Evidence map›Paper›PMID 38815166›Full record

ArticleThe oncologist2025

Prolonged complete response to adjuvant tepotinib in a patient with newly diagnosed disseminated glioblastoma harboring mesenchymal-epithelial transition fusion.

Lily C Pham, Lauryn Weller, Claudia N Gann, Karl Maria Schumacher, Soetkin Vlassak, Todd Swanson, Kaitlin Highsmith, Barbara J O'Brien, Sebnem Nash, Ashley Aaroe and 2 more

Abstract readCase Reports
In one paragraph

Article in The oncologist, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–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

6 citing papers in PubMed.

  1. Vebreltinib for Previously Treated Astrocytoma,Cancer communications (London, England) · 2026
    Trial
  2. Article
  3. Review
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  5. Review
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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

12 authors.

Lily C PhamDepartment of Neurology, University of Maryland, Baltimore, MD, United States.
Lauryn WellerDepartment of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.ORCID 0009-0003-4392-0990
Claudia N GannBioNTech SE, Mainz, Germany.
Karl Maria SchumacherMerck Healthcare kGaA, Darmstadt, Germany.
Soetkin VlassakMerck Healthcare kGaA, Overijse, Belgium.
Todd SwansonDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Kaitlin HighsmithDepartment of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Barbara J O'BrienDepartment of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Sebnem NashDepartment of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Ashley AaroeDepartment of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
John F de GrootDepartment of Neuro-Oncology, University of California San Francisco, San Francisco, CA, United States.
Nazanin K MajdDepartment of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.ORCID 0000-0001-6451-544X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognosis of patients with glioblastoma (GBM) remains poor despite current treatments. Targeted therapy in GBM has been the subject of intense investigation but has not been successful in clinical trials. The reasons for the failure of targeted therapy in GBM are multifold and include a lack of patient selection in trials, the failure to identify driver mutations, and poor blood-brain barrier penetration of investigational drugs. Here, we describe a case of a durable complete response in a newly diagnosed patient with GBM with leptomeningeal dissemination and PTPRZ1-MET fusion who was treated with tepotinib, a brain-penetrant MET inhibitor. This case of successful targeted therapy in a patient with GBM demonstrates that early molecular testing, identification of driver molecular alterations, and treatment with brain-penetrant small molecule inhibitors have the potential to change the outcome in select patients with GBM.

Indexed as

Brain NeoplasmsGlioblastomaPiperidinesPyridazinesPyrimidinesHumansProto-Oncogene Proteins c-metPiperidinesProto-Oncogene Proteins c-metPyridazinesPyrimidinestepotinibglioblastomamolecular alterationoutcomestargeted therapytepotinib

Identifiers

PMID38815166
PMCPMC11783278

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.