Evidence map›Paper›PMID 39022647›Full record

ReviewNeuro-oncology advances

From bench to bedside: Advancing towards therapeutic treatment of vestibular schwannomas.

Shaolei Guo, Xuan Zheng, Wenli Chen, Umar Raza, Ailiang Zeng, Farhana Akter, Quan Huang, Shun Yao

Abstract readReview
In one paragraph

Review in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

8 authors.

Shaolei GuoDepartment of Neurosurgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xuan ZhengDepartment of Neurosurgery, The Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Wenli ChenDepartment of Neurosurgery, The Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Umar RazaSchool of Basic Medical Sciences, Shenzhen University, Shenzhen, China.
Ailiang ZengDepartment of Cancer Biology, UT MD Anderson Cancer Center, Houston, Texas, USA.
Farhana AkterFaculty of Arts and Sciences, Harvard University, Cambridge, Massachusetts, USA.
Quan HuangDepartment of Neurosurgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Shun YaoDepartment of Neurosurgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.ORCID https://orcid.org/0000-0003-1727-4078

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vestibular schwannomas are rare intracranial tumors originating from Schwann cells of the vestibular nerve. Despite their benign nature, these tumors can exert significant mass effects and debilitating symptoms, including gradual hearing loss, vertigo, facial nerve dysfunction, and headaches. Current clinical management options encompass wait-and-scan, surgery, radiation therapy, and off-label medication. However, each approach exhibits its own challenges and harbors limitations that underscore the urgent need for therapeutic treatments. Over the past 2 decades, extensive elucidation of the molecular underpinnings of vestibular schwannomas has unraveled genetic anomalies, dysregulated signaling pathways, downstream of receptor tyrosine kinases, disrupted extracellular matrix, inflammatory tumor microenvironment, and altered cerebrospinal fluid composition as integral factors in driving the development and progression of the disease. Armed with this knowledge, novel therapeutic interventions tailored to the unique molecular characteristics of those conditions are actively being pursued. This review underscores the urgency of addressing the dearth of Food and Drug Administration-approved drugs for vestibular schwannoma, highlighting the key molecular discoveries and their potential translation into therapeutics. It provides an in-depth exploration of the evolving landscape of therapeutic development, which is currently advancing from bench to bedside. These ongoing efforts hold the promise of significantly transforming the lives of vestibular schwannoma patients in the future.

Indexed as

angiogenesisinflammationreceptor tyrosine kinases (RTKs)targeted therapyvestibular schwannoma

Identifiers

PMID39022647
PMCPMC11252569

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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.