Targeting Angiogenic Pathways and Combination Approaches

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Tumor Microenvironment".

Deadline for manuscript submissions: closed (29 February 2024) | Viewed by 1815

Special Issue Editors


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Guest Editor
1. Molecular Pharmacology Group, School of Pharmaceutical Sciences, Institute of Pharmaceutical Sciences of Western Switzerland, University of Geneva, 1211 Geneva, Switzerland
2. Institute of Pharmaceutical Sciences of Western Switzerland, University of Geneva, 1211 Geneva, Switzerland
3. Translational Research Center in Oncohaematology, 1211 Geneva, Switzerland
Interests: combination therapy; tumor microenvirontment; targeted therapy; angiogenesis
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Guest Editor
Angiogenesis Laboratory, Department of Medical Oncology, Amsterdam UMC, Cancer Center Amsterdam, 1081 HV Amsterdam, The Netherlands
Interests: angiogenesis; immunotherapy; vascular biology
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Targeting of the tumor vasculature is attracting renewed attention because of the observed benefit of this therapeutic strategy in combination therapies. A great example is the enhanced efficacy of immunotherapy in combination with angiogenesis inhibitors. This is best observed in, but not limited to, checkpoint inhibition therapy. Thus, the continued development of anti-angiogenic strategies, as well as identification of attractive targets in the tumor vasculature, is critical. Additionally, when these strategies are used alongside other cancer therapies, synergism with anti-angiogenic approaches is seen, such as in chemo- and radiation therapy, as well as in hyperthermia and photodynamic therapy. 

In recent years, it has been demonstrated that anti-angiogenic therapy is beneficial when administered in combination with other therapies. Many strategies targeting the tumor vasculature have been developed, though they have received less attention because of the limited efficacy of anti-angiogenic drugs in cancer patients. This emphasizes the importance of targeting the tumor vasculature.

We are pleased to announce a Special Issue for Cancers entitled ‘Targeting Angiogenic Pathways and Combination Approaches’. The aim of this Special Issue is to draw attention to vascular targeting approaches and increase knowledge on the combination of this strategy with other cancer therapies, such as immune-, chemo-, radio- and photodynamic therapies.

The Special Issue aims to publish a collection of original research articles and reviews. Potential topics may include (but are not limited to):

  • New strategies for targeting the tumor vasculature.
  • Combination strategies of anti-angiogenic therapy and other anti-cancer approaches.
  • Enhanced insight in the mechanisms of angiogenesis and anti-angiogenesis.
  • In vitro, preclinical and clinical approaches of anti-angiogenesis and combination therapies.

We look forward to receiving your contributions.

Prof. Dr. Patrycja Nowak-Sliwinska
Prof. Dr. Arjan Griffioen
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Cancers is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2900 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • vascular targeting
  • anti-angiogenic therapy
  • combination therapy
  • targeted therapy
  • immunotherapy

Published Papers (1 paper)

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Research

14 pages, 2519 KiB  
Article
Vaccination against Extracellular Vimentin for Treatment of Urothelial Cancer of the Bladder in Client-Owned Dogs
by Diederik J. M. Engbersen, Judy R. van Beijnum, Arno Roos, Marit van Beelen, Jan David de Haan, Guy C. M. Grinwis, Jack A. Schalken, J. Alfred Witjes, Arjan W. Griffioen and Elisabeth J. M. Huijbers
Cancers 2023, 15(15), 3958; https://doi.org/10.3390/cancers15153958 - 3 Aug 2023
Cited by 2 | Viewed by 1501
Abstract
It was recently shown that targeting extracellular vimentin (eVim) is safe and effective in preclinical models. Here, we report the safety and efficacy in client-owned dogs with spontaneous bladder cancer of CVx1, an iBoost technology-based vaccine targeting eVim in combination with COX-2 inhibition. [...] Read more.
It was recently shown that targeting extracellular vimentin (eVim) is safe and effective in preclinical models. Here, we report the safety and efficacy in client-owned dogs with spontaneous bladder cancer of CVx1, an iBoost technology-based vaccine targeting eVim in combination with COX-2 inhibition. This was a single-arm prospective phase 1/2 study with CVx1 in 20 client-owned dogs with spontaneous UC which involved four subcutaneous vaccinations with CVx1 at 2-week intervals for induction of antibody titers, followed by maintenance vaccinations at 2-month intervals. Additionally, daily cyclooxygenase (COX)-2 inhibition with meloxicam was given. The response was assessed by antibody titers, physical condition, abdominal ultrasound and thorax X-ray. The primary endpoints were the development of antibody titers, as well as overall survival compared to a historical control group receiving carboplatin and COX-2 inhibition with piroxicam. Kaplan–Meier survival analysis was performed. All dogs developed antibodies against eVim. Titers were adequately maintained for the duration of this study. A median overall survival of 374 days was observed, which was 196 days for the historical control group (p < 0.01). Short-term grade 1–2 toxicity at the injection site and some related systemic symptoms peri-vaccination were observed. No toxicity was observed related to the induced antibody response. A limitation of this study is the single-arm prospective setting. CVx1 plus meloxicam consistently induced efficient antibody titers, was well tolerated and showed prolonged survival. The results obtained merit further development for human clinical care. Full article
(This article belongs to the Special Issue Targeting Angiogenic Pathways and Combination Approaches)
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