Evidence map›Paper›PMID 39594714›Full record

ArticleCancers2024

Brain Metastases in Sarcomas: A Multicenter Retrospective Cohort Study.

Ellen Zhang, Sheima Farag, Hilary Dietz, Daniel Wang, Angela Hirbe, Kristen Ganjoo, Brian Van Tine, Shane Zaid, Aisha Miah, Vicki Keedy and 2 more

Abstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. 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

12 authors.

Ellen ZhangDepartment of Medicine Division of Oncology, Stanford University School of Medicine, Stanford, CA 94304, USA.ORCID 0000-0001-5365-4209
Sheima FaragRoyal Marsden Hospital, London SW3 6JJ, UK.
Hilary DietzCayuga Health, Ithaca, NY 14850, USA.
Daniel WangBaylor College of Medicine, Houston, TX 77030, USA.
Angela HirbeDivision of Oncology, Washington University in St. Louis, St. Louis, MO 63130, USA.ORCID 0000-0003-1719-0771
Kristen GanjooDepartment of Medicine Division of Oncology, Stanford University School of Medicine, Stanford, CA 94304, USA.
Brian Van TineDivision of Oncology, Washington University in St. Louis, St. Louis, MO 63130, USA.ORCID 0000-0003-4572-6668
Shane ZaidRoyal Marsden Hospital, London SW3 6JJ, UK.
Aisha MiahRoyal Marsden Hospital, London SW3 6JJ, UK.ORCID 0000-0001-6946-0820
Vicki KeedyDivision of Hematology/Oncology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Elizabeth DavisDivision of Hematology/Oncology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID 0000-0001-7626-2435
Nam BuiDepartment of Medicine Division of Oncology, Stanford University School of Medicine, Stanford, CA 94304, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeBrain metastases (BM) in sarcomas occur rarely and are associated with poor prognosis. This study is a large retrospective cohort describing the demographic and clinical characteristics of these patients, treatment strategies, and survival outcomes.

methodsIn total, 81 patients with BM from sarcomas were identified across five sarcoma centers. Demographic data, clinical presentation, and treatment modalities were analyzed.

resultsThe most common histologies were leiomyosarcoma (12.3%) and undifferentiated pleomorphic sarcoma (12.3%). The median time from sarcoma diagnosis to brain metastases was 1.9 years. Upon presentation, 88.9% of patients with BM from sarcomas were symptomatic with the most common presenting symptom being focal neurological deficits (37.9%) and headaches (22.1%). Higher-grade sarcomas were more likely to metastasize and were usually preceded by metastases to other sites, most commonly the lungs. One-year overall survival was 31% from initial sarcoma diagnosis, and the median time from diagnosis of BM until death was 6.0 months. For treatment, 60 (74.1%) patients had radiation, 39 (48.1%) patients had systemic therapy, and 29 (35.8%) patients had surgery. In a multivariate analysis, surgery (HR 0.30) and chemotherapy (HR 0.23) were found to be significantly correlated with improved survival outcomes. Although radiation as a whole was not found to significantly correlate with survival, improved outcomes were seen with stereotactic radiosurgery (SRS, mOS 11.6 mo) as opposed to whole-brain radiation therapy (WBRT, mOS 8.3 mo). Additionally, patients with leptomeningeal disease were significantly less likely to survive more than one year compared to patients with brain metastases only.

conclusionsOur findings identify that patients with metastatic sarcoma to the brain have poor prognoses, often have concurrent metastasis, and have a median survival of only 6 months. Additionally, our study found that leptomeningeal metastases is a rare presentation with poor survival outcomes. There are various treatment modalities for sarcomas with BM; however, there are no guidelines, unlike in other malignancies. Further research is necessary to evaluate the role of therapeutic measures in terms of type, timing, and outcomes.

Indexed as

brain metastaseschemotherapydisease prognosisincidencemortalityradiationsarcomasurgery

Identifiers

PMID39594714
PMCPMC11591821

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.