Evidence map›Paper›PMID 37631236›Full record

ReviewPharmaceutics2023

Induced Vascular Normalization-Can One Force Tumors to Surrender to a Better Microenvironment?

Xu Xin Sun, Zeynab Nosrati, Janell Ko, Che-Min Lee, Kevin L Bennewith, Marcel B Bally

Abstract readReview
In one paragraph

Review in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Trojan Horse Strategy: How Biomimetic Nanomedicine Remodels the Tumor Microenvironment.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  3. Article
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.

Xu Xin SunExperimental Therapeutics, BC Cancer Research Institute, Vancouver, BC V5Z 1L3, Canada.
Zeynab NosratiExperimental Therapeutics, BC Cancer Research Institute, Vancouver, BC V5Z 1L3, Canada.
Janell KoExperimental Therapeutics, BC Cancer Research Institute, Vancouver, BC V5Z 1L3, Canada.
Che-Min LeeExperimental Therapeutics, BC Cancer Research Institute, Vancouver, BC V5Z 1L3, Canada.
Kevin L BennewithExperimental Therapeutics, BC Cancer Research Institute, Vancouver, BC V5Z 1L3, Canada.
Marcel B BallyExperimental Therapeutics, BC Cancer Research Institute, Vancouver, BC V5Z 1L3, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy has changed the way many cancers are being treated. Researchers in the field of immunotherapy and tumor immunology are investigating similar questions: How can the positive benefits achieved with immunotherapies be enhanced? Can this be achieved through combinations with other agents and if so, which ones? In our view, there is an urgent need to improve immunotherapy to make further gains in the overall survival for those patients that should benefit from immunotherapy. While numerous different approaches are being considered, our team believes that drug delivery methods along with appropriately selected small-molecule drugs and drug candidates could help reach the goal of doubling the overall survival rate that is seen in some patients that are given immunotherapeutics. This review article is prepared to address how immunotherapies should be combined with a second treatment using an approach that could realize therapeutic gains 10 years from now. For context, an overview of immunotherapy and cancer angiogenesis is provided. The major targets in angiogenesis that have modulatory effects on the tumor microenvironment and immune cells are highlighted. A combination approach that, for us, has the greatest potential for success involves treatments that will normalize the tumor's blood vessel structure and alter the immune microenvironment to support the action of immunotherapeutics. So, this is reviewed as well. Our focus is to provide an insight into some strategies that will engender vascular normalization that may be better than previously described approaches. The potential for drug delivery systems to promote tumor blood vessel normalization is considered.

Indexed as

anti-angiogenesiscancer angiogenesisdrug repurposingimmune cellsimmune checkpoint inhibitorsimmunotherapynanomedicinetumor vascular normalization

Identifiers

PMID37631236
PMCPMC10458586

What OpenQuestion holds

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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.