Evidence map›Paper›PMID 40080277›Full record

ArticleTargeted oncology2025

Compassionate Access to Brigatinib for Patients with Non-small-cell Lung Cancer Harboring a ROS1 Rearrangement: Results from the BRIGAROS Study.

Jean Mourlanette, Gaelle Rousseau-Bussac, Siham Mallah, Florian Guisier, Gerard Zalcman, Rémi Veillon, Clarisse Audigier-Valette, Magali Roa, Isabelle Nicolle, Helene Doubre and 12 more

Abstract readMulticenter Study
In one paragraph

Article in Targeted 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.

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.

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

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

22 authors.

Jean MourlanettePulmonology Department, Hôpital Larrey, CHU Toulouse, Chemin de Pouvourville, 31400, Toulouse, France.ORCID http://orcid.org/0009-0003-0057-7424
Gaelle Rousseau-BussacCH Intercommunal de Créteil, Créteil, France.
Siham MallahPulmonology Department, Hôpital Larrey, CHU Toulouse, Chemin de Pouvourville, 31400, Toulouse, France.
Florian GuisierCentre Hospitalier Universitaire Charles Nicolle, Rouen, France.
Gerard ZalcmanCentre Hospitalier Universitaire Bichat, Paris, France.
Rémi VeillonCentre Hospitalier Universitaire Haut Leveque, Bordeaux, France.
Clarisse Audigier-ValetteCentre Hospitalier Sainte Musse, Toulon, France.
Magali RoaCentre Hospitalier Intercommunal de Fréjus Saint Raphael, Fréjus, France.
Isabelle NicolleCentre Hospitalier de Grasse, Grasse, France.
Helene DoubreCentre Hospitalier Foch, Paris, France.
Nicolas CloarecCentre Hospitalier d'Avignon, Avignon, France.
Régine LamyGroupe Hospitalier Bretagne Sud-Lorient, Lorient, France.
Hugues MorelCentre Hospitalier Régional d'Orléans, Orléans, France.
Hubert CurcioCRLCC François Baclesse, Caen, France.
Aurélie LagrangeCentre Georges Francois Leclerc, Dijon, France.
Roland SchottInstitut de Cancérologie Strasbourg Europe, Strasbourg, France.
Marielle SabatiniCentre Hospitalier de Bayonne, Bayonne, France.
Anne Claire ToffartCentre Hospitalier Universitaire de Grenoble, Grenoble, France.
Julian PinsolleCentre Hospitalier de Chambéry, Chambéry, France.
Jaafar BennounaCentre Hospitalier Universitaire de Nantes, Nantes, France.
Christos ChouaidCH Intercommunal de Créteil, Créteil, France.
Julien MazieresPulmonology Department, Hôpital Larrey, CHU Toulouse, Chemin de Pouvourville, 31400, Toulouse, France. mazieres.j@chu-toulouse.fr.ORCID http://orcid.org/0000-0002-5921-7613

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundROS1 chromosomic rearrangement is a rare oncogenic driver, and patients with this rearrangement benefit from specific targeted treatments in the first-line setting. However, therapeutic options are limited in pretreated patients. Brigatinib is a validated drug for ALK rearrangements, and also has an in vitro activity against ROS1. In vivo efficacy is also suggested in some clinical series.

objectiveWe aimed to specifically study brigatinib in patients with pretreated advanced non-small-cell lung cancer (NSCLC).

methodsWe retrospectively collected data from 20 centers in France. Brigatinib was delivered through a compassionate use program in France between 2018 and 2020. The primary endpoint was progression-free survival. Secondary endpoints were the objective response rate, overall survival, and tolerance.

resultsTwenty-five patients treated with brigatinib were included in our study. All patients were pretreated, and all of them previously received crizotinib. Median progression-free survival was 3.8 months (95% confidence interval 2.8-7.1). The objective response rate was 32%, with a disease control rate of 48%. Three patients had a prolonged response of more than 18 months at the end of data collection. We did not identify factors predictive of prolonged response. There were no grade 4 or 5 toxicities.

conclusionBrigatinib may represent an interesting therapeutic option for patients who have progressed after standard treatments.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsOrganophosphorus CompoundsProtein-Tyrosine KinasesProto-Oncogene ProteinsPyrimidinesAdultAgedAged, 80 and overCompassionate Use TrialsFemaleGene RearrangementHumansMaleMiddle AgedRetrospective StudiesbrigatinibOrganophosphorus CompoundsProtein-Tyrosine KinasesProto-Oncogene ProteinsPyrimidinesROS1 protein, human

Identifiers

PMID40080277
PMCPMC11933156

What OpenQuestion holds

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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.