Evidence map›Paper›PMID 39713041›Full record

ArticleNeuro-oncology advances

Phase II trial of blood-brain barrier permeable peptide-paclitaxel conjugate ANG1005 in patients with recurrent high-grade glioma.

Crismita Dmello, Andrew Brenner, David Piccioni, Patrick Y Wen, Jan Drappatz, Maciej Mrugala, Lionel D Lewis, David Schiff, Camilo E Fadul, Marc Chamberlain and 5 more

Registry-linked trialAbstract read
In one paragraph

Article in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01967810 (A Phase II, Open-Label, Multi-Center Study of ANG1005 in Patients With Recurrent High-Grade Glioma), which is not on this map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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.

NCT01967810 phase2completednot on this map

A Phase II, Open-Label, Multi-Center Study of ANG1005 in Patients With Recurrent High-Grade Glioma

TypeinterventionalSponsorAngiochem IncRan2013 to 2017Enrolled73ConditionsGlioma, Glioblastoma, Brain Tumor, RecurrentArmsANG1005, Bevacizumab
3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

  1. Review
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  9. Targeting Survivin: Now I Become Death, the Destroyer of Cells.International journal of molecular sciences · 2025
    Review
  10. Review
  11. COG133 peptide-conjugated lipid nanoparticles sensitize medulloblastoma to radiation therapy in mice.Journal of controlled release : official journal of the Controlled Release Society · 2025
    Article
  12. Article
  13. Review
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  16. Nanomedicine for Glioblastoma Therapy: Novel Insights and Future Perspectives.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    Review
  17. 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

15 authors.

Crismita DmelloNorthwestern Medicine Malnati Brain Tumor Institute of the Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Chicago, Illinois, USA.
Andrew BrennerCancer Therapy and Research Center, University of Texas Health Science Center, San Antonio, Texas, USA.
David PiccioniDepartment of Neurosciences, UC San Diego Moores Cancer Center, La Jolla, California, USA.
Patrick Y WenCenter For Neuro-Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
Jan DrappatzDepartment of Neurology, UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, USA.
Maciej MrugalaFred Hutchinson Cancer Center, University of Washington Medical Center Seattle, Washington, USA.
Lionel D LewisDepartment of Medicine, Dartmouth-Hitchcock Medical Center Lebanon, New Hampshire, USA.
David SchiffEmily Couric Clinical Cancer Center, University of Virginia, Charlottesville, Virginia, USA.ORCID https://orcid.org/0000-0003-1561-9220
Camilo E FadulDivision of Neuro-Oncology, Department of Neurology, University of Virginia, Charlottesville, Virginia, USA.
Marc ChamberlainLantern Pharma, Dallas, Texas, USA.
Santosh KesariDepartment of Translational Neurosciences, Pacific Neuroscience Institute and Saint John's Cancer Institute at Providence Saint John's Health Center, Santa Monica, California, USA.
Manmeet AhluwaliaDepartment of Medical Oncology, Miami Cancer Institute, Miami, Florida, USA.
Debora GhoshDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical Center, Boston, Massachusetts, USA.
Adam M SonabendNorthwestern Medicine Malnati Brain Tumor Institute of the Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Chicago, Illinois, USA.
Priya KumthekarDepartment of Neurology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0001-5923-0677

Funding

STINGing GBM: A First-in- Man Clinical Trial in Surgical Resectable Recurrent GBMP50CA221747 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Atique U. Ahmed · 2018 to 2026
$21.4M
Leveraging doxorubicin immune-modulation, blood-brain barrier opening, and personalized medicine for effective immunotherapy in glioblastoma. A mechanistic approach and pharmacokinetic trial.U19CA264338 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Nicholas A Butowski · 2021 to 2026
$5.8M
Blood-brain barrier disruption with implantable ultrasound to enhance paclitaxel delivery: A Phase 1-2 clinical trial in recurrent glioblastomaR01CA245969 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Adam M Sonabend, Roger Stupp · 2020 to 2026
$2.8M
MAPK as target of glioma immunoediting by CD8 T-cells, and predictor of response to immunotherapyR01NS110703 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SONABEND, ADAM M · 2020 to 2024
$1.9M
NCI NIH HHS P50 CA221747NCI NIH HHS R01 CA245969NCI NIH HHS U19 CA264338NINDS NIH HHS R01 NS110703
6 · The paper itself

Abstract

Background: This study is a phase II clinical trial to evaluate the efficacy, safety, and tolerability of the blood-brain barrier (BBB) permeable peptide-paclitaxel conjugate ANG1005 in patients with recurrent high-grade glioma (HGG) (NCT01967810). Methods: Seventy-three patients were enrolled in 3 separate arms-recurrent glioblastoma (GBM) (Arm 1), bevacizumab refractory GBM (Arm 2), and grade 3 anaplastic gliomas (AGs) (Arm 3). The study was started in October 2013, and the data were locked on September 29, 2017. Safety was evaluated for all three arms ( Results: Overall, the safety of ANG1005 was found to be consistent with a taxane toxicity profile. Otherwise, the primary efficacy endpoints of ORR and PFS were not met. The most common adverse events (AEs) were hematologic (32.9%), alopecia (31.5%), and fatigue (30.1%). The median PFS was 1.4 months (95% CI: 1.4, 2.1) and similar across all the treatment arms. The median overall survival was 13.4 months (95% CI: 3.4, 14.6) in Arm 1, 5.8 months (95% CI: 1.9, 9.7) in Arm 2, and 18.2 months (95% CI: 10.7, 35.3) in Arm 3. Conclusion: A dose of 600 mg/m

Indexed as

ANG1005high-grade gliomapaclitaxelphase II clinical trial

Identifiers

PMID39713041
PMCPMC11662161

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Registered trials

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.