Evidence map›Paper›PMID 40025432›Full record

ArticleBMC medical research methodology2025

Addressing challenges with Matching-Adjusted Indirect Comparisons to demonstrate the comparative effectiveness of entrectinib in metastatic ROS-1 positive Non-Small Cell Lung Cancer.

Cyril Esnault, Louise Baschet, Vanessa Barbet, Gaëlle Chenuc, Maurice Pérol, Katia Thokagevistk, David Pau, Matthias Monnereau, Lise Bosquet, Thomas Filleron

Registry-linked trialAbstract readComparative Study
In one paragraph

Article in BMC medical research methodology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03848052 (Epidemiological Strategy and Medical Economic), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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.

NCT03848052 recruitingnot on this map

Epidemiological Strategy and Medical Economic (ESME) Research Program / Academic Real World Data Platform: Evolution of the Therapeutic Care in Lung Cancer in France Since 2015

TypeobservationalSponsorUNICANCERRan2017 to 2026Enrolled75,000ConditionsLung Cancer
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Cyril EsnaultRoche SAS, Boulogne-Billancourt, France.
Louise BaschetHoriana, Bordeaux, France. louise.baschet@horiana.com.
Vanessa BarbetHoriana, Bordeaux, France.
Gaëlle ChenucBiometry Department, IQVIA, Bordeaux, France.
Maurice PérolMedical Oncology Department, Centre Léon Bérard, Lyon, France.
Katia ThokagevistkRoche SAS, Boulogne-Billancourt, France.
David PauRoche SAS, Boulogne-Billancourt, France.
Matthias MonnereauHoriana, Bordeaux, France.
Lise BosquetHealth Data and Partnership Department, Unicancer, Paris, France.
Thomas FilleronBiostatistics & Health Data Science Unit, Institut Claudius Régaud IUCT-O, Toulouse, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMatching Adjusted Indirect Comparison (MAIC) is a statistical method used to adjust for potential biases when comparing treatment effects between separate data sources, with aggregate data in one arm, and individual patients data in the other. However, acceptance of MAIC in health technology assessment (HTA) is challenging because of the numerous biases that can affect the estimates of treatment effects - especially with small sample sizes, increasing the risk of convergence issues. We suggest statistical approaches to address some of the challenges in supporting evidence from MAICs, applied to a case study.

methodsThe proposed approaches were illustrated with a case study comparing an integrated analysis of three single-arm trials of entrectinib with the French standard of care using the Epidemio-Strategy and Medical Economics (ESME) Lung Cancer Data Platform, in metastatic ROS1-positive Non-Small Cell Lung Cancer (NSCLC) patients. To obtain convergent models with balanced treatment arms, a transparent predefined workflow for variable selection in the propensity score model, with multiple imputation of missing data, was used. To assess robustness, multiple sensitivity analyses were conducted, including Quantitative Bias Analyses (QBA) for unmeasured confounders (E-value, bias plot), and for missing at random assumption (tipping-point analysis).

resultsThe proposed workflow was successful in generating satisfactory models for all sub-populations, that is, without convergence problems and with effectively balanced key covariates between treatment arms. It also gave an indication of the number of models tested. Sensitivity analyses confirmed the robustness of the results, including to unmeasured confounders. The QBA performed on the missing data allowed to exclude the potential impact of the missing data on the estimate of comparative effectiveness, even though approximately half of the ECOG Performance Status data were missing.

conclusionsTo the best of our knowledge, we present the first in-depth application of QBA in the context of MAIC. Despite the real-world data limitations, with this MAIC, we show that it is possible to confirm the robustness of the results by using appropriate statistical methods.

trial registrationNA.

Indexed as

BenzamidesCarcinoma, Non-Small-Cell LungIndazolesLung NeoplasmsProtein-Tyrosine KinasesAntineoplastic AgentsHumansProto-Oncogene ProteinsTechnology Assessment, BiomedicalTreatment OutcomeAntineoplastic AgentsBenzamidesentrectinibIndazolesProtein-Tyrosine KinasesProto-Oncogene ProteinsROS1 protein, humanE-valueMAICMissing dataQBAResidual confounding

Identifiers

PMID40025432
PMCPMC11872303

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.