Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.
0numbers the graph read from it
0cells of the map it votes in
10citing 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.
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
10 citing papers in PubMed, 1 synthesis or guideline pooled it.
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
92 authors.
Audrey-Anne LamoureuxDepartment of Neurosciences, University of Montreal, CHU Sainte-Justine, Montreal, Quebec, Canada.ORCID 0009-0008-3878-8995
Michael J FisherDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0003-3408-3839
Lauriane LemelleSIREDO Oncology Center (Care, Innovation and Research for Children and AYA with Cancer), PSL Research University, Institut Curie, Paris, France.ORCID 0000-0002-3333-5048
Elke PfaffDivision of Pediatric Glioma Research, Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany.ORCID 0000-0002-3967-2264
Pouneh Amir-YazdaniDepartment of Neurosciences, University of Montreal, CHU Sainte-Justine, Montreal, Quebec, Canada.ORCID 0000-0001-8403-7131
Christof KrammDivision of Pediatric Hematology and Oncology, University Medical Center Göttingen, Göttingen, Germany.ORCID 0000-0002-5017-926X
Bernarda KazanowskaDepartment of Pediatric Hematology/Oncology and BMT, Wroclaw Medical University, Wroclaw, Poland.
Caroline HutterDepartment of Pediatrics, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.ORCID 0000-0003-2059-4814
Stefan M PfisterDivision of Pediatric Glioma Research, Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany.ORCID 0000-0002-5447-5322
Dominik SturmDivision of Pediatric Glioma Research, Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany.ORCID 0000-0003-0250-1696
David T W JonesDivision of Pediatric Glioma Research, Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany.ORCID 0000-0002-2036-5141
Daniel OrbachSIREDO Oncology Center (Care, Innovation and Research for Children and AYA with Cancer), PSL Research University, Institut Curie, Paris, France.ORCID 0000-0002-2520-139X
Gaëlle PierronSIREDO Oncology Center (Care, Innovation and Research for Children and AYA with Cancer), PSL Research University, Institut Curie, Paris, France.ORCID 0000-0002-2536-7680
Scott RaskinDepartment of Pediatrics, University of Cincinnati Medical School, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.ORCID 0000-0003-1160-9842
Alexander DrilonMemorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, New York.ORCID 0000-0001-6806-9061
Eli L DiamondMemorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, New York.ORCID 0000-0001-5456-5961
Guilherme HaradaMemorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, New York.ORCID 0000-0003-4012-3251
Michal ZapotockyDepartment of Paediatric Haematology and Oncology, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.ORCID 0000-0002-9013-2546
Josef ZamecnikDepartment of Pathology and Molecular Medicine, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.ORCID 0000-0001-8697-9632
Lenka KrskovaDepartment of Pathology and Molecular Medicine, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.ORCID 0000-0002-6113-6310
Benjamin EllezamDepartment of Neurosciences, University of Montreal, CHU Sainte-Justine, Montreal, Quebec, Canada.ORCID 0000-0002-8716-7924
Alexander G WeilDepartment of Neurosciences, University of Montreal, CHU Sainte-Justine, Montreal, Quebec, Canada.ORCID 0000-0003-4162-6096
Dominic VenneDepartment of Neurosciences, University of Montreal, CHU Sainte-Justine, Montreal, Quebec, Canada.ORCID 0000-0003-3978-3738
Pierre LeblondInstitut d'Hématologie et d'Oncologie Pédiatrique and Pluridisciplinar Research in Pediatric Oncology for Perspectives in Evaluation Care and Therapy (PROSPECT), Centre Leon Berard, Lyon, France.ORCID 0000-0002-7088-2614
Hallie ColtinDivision of Pediatric Hematology-Oncology, University of Montreal, CHU Sainte-Justine, Montreal, Quebec, Canada.ORCID 0000-0003-0820-6276
Nicholas G GottardoDepartment of Pediatric Oncology and Hematology, Perth Children's Hospital, Perth, Western Australia, Australia.ORCID 0000-0002-1082-6776
Hetal DholariaDepartment of Pediatric Oncology and Hematology, Perth Children's Hospital, Perth, Western Australia, Australia.ORCID 0000-0003-1713-3822
Dorte Schou NørøxeDepartment of Oncology, DCCC-Brain Tumor Center, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0001-9921-8277
Chantel CacciottiDivision of Hematology/Oncology, Department of Pediatrics, London Health Sciences Centre and Western University, London, Ontario, Canada.ORCID 0000-0002-4968-8956
Maura MassiminoFondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0002-5506-2001
Elisabetta SchiavelloFondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0002-8049-7445
François DozSIREDO Oncology Center (Care, Innovation and Research for Children and AYA with Cancer), PSL Research University, Institut Curie, Paris, France.ORCID 0000-0001-9286-4831
Theodore W LaetschDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0002-8497-3138
Sébastien PerreaultDepartment of Neurosciences, University of Montreal, CHU Sainte-Justine, Montreal, Quebec, Canada.ORCID 0000-0002-4417-7698
Funding
X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Integration of Imaging and Circulating Plasma Cell-Free DNA Sequencing Using MSK-ACCESS to Monitor Treatment Response and Predict Progression in Patients With Multiple Cancers on Targeted TherapyR01CA273224 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Michael F. Berger, Alexander Drilon · 2022 to 2026
$3.6M
Molecular Pathogenesis and Therapy of Systemic Histiocytic NeoplasmsR37CA259260 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Eli Lous Diamond · 2021 to 2026
$3.3M
National Cancer Institute (NCI) 1R01CA251591001A1NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA273224NCI NIH HHS R37 CA259260
6 · The paper itself
Abstract
purposeTropomyosin receptor kinase (TRK) fusions are detected in less than 2% of central nervous system tumors. There are limited data on the clinical course of affected patients. EXPERIMENTAL
designWe conducted an international retrospective cohort study of patients with TRK fusion-driven central nervous system tumors.
resultsA total of 119 patients were identified. The median age at the time of diagnosis was 4.5 years. The majority were reported to have a histology consistent with a diagnosis of high-grade glioma (HGG; 57.1%) followed by low-grade glioma (LGG; 27.7%). Pediatric patients had a better prognosis, with a median overall survival of 185.5 months compared with 24.8 months in adults (P < 0.0001). Patients with LGG also had a better outcome when compared with HGG (P = 0.0012). The objective response was 68.8% with larotrectinib compared with 38.1% for nontargeted treatment.
conclusionsChildren with LGG had a favorable outcome compared with adult glioma and HGG. TRK inhibitors seem to improve tumor control.
Indexed as
Central Nervous System NeoplasmsGene FusionGliomaOncogene Proteins, FusionReceptor, trkAAdolescentAdultAgedChildChild, PreschoolFemaleHumansInfantMaleMiddle AgedPrognosislarotrectinibOncogene Proteins, FusionProtein Kinase InhibitorsPyrazolesPyrimidinesReceptor, trkAReceptor, trkB
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.
Clinical Characteristics and Outcomes of Central Nervous System Tumors Harboring NTRK Gene Fusions. · full record | OpenQuestion