Evidence map›Paper›PMID 41491335›Full record

SynthesisNeurosurgical review2026

Management of intracranial undifferentiated pleomorphic sarcoma: a systematic review.

Noah B Drewes, Jeffrey Z Nie, Rafal Chojak, Khizar R Nandoliya, Rishi Jain, Harrshavasan Congivaram, Umme H Faisal, Lara Koutah, Niyant Vora, Elek A Wellman and 8 more

Abstract readSystematic Review
In one paragraph

Synthesis in Neurosurgical review, 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
–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

18 authors.

Noah B DrewesDepartment of Surgery, Division of Neurosurgery, Southern Illinois University School of Medicine, Springfield, IL, USA. ndrewes45@siumed.edu.ORCID http://orcid.org/0009-0006-2636-0516
Jeffrey Z NieDepartment of Neurosurgery, Neurological Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.ORCID http://orcid.org/0000-0001-5213-4252
Rafal ChojakDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. rafal.chojak@northwestern.edu.ORCID http://orcid.org/0000-0002-7644-3444
Khizar R NandoliyaDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.ORCID http://orcid.org/0000-0002-6616-4388
Rishi JainDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.ORCID http://orcid.org/0000-0003-4459-5504
Harrshavasan CongivaramDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.ORCID http://orcid.org/0009-0003-5897-0560
Umme H FaisalDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.ORCID http://orcid.org/0000-0002-0486-2391
Lara KoutahDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.ORCID http://orcid.org/0000-0003-0991-0978
Niyant VoraDepartment of Surgery, Division of Neurosurgery, Southern Illinois University School of Medicine, Springfield, IL, USA.
Elek A WellmanDepartment of Surgery, Division of Neurosurgery, Southern Illinois University School of Medicine, Springfield, IL, USA.ORCID http://orcid.org/0000-0002-9755-3212
Matthew W WeberDepartment of Surgery, Division of Neurosurgery, Southern Illinois University School of Medicine, Springfield, IL, USA.ORCID http://orcid.org/0000-0002-3606-5346
Nathan J NordmannDepartment of Surgery, Division of Neurosurgery, Southern Illinois University School of Medicine, Springfield, IL, USA.ORCID http://orcid.org/0000-0002-7106-8665
Jeffrey W CozzensDepartment of Surgery, Division of Neurosurgery, Southern Illinois University School of Medicine, Springfield, IL, USA.ORCID http://orcid.org/0000-0003-4576-6942
Devin V AminDepartment of Surgery, Division of Neurosurgery, Southern Illinois University School of Medicine, Springfield, IL, USA.
Jose A EspinosaDepartment of Surgery, Division of Neurosurgery, Southern Illinois University School of Medicine, Springfield, IL, USA.
Breck JonesDepartment of Surgery, Division of Neurosurgery, Southern Illinois University School of Medicine, Springfield, IL, USA.
Bruce M FrankelDepartment of Surgery, Division of Neurosurgery, Southern Illinois University School of Medicine, Springfield, IL, USA.
Leslie Acakpo-SatchiviDepartment of Surgery, Division of Neurosurgery, Southern Illinois University School of Medicine, Springfield, IL, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Undifferentiated pleomorphic sarcoma (UPS) is a rare and aggressive soft tissue tumor of unknown histogenesis. UPS most often arises in the extremities or trunk, where wide surgical excision is feasible. Rarely, UPS involves the intracranial space, where critical structures may inhibit complete resection. Given its rarity and historical misclassification as malignant fibrous histiocytoma (MFH), knowledge of intracranial UPS is limited, and there are no clear treatment guidelines. We systematically reviewed all available cases of intracranial UPS to consolidate existing literature and assess prognosis and management considerations. A systematic review was conducted according to PRISMA guidelines. PubMed and Embase were searched for reports of intracranial UPS or storiform-pleomorphic MFH. Eligible studies included at least one histologically confirmed case treated with surgery, chemotherapy, or radiotherapy and reported outcomes. Data on demographics, tumor location, treatment, follow-up, and survival were extracted. Event-free survival (EFS) and overall survival (OS) were analyzed by treatment modality, age, sex, and tumor location using Kaplan-Meier and log-rank tests. From 801 records, 40 studies with 48 patients were included. The median age was 45 years, and 50% were female. 15% had prior radiotherapy. Most tumors were extra-axial (45%) and nearly all patients underwent surgery, with 82.1% achieving gross total resection. Median EFS and OS were 18 and 24 months, respectively. No survival differences were seen by treatment modality, age, or sex. Overall survival was longer for extra-axial tumors compared to intra-axial or skull base tumors (p = 0.016). Intracranial UPS is a rare and aggressive tumor, with worse prognosis compared to those that are extracranial. Among factors that we evaluated, extra-axial location was the strongest positive prognostic factor. Surgical resection with adjuvant chemoradiation showed the longest median survival. Ongoing case reports are required to refine management guidelines and improve patient outcomes.

Indexed as

Brain NeoplasmsHistiocytoma, Malignant FibrousSarcomaFemaleHumansMaleMiddle AgedNeurosurgical ProceduresBrain tumorsMalignant fibrous histiocytomaNeurosurgeryPrognosisSystematic reviewUndifferentiated pleomorphic sarcoma

Identifiers

PMID41491335
PMCPMC12769503

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Registered trials

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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.