Evidence map›Paper›PMID 31151904›Full record

Trial reportThe Lancet. Oncology2019

Selumetinib in paediatric patients with BRAF-aberrant or neurofibromatosis type 1-associated recurrent, refractory, or progressive low-grade glioma: a multicentre, phase 2 trial.

Jason Fangusaro, Arzu Onar-Thomas, Tina Young Poussaint, Shengjie Wu, Azra H Ligon, Neal Lindeman, Anuradha Banerjee, Roger J Packer, Lindsay B Kilburn, Stewart Goldman and 24 more

2 registry-linked trialsOpen access · greenAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in The Lancet. Oncology, 2019. 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 319 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
319citing papers in PubMed, 2 pooled it
36.5field-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.

NCT05555550 early_phase1recruitingnot on this mapstarted 2026, after this paper: background citation

Evaluation of 18F-Fluciclovine PET-MRI as a Biomarker of Response in Pediatric and Young Adult Patients With Low Grade Gliomas (LGG)

TypeinterventionalSponsorChildren's Hospital of PhiladelphiaRan2026 to 2027Enrolled30ConditionsGlioma, Low-grade Glioma, Low Grade Glioma of Brain, Glioma, MalignantArms18F-Fluciclovine
NCT06666348 phase1 / phase2recruitingnot on this mapstarted 2026, after this paper: background citation

A Phase 1/2 Study of Mirdametinib and Vinblastine for Newly Diagnosed or Previously Untreated Patients With Pediatric Low-grade Glioma and Activation of the MAPK Pathway

TypeinterventionalSponsorSt. Justine's HospitalRan2026 to 2033Enrolled50ConditionsPediatric Low-grade GliomaArmsMirdametinib
3 · Its place in the literature

Who cites it

319 citing papers in PubMed, 2 syntheses or guidelines pooled it, 484 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. SARC031: A Phase II Trial of Selumetinib and Sirolimus for Patients with Unresectable or Metastatic Malignant Peripheral Nerve Sheath Tumors (MPNST).Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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  10. Efficacy and Safety of Trametinib Monotherapy or in Combination With Dabrafenib in PediatricJournal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Trial
  11. Trial
  12. Trial
  13. Cytotoxic activity of selinexor in BRAFActa neuropathologica communications · 2026
    Article
  14. Review
  15. Efficacy and safety of trametinib use in pediatric brain tumors in a low- to middle-income country.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Article
  16. Pediatric low-grade glial, glioneuronal and neuronal tumors: a retrospective study of 85 cases.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Article
  17. Review
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

34 authors at 19 institutions in 2 countries.

Jason FangusaroDepartment of Hematology, Oncology, and Stem Cell Transplantation, Children's Healthcare of Atlanta and Emory University, Atlanta, GA, USA. Electronic address: jfangus@emory.edu.
Arzu Onar-ThomasDepartment of Biostatistics, St Jude Children's Research Hospital, Memphis, TN, USA.
Tina Young PoussaintDepartment of Radiology, Boston Children's Hospital, Boston, MA, USA.
Shengjie WuDepartment of Biostatistics, St Jude Children's Research Hospital, Memphis, TN, USA.
Azra H LigonDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Neal LindemanDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Anuradha BanerjeeCenter for Cancer and Blood Disorders, University of California, San Francisco, San Francisco, CA, USA.
Roger J PackerDepartment of Neurology, Children's National Medical Center, Washington, DC, USA.
Lindsay B KilburnDepartment of Haematology and Oncology, Children's National Medical Center, Washington, DC, USA.
Stewart GoldmanDepartment of Haematology, Oncology, Neuro-Oncology, and Stem Cell Transplantation, Ann and Robert H Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Ian F PollackDepartment of Neurosurgery, Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
Ibrahim QaddoumiDepartment of Oncology, St Jude Children's Research Hospital, Memphis, TN, USA.
Regina I JakackiDepartment of Hematology and Oncology, Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
Paul G FisherDepartment of Neurology, Stanford University Medical Center, Palo Alto, CA, USA.
Girish DhallDepartment of Hematology and Oncology, Children's Hospital Los Angeles, Los Angeles, CA, USA.
Patricia BaxterDepartment of Hematology and Oncology, Texas Children's Hospital, Houston, TX, USA.
Susan G KreissmanDepartment of Hematology and Oncology, Duke University School of Medicine, Durham, NC, USA.
Clinton F StewartDepartment of Pharmaceutical Science, St Jude Children's Research Hospital, Memphis, TN, USA.
David T W JonesDepartment of Pediatric Glioma Research Group, Hopp Children's Cancer Center Heidelberg (KiTZ) and German Cancer Research Center (DKFZ), Heidelberg, Germany.
Stefan M PfisterDepartment of Pediatric Neuro-Oncology, Hopp Children's Cancer Center Heidelberg (KiTZ) and German Cancer Research Center (DKFZ), Heidelberg, Germany.
Gilbert VezinaDepartment of Radiology, Children's National Medical Center, Washington, DC, USA.
Jessica S SternDepartment of Radiology, Ann and Robert H Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Ashok PanigrahyDepartment of Radiology, Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
Zoltan PatayDepartment of Diagnostic Imaging, St Jude Children's Research Hospital, Memphis, TN, USA.
Benita TamraziDepartment of Radiology, Children's Hospital Los Angeles, Los Angeles, CA, USA.
Jeremy Y JonesDepartment of Radiology, Nationwide Children's Hospital, Columbus, OH, USA.
Sofia S HaqueDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
David S EnterlineDepartment of Radiology, Duke University School of Medicine, Durham, NC, USA.
Soonmee ChaDepartment of Radiology, University of California, San Francisco, San Francisco, CA, USA.
Michael J FisherDepartment of Pediatric Oncology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Laurence Austin DoyleInvestigational Drug Branch, National Cancer Institute and Cancer Therapy Evaluation Program, Bethesda, MD, USA.
Malcolm SmithClinical Investigation Branch, National Cancer Institute and Cancer Therapy Evaluation Program, Bethesda, MD, USA.
Ira J DunkelDepartment of Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Maryam FouladiDepartment of Haematology and Oncology, Cincinnati Children's Hospital, Cincinnati, OH, USA.
St. Jude Children's Research Hospital · USChildren's Hospital of Pittsburgh · USChildren's National · USChildren's Hospital of Los Angeles · USDuke University · USGerman Cancer Research Center · DEHarvard University · USLurie Children's Hospital · USMemorial Sloan Kettering Cancer Center · USNational Cancer Institute · USBoston Children's Hospital · USCenter for Cancer and Blood Disorders · USChildren's Healthcare of Atlanta · USChildren's Hospital of Philadelphia · USCincinnati Children's Hospital Medical Center · USNationwide Children's Hospital · USStanford University · USTexas Children's Hospital · USUniversity of California, San Francisco · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Pediatric Brain Tumor Consortium (PBTC)UM1CA081457 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Ira J Dunkel, Arzu Onar-Thomas · 2014 to 2026
$41.4M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA021765NCI NIH HHS UM1 CA081457
6 · The paper itself

