Evidence map›Paper›PMID 34623599›Full record

SynthesisJournal of neuro-oncology2021

Leptomeningeal disease in glioblastoma: endgame or opportunity?

Sarfraz Akmal, Elizabeth E Ginalis, Nitesh V Patel, Robert Aiken, Alis J Dicpinigaitis, Simon J Hanft

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Journal of neuro-oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% of its field
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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Obstacles and Trials in Treating Primary Brain Tumors.International journal of molecular sciences · 2026
    Review
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  5. Article
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  17. Safety and Efficacy of Intraventricular Immunovirotherapy with Oncolytic HSV-1 for CNS Cancers.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
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  19. 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

6 authors at 3 institutions in 1 country.

Sarfraz AkmalDepartment of Neurosurgery, Rutgers-Robert Wood Johnson Medical School, New Brunswick, NJ, USA.
Elizabeth E GinalisDepartment of Neurosurgery, Rutgers-Robert Wood Johnson Medical School, New Brunswick, NJ, USA.
Nitesh V PatelDepartment of Neurosurgery, Rutgers-Robert Wood Johnson Medical School, New Brunswick, NJ, USA.
Robert AikenGerald J. Glasser Brain Tumor Center, Atlantic Health System, Summit, NJ, USA.
Alis J DicpinigaitisDepartment of Neurosurgery, Westchester Medical Center, New York Medical College, Valhalla, NY, USA.
Simon J HanftDepartment of Neurosurgery, Westchester Medical Center, New York Medical College, Valhalla, NY, USA. simon.hanft@wmchealth.org.ORCID http://orcid.org/0000-0002-9280-8319
Rutgers, The State University of New Jersey · USWestchester Medical Center · USAtlantic Health System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGlioblastoma is an aggressive cancer with a notoriously poor prognosis. Recent advances in treatment have increased overall survival, though this may be accompanied by an increased incidence of leptomeningeal disease (LMD). LMD carries a particularly severe prognosis and remains a late stage manifestation of glioblastoma without satisfactory treatment. The objective of this review is to survey the literature on treatment of LMD in glioblastoma and to more fully characterize the current therapeutic strategies.

methodsThe authors performed a systematic review following PRISMA criteria on PubMed and OVID databases. Articles that included adult patients with LMD from glioblastoma were retrieved and reviewed.

resultsLMD in glioblastoma patients is increasing in incidence, with reports of up to 21%. The overall survival without treatment is alarmingly brief, with patients surviving between 1.6-3.8 months. All studies showed that treatment does improve overall survival significantly, increasing to 11.7 months in one study. However, no one adjuvant or surgical therapy has been shown to improve survival in LMD significantly over another. Direct treatment methods include chemotherapy (standard, anti-angiogenic, intrathecal, immunotherapy), and radiation. Hydrocephalus is a complication in LMD that can be treated with ventriculoperitoneal shunt placement, however treating hydrocephalus and delivering intrathecal chemotherapy is a challenge.

conclusionThough evidence remains lacking and there is no consensus, treatments show a trend towards improving survival and should be considered on a case-by-case basis. Further studies are necessary in the pursuit of a standard of care.

Indexed as

GlioblastomaMeningeal NeoplasmsHumansPrognosisGlioblastomaLeptomeningeal diseaseLeptomeningeal metastasisNeuro-oncology

Identifiers

PMID34623599
OpenAlexW3195223672

What OpenQuestion holds

Textmetadata
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.