Evidence map›Paper›PMID 40894434›Full record

ArticleJournal of neurological surgery. Part B, Skull base2025

Effect of Extent of Resection and Adjuvant Radiation on Recurrence of BRAF versus β-Catenin-Mutated Craniopharyngioma: A Single Institutional Case Series.

Maikerly Reyes, Patrick Kelly, KiChang Kang, Justin Williams, Anish Sathe, Allison Kayne, India Shelley, Giyarpuram Prashant, David Bray, Mark T Curtis and 1 more

Abstract read
In one paragraph

Article in Journal of neurological surgery. Part B, Skull base, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Maikerly ReyesSidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, Pennsylvania, United States.ORCID 0000-0002-3839-3001
Patrick KellyDepartment of Neurological Surgery at Thomas Jefferson University Hospital, Philadelphia, Pennsylvania, United States.
KiChang KangSidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, Pennsylvania, United States.ORCID 0000-0001-5203-1659
Justin WilliamsSidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, Pennsylvania, United States.
Anish SatheSidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, Pennsylvania, United States.
Allison KayneSidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, Pennsylvania, United States.
India ShelleySidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, Pennsylvania, United States.
Giyarpuram PrashantDepartment of Neurological Surgery at Thomas Jefferson University Hospital, Philadelphia, Pennsylvania, United States.
David BrayDepartment of Neurological Surgery at Thomas Jefferson University Hospital, Philadelphia, Pennsylvania, United States.
Mark T CurtisDepartment of Pathology, Anatomy, and Cell Biology at Thomas Jefferson University Hospital, Philadelphia, Pennsylvania, United States.
James J EvansDepartment of Neurological Surgery at Thomas Jefferson University Hospital, Philadelphia, Pennsylvania, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: The two histologic subtypes of craniopharyngiomas (CPs), papillary and adamantinomatous, harbor mutually exclusive mutations of BRAF V600E and CTNNB1, respectively. Studies suggest that subtotal resection (STR) plus adjuvant radiation therapy (XRT) may result in similar progression-free survival (PFS) as gross total resection (GTR). We hypothesized that STR ± XRT and GTR result in similar PFS for both BRAF and β-catenin-mutated CPs. Design: Patients who were surgically treated for a primary CP between 2001 and 2023 at a single institution were included. Immunohistochemical studies were performed retrospectively using BRAF and β-catenin antibodies. Patients with missing immunohistochemistry (IHC) diagnosis were excluded. Differences in PFS for STR ± XRT and GTR groups were assessed with a log-rank test, stratified by BRAF and β-catenin IHC status. Results: A total of 77 patients with CP were screened. IHC data were available for 50 patients; 20 had a BRAF mutation, and 30 had a β-catenin mutation. Among BRAF patients, 11 underwent GTR; 9 had STR, and 5 had adjuvant XRT. Among β-catenin patients, 14 underwent GTR; 16 had STR, and 6 had adjuvant XRT. For BRAF patients with GTR, the median PFS was not reached; for BRAF patients with STR ± XRT, the median PFS was 150 days ( Conclusions: Both GTR and STR ± XRT seemed to offer similar PFS outcomes only for patients with β-catenin-mutated CP. For patients with BRAF-mutated CP, a greater extent of resection was significantly associated with prolonged PFS.

Indexed as

BRAFcraniopharyngiomaβ-catenin

Identifiers

PMID40894434
PMCPMC12396883

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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.