Evidence map›Paper›PMID 32455560›Full record

ReviewCancers2020

Adenovirus and Immunotherapy: Advancing Cancer Treatment by Combination.

Mizuho Sato-Dahlman, Christopher J LaRocca, Chikako Yanagiba, Masato Yamamoto

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 48 citations in OpenAlex.

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  19. Construction and application of adenoviral vectors.Molecular therapy. Nucleic acids · 2023
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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

4 authors at 1 institution in 1 country.

Mizuho Sato-DahlmanDivision of Basic and Translational Research, Department of Surgery, University of Minnesota, MMC 195, 420 Delaware St SE, Minneapolis, MN 55455, USA.ORCID 0000-0003-2019-5557
Christopher J LaRoccaDivision of Basic and Translational Research, Department of Surgery, University of Minnesota, MMC 195, 420 Delaware St SE, Minneapolis, MN 55455, USA.ORCID 0000-0002-9808-1405
Chikako YanagibaDivision of Basic and Translational Research, Department of Surgery, University of Minnesota, MMC 195, 420 Delaware St SE, Minneapolis, MN 55455, USA.
Masato YamamotoDivision of Basic and Translational Research, Department of Surgery, University of Minnesota, MMC 195, 420 Delaware St SE, Minneapolis, MN 55455, USA.
University of Minnesota · US

Funding

Combination therapy with IFN expressing oncolytic adenovirus for pancreatic cancerR01CA228760 · NCI · UNIVERSITY OF MINNESOTA · PI DAVYDOVA, JULIA, YAMAMOTO, MASATO · 2019 to 2023
$1.7M
Systemic Therapy with Infectivity-Selective Oncolytic Adenovirus for PDACR01CA196215 · NCI · UNIVERSITY OF MINNESOTA · PI YAMAMOTO, MASATO · 2016 to 2020
$1.7M
Next Generation Oncolytic Adenovirus for Advanced Pancreatic Cancer TreatmentR01CA168448 · NCI · UNIVERSITY OF MINNESOTA · PI YAMAMOTO, MASATO · 2013 to 2017
$1.6M
NCI NIH HHS R01 CA168448NCI NIH HHS R01CA168448NCI NIH HHS R01 CA196215NCI NIH HHS R01CA196215NCI NIH HHS R01 CA228760NCI NIH HHS R01CA228760
6 · The paper itself

Abstract

Gene therapy with viral vectors has significantly advanced in the past few decades, with adenovirus being one of the most commonly employed vectors for cancer gene therapy. Adenovirus vectors can be divided into 2 groups: (1) replication-deficient viruses; and (2) replication-competent, oncolytic (OVs) viruses. Replication-deficient adenoviruses have been explored as vaccine carriers and gene therapy vectors. Oncolytic adenoviruses are designed to selectively target, replicate, and directly destroy cancer cells. Additionally, virus-mediated cell lysis releases tumor antigens and induces local inflammation (e.g., immunogenic cell death), which contributes significantly to the reversal of local immune suppression and development of antitumor immune responses ("cold" tumor into "hot" tumor). There is a growing body of evidence suggesting that the host immune response may provide a critical boost for the efficacy of oncolytic virotherapy. Additionally, genetic engineering of oncolytic viruses allows local expression of immune therapeutics, thereby reducing related toxicities. Therefore, the combination of oncolytic virus and immunotherapy is an attractive therapeutic strategy for cancer treatment. In this review, we focus on adenovirus-based vectors and discuss recent progress in combination therapy of adenoviruses with immunotherapy in preclinical and clinical studies.

Indexed as

adenovirus vectorCAR-T cell therapycheckpoint inhibitorimmunotherapyoncolytic adenovirus

Identifiers

PMID32455560
PMCPMC7281656
OpenAlexW3027914444

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.