pennsylvania, USA.ORCID https://orcid.org/0009-0008-2186-7195

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmed cell death (PD) protein (ligand [L])-1 inhibitors are established treatments for metastatic non-small cell lung cancer (mNSCLC). In oncology, progression-free survival (PFS) and objective response rate (ORR) are often used as surrogates for overall survival (OS) to inform clinical development; however, there remains uncertainty in the concordance between these endpoints. This study evaluated the impact of a broad set of PD-(L)1 inhibitors on efficacy, explored the relationship between ORR and survival endpoints, and compared PD-1 and PD-L1 treatments for mNSCLC. A dataset of 114 studies was used to conduct a sequential two-stage model-based meta-analysis (MBMA). Firstly, an MBMA with mixed-effects logistic regression was applied to evaluate treatment-specific and clinical covariate effects on ORR. Secondly, MBMAs for OS and PFS were conducted with a mixed-effects semi-parametric proportional hazard approach using digitized Kaplan-Meier curves, with the treatment type, covariates, and ORR as inputs. ORR was demonstrated to be a significant predictor of OS and PFS. Simulations of head-to-head comparisons of treatment types were conducted using these models. Trends in predicted outcomes numerically favored PD-1 over PD-L1 treatments, but differences were not statistically significant. These findings support evidence-based decision-making for late-stage trial designs using ORR data from earlier phase trials, enabling benchmarking of emerging data by adjusting for explained and unexplained sources of variability in existing and emerging data.

Indexed as

B7-H1 AntigenCarcinoma, Non-Small-Cell LungImmune Checkpoint InhibitorsLung NeoplasmsProgrammed Cell Death 1 ReceptorHumansProgression-Free SurvivalTreatment OutcomeB7-H1 AntigenCD274 protein, humanImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 Receptorcomparative effectivenessmixed effect modelsmodel based meta‐analysisoncologysurrogate endpointsurvival analysistrial simulation

Identifiers

PMID41709716
PMCPMC12917330

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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.