Evidence map›Paper›PMID 34850167›Full record

Trial reportNeuro-oncology2022

Efficacy and safety of larotrectinib in TRK fusion-positive primary central nervous system tumors.

François Doz, Cornelis M van Tilburg, Birgit Geoerger, Martin Højgaard, Ingrid Øra, Valentina Boni, Michael Capra, Julia Chisholm, Hyun Cheol Chung, Steven G DuBois and 20 more

2 registry-linked trialsOpen access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Neuro-oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 110 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed, 3 pooled it
14.9field-weighted citation impact, top 1% 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.

NCT02576431 phase2completednot on this map

A Study to Learn How Well the Drug Larotrectinib Works in Adults With Different Solid Cancers With a Change in the Genes Called NTRK Fusion

TypeinterventionalSponsorBayerRan2015 to 2025Enrolled215ConditionsSolid Tumors Harboring NTRK FusionArmsBAY2757556 (Larotrectinib, Vitrakvi)
NCT02637687 phase1 / phase2active not recruitingnot on this map

A Phase 1/2 Study of the Oral TRK Inhibitor Larotrectinib in Pediatric Patients With Advanced Solid or Primary Central Nervous System Tumors

TypeinterventionalSponsorBayerRan2015 to 2026Enrolled154ConditionsSolid Tumors Harboring NTRK FusionArmsLarotrectinib (Vitrakvi, BAY2757556)
3 · Its place in the literature

Who cites it

110 citing papers in PubMed, 3 syntheses or guidelines pooled it, 160 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Review
  6. Review
  7. Obstacles and Trials in Treating Primary Brain Tumors.International journal of molecular sciences · 2026
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. TRK inhibitors in pediatric gliomas.Neuro-oncology advances · 2026
    Review
  14. Article
  15. Recent Advances in Targeted Therapies for Adult Gliomas.Current neurology and neuroscience reports · 2026
    Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. Review

50 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors at 20 institutions in 14 countries.

