Evidence map›Paper›PMID 41699769›Full record

SynthesisCPT: pharmacometrics & systems pharmacology2026

Model-Based Meta-Analysis of Overall Survival in Vulnerable Platinum-Ineligible NSCLC Populations.

Joseph Chen, Russ Wada, Nancy Zhang, Vilma Graupner, Stefanie Morris, Youyou Hu, Wei Zhang, Nastya Kassir, Benjamin Wu, Phyllis Chan

Registry-linked trialAbstract readMeta-Analysis
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. It is linked to trial NCT03191786 (A Phase III, Open-Label, Multicenter, Randomized Study to Investigate the Efficacy and Safety of Atezolizumab Compared With Chemotherapy in Patients With Treatment Naïve Advanced or Recurrent), which is not on this map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

NCT03191786 phase3completednot on this map

A Phase III, Open-Label, Multicenter, Randomized Study to Investigate the Efficacy and Safety of Atezolizumab Compared With Chemotherapy in Patients With Treatment Naïve Advanced or Recurrent (Stage IIIb Not Amenable for Multimodality Treatment) or Metastatic (Stage IV) Non-Small Cell Lung Cancer Who Are Deemed Unsuitable for Platinum-Containing Therapy

TypeinterventionalSponsorHoffmann-La RocheRan2017 to 2023Enrolled453ConditionsNon-Small Cell Lung CancerArmsAtezolizumab (MPDL3280A), an engineered anti-PD-L1 antibody, Vinorelbine, Gemcitabine
3 · Its place in the literature

Who cites it

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

  1. Pooled it
  2. Article
  3. 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

10 authors.

Joseph ChenGenentech/Roche, South San Francisco, California, USA.ORCID https://orcid.org/0000-0002-5998-7765
Russ WadaQuanTx, Mountain View, California, USA.
Nancy ZhangQuanTx, Mountain View, California, USA.
Vilma GraupnerRoche, Basel, Switzerland.
Stefanie MorrisRoche, Basel, Switzerland.
Youyou HuRoche, Basel, Switzerland.
Wei ZhangGenentech/Roche, South San Francisco, California, USA.
Nastya KassirGenentech/Roche, South San Francisco, California, USA.ORCID https://orcid.org/0000-0001-6193-2993
Benjamin WuGenentech/Roche, South San Francisco, California, USA.ORCID https://orcid.org/0000-0001-6443-3671
Phyllis ChanGenentech/Roche, South San Francisco, California, USA.ORCID https://orcid.org/0000-0003-1509-1526

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IPSOS (NCT03191786) is a Phase III trial comparing atezolizumab (atezo) monotherapy to single-agent chemotherapy (gemcitabine or vinorelbine) in patients with treatment-naïve locally advanced or metastatic NSCLC unsuitable for platinum-doublet chemotherapy. The study demonstrated significant overall survival (OS) improvement in the atezo arm compared to single-agent chemotherapy, with a stratified hazard ratio (HR) of 0.78 (95% CI: 0.63-0.97; p = 0.028). Since the IPSOS control arm only allowed gemcitabine or vinorelbine, a model-based meta-analysis (MBMA) was conducted, extracting OS data from published literature in similar patients, adjusting for population differences across trials, to estimate the HR between IPSOS arms versus historical trials which utilized single-agent chemotherapies. The aim was to demonstrate the non-inferiority of the IPSOS control arm versus historical controls. The literature search included patients who were chemotherapy-naïve, had advanced or metastatic NSCLC, were platinum-ineligible, ≥ 70 years or had ECOG ≥ 2, and were treated with single-agent paclitaxel, docetaxel, gemcitabine, pemetrexed, or vinorelbine. Summary-level OS data were extracted by digitizing Kaplan-Meier curves, resulting in a database of 26 trials with 41 arms and 3637 participants. A nonparametric approach modeling the conditional probability of OS data was implemented. After adjusting for ECOG PS (the only significant covariate), the model-predicted HR for the IPSOS control arm relative to historical trials was 0.543 (95% CI: 0.435-0.677), and the HR for the IPSOS atezo monotherapy arm was 0.418 (95% CI: 0.335-0.522). Overall, the MBMA results support the benefit of atezo seen in the IPSOS trial.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic AgentsCarcinoma, Non-Small-Cell LungLung NeoplasmsClinical Trials, Phase III as TopicDeoxycytidineGemcitabineHumansPlatinumVinblastineVinorelbineAntibodies, Monoclonal, HumanizedAntineoplastic AgentsatezolizumabDeoxycytidineGemcitabinePlatinumVinblastineVinorelbine

Identifiers

PMID41699769
PMCPMC12909276

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Registered trials

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.