Evidence map›Paper›PMID 35344029›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2022

Infigratinib in Patients with Recurrent Gliomas and FGFR Alterations: A Multicenter Phase II Study.

Andrew B Lassman, Juan Manuel Sepúlveda-Sánchez, Timothy F Cloughesy, Miguel J Gil-Gil, Vinay K Puduvalli, Jeffrey J Raizer, Filip Y F De Vos, Patrick Y Wen, Nicholas A Butowski, Paul M J Clement and 10 more

Open access · hybridAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
13.3field-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.

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

78 citing papers in PubMed, 91 citations in OpenAlex.

  1. Trial
  2. Next-generation therapeutics for glioblastoma: Challenges and future directions.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Review
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  9. Recent Advances in Targeted Therapies for Adult Gliomas.Current neurology and neuroscience reports · 2026
    Review
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  13. Article
  14. Review
  15. Sprouty in Tumors of the Nervous System.International journal of molecular sciences · 2025
    Review
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  20. Review

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

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

20 authors at 14 institutions in 5 countries.

Andrew B LassmanDivision of Neuro-Oncology, Department of Neurology and Herbert Irving Comprehensive Cancer Center, Columbia University Vagelos College of Physicians and Surgeons and NewYork-Presbyterian, New York, New York.ORCID 0000-0001-7386-9928
Juan Manuel Sepúlveda-SánchezHospital Universitario 12 De Octubre, Madrid, Spain.
Timothy F CloughesyUniversity of California at Los Angeles, Los Angeles, California.
Miguel J Gil-GilInstitut Català d'Oncologia, Hospitalet de Llobregat, Barcelona, Spain.ORCID 0000-0003-1380-2718
Vinay K PuduvalliDivision of Neuro-Oncology, Ohio State University Wexner Medical Center, Columbus, Ohio.
Jeffrey J RaizerNorthwestern University, Department of Neurology, Section of Neuro-Oncology, Chicago, Illinois.
Filip Y F De VosDepartment Medical Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID 0000-0002-9082-5991
Patrick Y WenCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Nicholas A ButowskiUniversity of California San Francisco, San Francisco, California.ORCID 0000-0001-5162-2406
Paul M J ClementLeuven Cancer Institute, KU Leuven, Leuven, Belgium.ORCID 0000-0001-7600-0806
Morris D GrovesTexas Oncology PA, Austin, Texas.
Cristóbal Belda-IniestaHospital Universitario HM Sanchinarro, Madrid, Spain.
Pierre GiglioDivision of Neuro-Oncology, Ohio State University Wexner Medical Center, Columbus, Ohio.
Harris S SoiferQED Therapeutics, San Francisco, California.
Steven RowseyQED Therapeutics, San Francisco, California.
Cindy XuQED Therapeutics, San Francisco, California.
Francesca AvogadriQED Therapeutics, San Francisco, California.
Ge WeiQED Therapeutics, San Francisco, California.
Susan MoranQED Therapeutics, San Francisco, California.
Patrick RothDepartment of Neurology & Brain Tumor Center, University Hospital and University of Zurich, Zurich, Switzerland.
Rapt Therapeutics (United States) · USThe Ohio State University Wexner Medical Center · USCenter for Neuro-Oncology · USColumbia University · USHospital Universitario 12 De Octubre · ESHospital Universitario HM Sanchinarro · ESInstitut Català d'Oncologia · ESMidwestern University · USTexas Oncology · USUniversity Hospital of Zurich · CHUniversity of California, Los Angeles · USUniversity of California, San Francisco · USUtrecht University · NLVIB-KU Leuven Center for Cancer Biology · BE

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
UCLA SPORE in Brain CancerP50CA211015 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Yvonne Yu-Hsuan Chen · 2017 to 2026
$25.2M
Columbia University NCI Community Oncology Research ProgramUG1CA189960 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Jennifer E. Amengual, Lisa A. Kachnic · 2014 to 2026
$12.7M
NCI NIH HHS P30 CA013696NCI NIH HHS P50 CA211015NCI NIH HHS UG1 CA189960
6 · The paper itself

Abstract

purposeFGFR genomic alterations (amplification, mutations, and/or fusions) occur in ∼8% of gliomas, particularly FGFR1 and FGFR3. We conducted a multicenter open-label, single-arm, phase II study of a selective FGFR1-3 inhibitor, infigratinib (BGJ398), in patients with FGFR-altered recurrent gliomas. PATIENTS AND

methodsAdults with recurrent/progressive gliomas harboring FGFR alterations received oral infigratinib 125 mg on days 1 to 21 of 28-day cycles. The primary endpoint was investigator-assessed 6-month progression-free survival (PFS) rate by Response Assessment in Neuro-Oncology criteria. Comprehensive genomic profiling was performed on available pretreatment archival tissue to explore additional molecular correlations with efficacy.

resultsAmong 26 patients, the 6-month PFS rate was 16.0% [95% confidence interval (CI), 5.0-32.5], median PFS was 1.7 months (95% CI, 1.1-2.8), and objective response rate was 3.8%. However, 4 patients had durable disease control lasting longer than 1 year. Among these, 3 had tumors harboring activating point mutations at analogous positions of FGFR1 (K656E; n = 2) or FGFR3 (K650E; n = 1) in pretreatment tissue; an FGFR3-TACC3 fusion was detected in the other. Hyperphosphatemia was the most frequently reported treatment-related adverse event (all-grade, 76.9%; grade 3, 3.8%) and is a known on-target toxicity of FGFR inhibitors.

conclusionsFGFR inhibitor monotherapy with infigratinib had limited efficacy in a population of patients with recurrent gliomas and different FGFR genetic alterations, but durable disease control lasting more than 1 year was observed in patients with tumors harboring FGFR1 or FGFR3 point mutations or FGFR3-TACC3 fusions. A follow-up study with refined biomarker inclusion criteria and centralized FGFR testing is warranted.

Indexed as

GliomaNeoplasm Recurrence, LocalAdultFollow-Up StudiesHumansMicrotubule-Associated ProteinsPhenylurea CompoundsProtein Kinase InhibitorsPyrimidinesReceptor, Fibroblast Growth Factor, Type 3infigratinibMicrotubule-Associated ProteinsPhenylurea CompoundsProtein Kinase InhibitorsPyrimidinesReceptor, Fibroblast Growth Factor, Type 3TACC3 protein, human

Identifiers

PMID35344029
PMCPMC9167702
OpenAlexW4220760248

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.