Evidence map›Paper›PMID 38578405›Full record

ReviewCurrent neurology and neuroscience reports2024

Strategies to Improve Drug Delivery Across the Blood-Brain Barrier for Glioblastoma.

Kazim H Narsinh, Edgar Perez, Alexander F Haddad, Jacob S Young, Luis Savastano, Javier E Villanueva-Meyer, Ethan Winkler, John de Groot

Open access · hybridAbstract readReview
In one paragraph

Review in Current neurology and neuroscience reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
34.6field-weighted citation impact, top 1% 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

73 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. CD97/Cells · 2026
    Review
  6. Article
  7. Article
  8. Chromosomal Instability Drives Glioblastoma Heterogeneity and Therapeutic Opportunities.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  9. Article
  10. Review
  11. Article
  12. FungalInternational journal of molecular sciences · 2026
    Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. Review

13 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Kazim H NarsinhDepartment of Neurologic Surgery, University of California, San Francisco, CA, USA. kazim.narsinh@ucsf.edu.
Edgar PerezDepartment of Neurologic Surgery, University of California, San Francisco, CA, USA.
Alexander F HaddadDepartment of Neurologic Surgery, University of California, San Francisco, CA, USA.
Jacob S YoungDepartment of Neurologic Surgery, University of California, San Francisco, CA, USA.
Luis SavastanoDepartment of Neurologic Surgery, University of California, San Francisco, CA, USA.
Javier E Villanueva-MeyerDepartment of Neurologic Surgery, University of California, San Francisco, CA, USA.
Ethan WinklerDepartment of Neurologic Surgery, University of California, San Francisco, CA, USA.
John de GrootDepartment of Neurologic Surgery, University of California, San Francisco, CA, USA.
University of California, San Francisco · US

Funding

Training Program in Translational Brain Tumor ResearchT32CA151022 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Joseph F Costello · 2010 to 2026
$6.6M
NCI NIH HHS T32 CA151022
6 · The paper itself

Abstract

purpose of reviewGlioblastoma remains resistant to most conventional treatments. Despite scientific advances in the past three decades, there has been a dearth of effective new treatments. New approaches to drug delivery and clinical trial design are needed. RECENT

findingsWe discuss how the blood-brain barrier and tumor microenvironment pose challenges for development of effective therapies for glioblastoma. Next, we discuss treatments in development that aim to overcome these barriers, including novel drug designs such as nanoparticles and antibody-drug conjugates, novel methods of drug delivery, including convection-enhanced and intra-arterial delivery, and novel methods to enhance drug penetration, such as blood-brain barrier disruption by focused ultrasound and laser interstitial thermal therapy. Lastly, we address future opportunities, positing combination therapy as the best strategy for effective treatment, neoadjuvant and window-of-opportunity approaches to simultaneously enhance therapeutic effectiveness with interrogation of on-treatment biologic endpoints, and adaptive platform and basket trials as imperative for future trial design. New approaches to GBM treatment should account for the blood-brain barrier and immunosuppression by improving drug delivery, combining treatments, and integrating novel clinical trial designs.

Indexed as

Antineoplastic AgentsBrain NeoplasmsGlioblastomaBlood-Brain BarrierDrug Delivery SystemsHumansTumor MicroenvironmentAntineoplastic AgentsClinical trialsConvection-enhanced deliveryDrug deliveryFocused ultrasoundGBMGlioblastomaLaser interstitial thermal therapy

Identifiers

PMID38578405
PMCPMC11016125
OpenAlexW4393987766

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.