Evidence map›Paper›PMID 37922690›Full record

ArticleESMO open2023

Long term activity of vemurafenib in cancers with BRAF mutations: the ACSE basket study for advanced cancers other than BRAF

J Y Blay, C Cropet, S Mansard, Y Loriot, C De La Fouchardière, J Haroche, D Topart, D Tougeron, B You, A Italiano and 21 more

Open access · goldAbstract read
In one paragraph

Article in ESMO open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% of its field
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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. UnravelingCancer drug resistance (Alhambra, Calif.) · 2025
    Article
  9. 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

31 authors at 20 institutions in 3 countries.

J Y BlayDepartment of Medicine, CentreLeon bErard, Lyon. Electronic address: jean-yves.blay@lyon.unicancer.fr.
C CropetDRCI, Centre Leon Berard, Lyon.
S MansardDermatology Department, Hôpital Estaing, University Hospital of Clermont Ferrand, Clermont-Ferrand.
Y LoriotDepartment of Medicine, Gustave Roussy, Villejuif.
C De La FouchardièreDRCI, Centre Leon Berard, Lyon.
J HarocheDepartment of Internal Medicine, Institut E3M, French Reference Centre for Histiocytosis, Pitié-Salpȇtrière, Assistance Publique-Hôpitaux de Paris, Sorbonne Université, Paris.
D TopartOnco-urology Department, Hôpital Saint ELOI, Montpellier.
D TougeronGastroenterology and Hepatology Department, Poitiers University Hospital and Faculty of Medicine of Poitiers, Poitiers.
B YouCentre d'Investigation des Thérapeutiques en Oncologie et Hématologie de Lyon (CITOHL), Hospices Civils de Lyon (IC-HCL), EA 3738 CICLY, Lyon.
A ItalianoDepartment of Medicine, Institut Bergonié, Bordeaux; Faculty of Medicine, University of Bordeaux, Bordeaux.
V Le Brun-LyDepartment of Medicine, CHU Limoges, Medical Oncology, Limoges.
J M FerreroDepartment of Medicine, Centre A. Lacassagne, Nice.
N PenelDepartment of Medical Oncology, Centre Oscar Lambret, Lille; Université de Lille, CHU Lille, ULR 2694 - METRICS: Évaluation des technologies de santé et des pratiques médicales, Lille.
M FabbroDepartment of Medicine, Institut de Cancerologie de Montpellier, Montpellier.
X TroussardDepartment of Oncology, CHU Caen, Caen.
D MalkaDepartment of Medical Oncology, Institut Mutualiste Montsouris, Paris.
I Ray-CoquardDepartment of Medicine, CentreLeon bErard, Lyon.
S LeboulleuxDepartment of Medicine, Gustave Roussy, Villejuif.
A FléchonDRCI, Centre Leon Berard, Lyon.
E MaubecAssistance Publique-Hôpitaux de Paris, Department of Dermatology, Hôpital Avicenne, Bobigny; University Sorbonne Paris Nord - Campus de Bobigny, Bobigny and UMR 1124, Campus Saint-Germain-des-Prés, Paris.
J CharlesDermatology, Allergology & Photobiology Department, CHU Grenoble Alpes, Grenoble; Institute for Advanced Biosciences, INSERM U1209, CNRS UMR5309, Université Grenoble Alpes, La Tronche.
S DalleDepartment of Dermatology, Hospices Civils de Lyon, CRCL, Université Claude Bernard Lyon1, Lyon.
S TaiebDepartment of Medical Oncology, Centre Oscar Lambret, Lille.
G C T E GarciaDepartment of Medicine, Gustave Roussy, Villejuif.
A M MandacheDRCI, Centre Leon Berard, Lyon.
N ColignonDepartment of Radiology, Saint-Antoine Hospital, Assistance Publique-Hôpitaux de Paris, Sorbonne Université, Paris.
M GavrelDepartment of Medicine, Gustave Roussy, Villejuif.
F NowakInstitut National Du Cancer, Boulogne-Billancourt.
N Hoog LabouretInstitut National Du Cancer, Boulogne-Billancourt.
C Mahier Aït OukhatarDepartment Unicancer R&D, Unicancer, Paris.
C Gomez-RocaInstitut Claudius Regaud/Institut Universitaire du Cancer de Toulouse (IUCT-Oncopole), Clinical Research Unit, Toulouse, France.
Centre Léon Bérard · FRInstitut Gustave Roussy · FRInstitut National du Cancer · FRSorbonne Université · FRCentre Antoine Lacassagne · FRCentre Hospitalier Universitaire de Caen Normandie · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Hospitalier Universitaire de Limoges · FRCentre National de la Recherche Scientifique · FRCentre Oscar Lambret · FRHôpital Saint Eloi · FRHospices Civils de Lyon · FRInstitut Claudius Regaud · FRInstitut de Recherche en Cancérologie de Montpellier · FRInstitute Mutualiste Montsouris · FRUniCancer Group · FRUniversité Claude Bernard Lyon 1 · FRUniversité de Bordeaux · FRUniversité de Lille · FRUniversité de Poitiers · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBRAF inhibitors are approved in BRAF PATIENTS AND

methodsPatients with advanced tumours other than BRAF

resultsA total of 98 advanced patients with various solid or haematological cancers, 88 with BRAF

conclusionResponses and prolonged PFS were observed in many tumours with BRAF mutations, including HCL, ECD, ovarian carcinoma, gliomas, ganglioglioma, and sarcomas. Although not all cancer types responded, vemurafenib is an agnostic oncogene therapy of cancers.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsMelanomaSarcomaBayes TheoremDisease-Free SurvivalHumansMutationProto-Oncogene Proteins B-rafSulfonamidesTreatment OutcomeVemurafenibBRAF protein, humanProto-Oncogene Proteins B-rafSulfonamidesVemurafenibBRAF(V600) mutationsefficacyobjective response rateoverall survivalprogression-free survivalsafetyvemurafenib

Identifiers

PMID37922690
PMCPMC10774964
OpenAlexW4388165176

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.