Abstract

backgroundPaediatric low-grade glioma is the most common CNS tumour of childhood. Although overall survival is good, disease often recurs. No single universally accepted treatment exists for these patients; however, standard cytotoxic chemotherapies are generally used. We aimed to assess the activity of selumetinib, a MEK1/2 inhibitor, in these patients.

methodsThe Pediatric Brain Tumor Consortium performed a multicentre, phase 2 study in patients with paediatric low-grade glioma in 11 hospitals in the USA. Patients aged 3-21 years with a Lansky or Karnofsky performance score greater than 60 and the presence of recurrent, refractory, or progressive paediatric low-grade glioma after at least one standard therapy were eligible for inclusion. Patients were assigned to six unique strata according to histology, tumour location, NF1 status, and BRAF aberration status; herein, we report the results of strata 1 and 3. Stratum 1 comprised patients with WHO grade I pilocytic astrocytoma harbouring either one of the two most common BRAF aberrations (KIAA1549-BRAF fusion or the BRAF

findingsBetween July 25, 2013, and June 12, 2015, 25 eligible and evaluable patients were accrued to stratum 1, and between Aug 28, 2013, and June 25, 2015, 25 eligible and evaluable patients were accrued to stratum 3. In stratum 1, nine (36% [95% CI 18-57]) of 25 patients achieved a sustained partial response. The median follow-up for the 11 patients who had not had a progression event by Aug 9, 2018, was 36·40 months (IQR 21·72-45·59). In stratum 3, ten (40% [21-61]) of 25 patients achieved a sustained partial response; median follow-up was 48·60 months (IQR 39·14-51·31) for the 17 patients without a progression event by Aug 9, 2018. The most frequent grade 3 or worse adverse events were elevated creatine phosphokinase (five [10%]) and maculopapular rash (five [10%]). No treatment-realted deaths were reported.

interpretationSelumetinib is active in recurrent, refractory, or progressive pilocytic astrocytoma harbouring common BRAF aberrations and NF1-associated paediatric low-grade glioma. These results show that selumetinib could be an alternative to standard chemotherapy for these subgroups of patients, and have directly led to the development of two Children's Oncology Group phase 3 studies comparing standard chemotherapy to selumetinib in patients with newly diagnosed paediatric low-grade glioma both with and without NF1.

fundingNational Cancer Institute Cancer Therapy Evaluation Program, the American Lebanese Syrian Associated Charities, and AstraZeneca.

Indexed as

AdolescentBenzimidazolesCentral Nervous System NeoplasmsChildChild, PreschoolDisease ProgressionFemaleGliomaHumansMaleNeoplasm GradingNeoplasms, Multiple PrimaryNeurofibromatosis 1Proto-Oncogene Proteins B-rafYoung AdultAZD 6244BenzimidazolesBRAF protein, humanProto-Oncogene Proteins B-raf

Identifiers

PMID31151904
PMCPMC6628202
OpenAlexW2947767395

What OpenQuestion holds

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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 OpenQuestion graph.