Evidence map›Paper›PMID 42168485›Full record

ArticleNPJ precision oncology2026

Machine learning in automatic detection of chordoma signature, postoperative residuals, and prognosis of skull base chordomas.

Daniela Stastna, Richard Mannion, Robert Macfarlane, Patrick Axon, Neil Donnelly, James R Tysome, Daniele Borsetto, Ryan Chrenek, Kaasinath Balagurunath, Wenya Linda Bi and 5 more

Abstract read
In one paragraph

Article in NPJ precision oncology, 2026. 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
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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

15 authors.

Daniela StastnaSkull Base Unit, Cambridge University Hospitals, Cambridge, UK. dany.stastna@gmail.com.
Richard MannionSkull Base Unit, Cambridge University Hospitals, Cambridge, UK.
Robert MacfarlaneSkull Base Unit, Cambridge University Hospitals, Cambridge, UK.
Patrick AxonSkull Base Unit, Cambridge University Hospitals, Cambridge, UK.
Neil DonnellySkull Base Unit, Cambridge University Hospitals, Cambridge, UK.
James R TysomeSkull Base Unit, Cambridge University Hospitals, Cambridge, UK.
Daniele BorsettoSkull Base Unit, Cambridge University Hospitals, Cambridge, UK.
Ryan ChrenekSkull Base unit, Mass General Brigham Hospital, Harvard University, Boston, MA, USA.
Kaasinath BalagurunathSkull Base unit, Mass General Brigham Hospital, Harvard University, Boston, MA, USA.
Wenya Linda BiSkull Base unit, Mass General Brigham Hospital, Harvard University, Boston, MA, USA.
Carleton E CorralesSkull Base unit, Mass General Brigham Hospital, Harvard University, Boston, MA, USA.
Ossama Al-MeftySkull Base unit, Mass General Brigham Hospital, Harvard University, Boston, MA, USA.
Timothy SmithSkull Base unit, Mass General Brigham Hospital, Harvard University, Boston, MA, USA.
Ari ErcolePerioperative, Acute, Critical Care and Emergency Medicine (PACE), Department of Medicine, Cambridge University Hospitals, Cambridge, UK.
Jonathan ColesPerioperative, Acute, Critical Care and Emergency Medicine (PACE), Department of Medicine, Cambridge University Hospitals, Cambridge, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Skull base chordomas are rare, locally invasive tumors that remain a diagnostic and therapeutic challenge. We developed a machine-learning (ML) radiomics model to (i) distinguish chordoma from chondrosarcoma and skull base background, (ii) differentiate true postoperative residual tumor from treatment-related changes, and (iii) predict 2-year progression-free survival (PFS). In this retrospective, dual-center study, 61 patients underwent surgery between 1998 and 2023. Preoperative contrast-enhanced T1-weighted MRI images were pre-processed and segmented; data were augmented by 20%. ML models included nested cross-validated XGBoost and a 4-layer standard feedforward Multilayer Perceptron (MLP) (Python, Keras). The primary and secondary endpoints were diagnostic discrimination and residual-versus-treatment-related change classification; the exploratory endpoint was 2-year PFS prediction. XGBoost achieved diagnostic accuracy of 0.90 (95% CI: 0.84-0.96) in distinguishing chordoma from chondrosarcoma/skull base background, and residual-versus-change accuracy 0.91 (95% CI: 0.85-0.96). PFS prediction reached an accuracy of 0.87 (95% CI: 0.74-0.98). MLP showed comparable performance (diagnostic validation accuracy 0.89; residual classification 0.90; PFS 0.93). To our knowledge, this is the first dual-center MRI-based ML study to jointly address preoperative histologic discrimination, postoperative residual detection, and short-term PFS prediction in a small, heterogeneous cohort. These results support future clinical translation as a noninvasive decision-support tool for preoperative assessment, postoperative surveillance, and risk stratification.

Identifiers

PMID42168485
PMCPMC13661533

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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.