Evidence map›Paper›PMID 42776319›Full record

ArticleJournal of neuro-oncology2026

Supplementary motor area syndrome in intracranial gliomas is not associated with worse survival.

Dragan Jankovic, Sophie Rosenke, Jens Blobner, Andrea Szelényi, Veit Stöcklein, Santhosh G Thavarajasingam, Andreas Kramer, Philipp Karschnia, Nico Teske, Florian Ringel and 1 more

Abstract read
In one paragraph

Article in Journal of neuro-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.

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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

11 authors.

Dragan JankovicDepartment of Neurosurgery, LMU University Hospital, LMU Medizin, Ludwig- Maximilians-Universität, Munich, Germany.
Sophie RosenkeFaculty of Medicine, Lancaster University, Lancaster, UK.
Jens BlobnerDepartment of Neurosurgery, LMU University Hospital, LMU Medizin, Ludwig- Maximilians-Universität, Munich, Germany.
Andrea SzelényiDepartment of Neurosurgery, LMU University Hospital, LMU Medizin, Ludwig- Maximilians-Universität, Munich, Germany.
Veit StöckleinDepartment of Neurosurgery, LMU University Hospital, LMU Medizin, Ludwig- Maximilians-Universität, Munich, Germany.
Santhosh G ThavarajasingamDepartment of Neurosurgery, LMU University Hospital, LMU Medizin, Ludwig- Maximilians-Universität, Munich, Germany.
Andreas KramerDepartment of Neurosurgery, LMU University Hospital, LMU Medizin, Ludwig- Maximilians-Universität, Munich, Germany.
Philipp KarschniaDepartment of Neurosurgery, Technical University Munich, Munich, Germany.
Nico TeskeDepartment of Neurosurgery, Uniklinikum Erlangen, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany.
Florian RingelDepartment of Neurosurgery, LMU University Hospital, LMU Medizin, Ludwig- Maximilians-Universität, Munich, Germany.
Darius KalasauskasDepartment of Neurosurgery, LMU University Hospital, LMU Medizin, Ludwig- Maximilians-Universität, Munich, Germany. Darius.Kalasauskas@med.uni-muenchen.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeResection of gliomas involving the supplementary motor area (SMA) carries a substantial risk of postoperative functional deficits, which may affect patients' ability to undergo adjuvant therapy. This study evaluated whether postoperative SMA syndrome is associated with delayed initiation of adjuvant therapy and with progression-free survival (PFS) and overall survival (OS).

methodsWe performed a retrospective single-center study of patients undergoing resection of gliomas involving, adjacent to, or approached through the SMA between 2015 and 2024. SMA syndrome was defined as new-onset motor deficits and/or language impairment without corresponding intraoperative neuromonitoring changes and without involvement of the primary motor cortex or corticospinal tract. Logistic and Cox regression analyses were performed.

resultsSeventy-four patients were included, of whom 37 (50%) developed postoperative SMA syndrome. In univariate logistic regression, RANO class 2 A and class 2B resections were associated with higher odds of postoperative SMA syndrome compared with RANO class 1 resections (p = 0.048 and p = 0.035, respectively). In the pairwise multivariable model, grouped RANO class 2 resections remained associated with higher odds of postoperative SMA syndrome compared with class 1 resections (OR 5.05, 95% CI 1.24-20.57; p = 0.024). Postoperative SMA syndrome was not associated with delayed initiation of adjuvant therapy (HR 0.86, 95% CI 0.49-1.53; p = 0.617), PFS (HR 1.21, 95% CI 0.63-2.32; p = 0.573), or OS (HR 1.21, 95% CI 0.49-2.95; p = 0.681). Postoperative functional decline (≥ 20-point KPS decrease) was independently associated with receipt of modified or reduced-intensity adjuvant therapy (adjusted OR 13.91, 95% CI 2.21-87.64; p = 0.005), whereas SMA syndrome itself was not associated with treatment modification.

conclusionsPostoperative SMA syndrome was not associated with delayed adjuvant therapy or worse survival. Functional status, rather than SMA syndrome, influenced treatment intensity, supporting maximal safe resection in the SMA region.

Indexed as

Brain NeoplasmsGliomaMotor CortexNeurosurgical ProceduresPostoperative ComplicationsAdultFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisRetrospective StudiesSurvival RateExtent of resectionFunctional outcomeGliomaSMA syndromeSupplementary motor area

Identifiers

PMID42776319
PMCPMC13601069

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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.