François DozSIREDO Oncology Center (Care, Innovation and Research for Children and AYA with Cancer), Institut Curie and Université de Paris, Paris, France.
Cornelis M van TilburgHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg University Hospital and German Cancer Research Center (DKFZ), Heidelberg, Germany.
Birgit GeoergerGustave Roussy Cancer Center, Department of Pediatric and Adolescent Oncology, Université Paris-Saclay, INSERM U1015, Villejuif, France.
Martin HøjgaardDepartment of Oncology, Righospitalet , Copenhagen, Denmark.
Ingrid ØraDepartment of Pediatric Oncology, Skåne University Hospital, Lund & Karolinska University Hospital, Stockholm, Sweden.
Valentina BoniSTART Madrid CIOCC, HM Hospital Universitario Sanchinarro, Madrid, Spain.
Michael CapraPaediatric Oncology, Children's Health Ireland, Crumlin, Dublin, Ireland.
Julia ChisholmChildren and Young People's Unit, Royal Marsden Hospital, Surrey, UK.
Hyun Cheol ChungYonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea.
Steven G DuBoisDepartment of Pediatrics, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts, USA.
Soledad Gallego-MelconVall d'Hebron Children's Hospital, Barcelona, Spain.
Nicolas U GerberDepartment of Oncology, University Children's Hospital, Zurich, Switzerland.
Hiroaki GotoDivision of Hematology/Oncology, Kanagawa Children's Medical Center, Yokohama, Japan.ORCID 0000-0001-6737-1509
Juneko E Grilley-OlsonLineberger Cancer Center, University of North Carolina Hospitals, Chapel Hill, North Carolina, USA.
Jordan R HansfordRoyal Children's Hospital Melbourne, Murdoch Children's Research Institute, University of Melbourne, Melbourne, Australia.
David S HongDepartment of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Antoine ItalianoDepartment of Medical Oncology, Institute Bergonie, Bordeaux, France.
Hyoung Jin KangDepartment of Pediatrics, Cancer Research Institute, Seoul National University College of Medicine, Seoul, South Korea.
Karsten NysomDepartment of Pediatrics and Adolescent Medicine, University Hospital Rigshospitalet, Copenhagen, Denmark.
Anne ThorwarthDepartment of Pediatric Oncology/Hematology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Joanna StefanowiczDepartment of Paediatrics, Hematology and Oncology, Faculty of Medicine, Medical University of Gdansk, Gdansk, Poland.
Makoto TaharaDepartment of Head and Neck Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID 0000-0001-9035-3106
David S ZieglerKids Cancer Centre, Sydney Children's Hospital, Randwick, Australia.
Igor T GavrilovicDepartment of Neurology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Ricarda NorenbergChrestos Concept GmbH & Co. KG, Essen, Germany.
Laura DimaBayer Consumer Care AG, Basel, Switzerland.
Esther De La CuestaBayer HealthCare Pharmaceuticals, Whippany, New Jersey, USA.
Theodore W LaetschDepartment of Pediatrics and Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center/Children's Health, Dallas, Texas, USA.
Alexander DrilonDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA (A.D.); Department of Medicine, Weill Cornell Medical College, New York, New York, USA.ORCID 0000-0001-6806-9061
Sebastien PerreaultDepartment of Neurosciences, CHU Sainte Justine, Montreal, Quebec, Canada.
Memorial Sloan Kettering Cancer Center · USRigshospitalet · DKBayer (Switzerland) · CHBayer (United States) · USCentre Hospitalier Universitaire Sainte-Justine · CACharité - Universitätsmedizin Berlin · DEChildren's Health Ireland at Crumlin · IEDana-Farber/Boston Children's Cancer and Blood Disorders Center · USGdańsk Medical University · PLGerman Cancer Research Center · DEHospital Universitario HM Sanchinarro · ESInserm · FRInstitut Bergonié · FRKanagawa Children's Medical Center · JPKarolinska University Hospital · SENational Cancer Center Hospital East · JPRoyal Children's Hospital · AURoyal Marsden Hospital · GBSeoul National University Hospital · KRThe University of Texas MD Anderson Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Department of HealthNCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundLarotrectinib is a first-in-class, highly selective tropomyosin receptor kinase (TRK) inhibitor approved to treat adult and pediatric patients with TRK fusion-positive cancer. The aim of this study was to evaluate the efficacy and safety of larotrectinib in patients with TRK fusion-positive primary central nervous system (CNS) tumors.

methodsPatients with TRK fusion-positive primary CNS tumors from two clinical trials (NCT02637687, NCT02576431) were identified. The primary endpoint was investigator-assessed objective response rate (ORR).

resultsAs of July 2020, 33 patients with TRK fusion-positive CNS tumors were identified (median age: 8.9 years; range: 1.3-79.0). The most common histologies were high-grade glioma (HGG; n = 19) and low-grade glioma (LGG; n = 8). ORR was 30% (95% confidence interval [CI]: 16-49) for all patients. The 24-week disease control rate was 73% (95% CI: 54-87). Twenty-three of 28 patients (82%) with measurable disease had tumor shrinkage. The 12-month rates for duration of response, progression-free survival, and overall survival were 75% (95% CI: 45-100), 56% (95% CI: 38-74), and 85% (95% CI: 71-99), respectively. Median time to response was 1.9 months (range 1.0-3.8 months). Duration of treatment ranged from 1.2-31.3+ months. Treatment-related adverse events were reported for 20 patients, with grade 3-4 in 3 patients. No new safety signals were identified.

conclusionsIn patients with TRK fusion-positive CNS tumors, larotrectinib demonstrated rapid and durable responses, high disease control rate, and a favorable safety profile.

Indexed as

Antineoplastic AgentsGliomaNeoplasmsAdultChildHumansOncogene Proteins, FusionProtein Kinase InhibitorsPyrazolesPyrimidinesAntineoplastic AgentslarotrectinibOncogene Proteins, FusionProtein Kinase InhibitorsPyrazolesPyrimidineslarotrectinibNTRK gene fusionsprimary CNS tumorsTRK fusion

Identifiers

PMID34850167
PMCPMC9159442
OpenAlexW3215197047

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.