Evidence map›Paper›PMID 39900703›Full record

ArticlePituitary2025

The role of BRAF testing of Rathke's cleft cysts to identify missed papillary craniopharyngioma.

Nicholas G Candy, E Mignone, E Quick, B Koszyca, A Brown, I M Chapman, D J Torpy, N Vrodos, S Santoreneos, S M C De Sousa

Abstract read
In one paragraph

Article in Pituitary, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. The endocrine spectrum of Rathke cleft cysts.Frontiers in endocrinology · 2025
    Review
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

10 authors.

Nicholas G CandyDepartment of Surgery - Otolaryngology, Head and Neck Surgery, The University of Adelaide, Basil Hetzel Institute for Translational Research, Woodville South, Adelaide, Australia. nicholas.candy@adelaide.edu.au.
E MignoneEndocrine and Metabolic Unit, Royal Adelaide Hospital, Adelaide, Australia.
E QuickSA Pathology, Flinders Medical Centre, Adelaide, Australia.
B KoszycaSA Pathology, Royal Adelaide Hospital, Adelaide, Australia.
A BrownDepartment of Genetics and Molecular Pathology, SA Pathology, Adelaide, SA, Australia.
I M ChapmanEndocrine and Metabolic Unit, Royal Adelaide Hospital, Adelaide, Australia.
D J TorpyEndocrine and Metabolic Unit, Royal Adelaide Hospital, Adelaide, Australia.
N VrodosDepartment of Neurosurgery, Flinders Medical Centre, Adelaide, Australia.
S SantoreneosDepartment of Neurosurgery, Royal Adelaide Hospital, Adelaide, Australia.
S M C De SousaEndocrine and Metabolic Unit, Royal Adelaide Hospital, Adelaide, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThe differential diagnosis of cystic sellar/suprasellar lesions includes craniopharyngioma (CP) and Rathke's cleft cyst (RCC). Histological differentiation between cystic papillary craniopharyngioma (pCP) and RCC using light microscopy alone is challenging. A major point of difference is that virtually all pCPs are clonal for the BRAF V600E variant, whereas RCCs are not. Noting that BRAF testing of RCCs is not current standard practice, we hypothesised that routinely performing BRAF studies in RCCs might uncover otherwise missed pCPs.

methodWe performed a retrospective cohort study of all RCCs operated on at Flinders Medical Centre, the Memorial and Royal Adelaide Hospitals, between 2001 and 2023. In cases with sufficient tissue, we performed BRAF V600E immunohistochemistry (IHC) and BRAF next generation sequencing (NGS) of extracted tumour DNA.

resultsOf eleven patients with suitable operative specimens, one patient with an initial diagnosis of RCC was revised to pCP following BRAF testing with equivocal positivity on BRAF IHC and clear identification of the V600E variant on NGS. The patient's subsequent clinical course was aggressive and more compatible with pCP than RCC.

conclusionThis study highlights the potential value of BRAF testing in RCCs to identify missed pCP, which is an especially timely finding given the advent of primary medical therapy with BRAF inhibition for pCP. In the absence of guidelines advising on the use of BRAF studies in sellar lesions, we suggest consideration of BRAF testing of all RCCs, particularly if there is squamous metaplasia or disease recurrence.

Indexed as

Central Nervous System CystsCraniopharyngiomaPituitary NeoplasmsProto-Oncogene Proteins B-rafAdolescentAdultAgedFemaleHigh-Throughput Nucleotide SequencingHumansImmunohistochemistryMaleMiddle AgedRetrospective StudiesYoung AdultBRAF protein, humanProto-Oncogene Proteins B-rafBRAFCraniopharyngiomaEndoscopic endonasal surgeryPapillary craniopharyngiomaRathke’s cleft cyst

Identifiers

PMID39900703
PMCPMC11790742

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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.