Evidence map›Paper›PMID 35968405›Full record

ArticleOncoimmunology2022

Synergistic effect of combining sunitinib with a peptide-based vaccine in cancer treatment after microenvironment remodeling.

Alice Mougel, Fanny Méjean, Thi Tran, Yasmine Adimi, Isabelle Galy-Fauroux, Christelle Kaboré, Erwan Mercier, Pauline Urquia, Magali Terme, Eric Tartour and 1 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. 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

11 authors at 1 institution in 1 country.

Alice MougelUniversité Paris Cité, Inserm, PARCC, F-75015 Paris, France.
Fanny MéjeanUniversité Paris Cité, Inserm, PARCC, F-75015 Paris, France.
Thi TranUniversité Paris Cité, Inserm, PARCC, F-75015 Paris, France.
Yasmine AdimiUniversité Paris Cité, Inserm, PARCC, F-75015 Paris, France.
Isabelle Galy-FaurouxUniversité Paris Cité, Inserm, PARCC, F-75015 Paris, France.
Christelle KaboréUniversité Paris Cité, Inserm, PARCC, F-75015 Paris, France.
Erwan MercierUniversité Paris Cité, Inserm, PARCC, F-75015 Paris, France.
Pauline UrquiaUniversité Paris Cité, Inserm, PARCC, F-75015 Paris, France.
Magali TermeUniversité Paris Cité, Inserm, PARCC, F-75015 Paris, France.
Eric TartourUniversité Paris Cité, Inserm, PARCC, F-75015 Paris, France.
Corinne TanchotUniversité Paris Cité, Inserm, PARCC, F-75015 Paris, France.ORCID 0000-0002-2913-1755
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although it has proven difficult to demonstrate the clinical efficacy of therapeutic vaccination as a monotherapy in advanced cancers, its combination with an immunomodulatory treatment to reduce intra-tumor immunosuppression and improve vaccine efficacy is a very promising strategy. In this context, we are studying the combination of a vaccine composed of peptides of the tumor antigen survivin (SVX vaccine) with the anti-angiogenic agent sunitinib in a colorectal carcinoma model. To this end, we have been focusing on administration scheduling and have highlighted a therapeutic synergy between SVX vaccine and sunitinib when the vaccine was administered at the end of anti-angiogenic treatment. In this setting, a prolonged control of tumor growth associated with an important percentage of complete tumor regression was observed. Studying the remodeling induced by each therapy on the immunological and angiogenic tumor microenvironment over time we observed, during sunitinib treatment, a transient increase in polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs) and a decrease in NK cells in the tumor microenvironment. In contrast, after sunitinib treatment was stopped, a decrease in PMN-MDSC populations has been observed in the tumor, associated with an increase in NK cells, pericyte coverage of tumor vessels and CD8

Indexed as

ImmunotherapyNeoplasmsHumansSunitinibTumor MicroenvironmentVaccines, SubunitSunitinibVaccines, Subunitanti-angiogenic treatmentcancer vaccineCD8+ T cell infiltrateMDSCsNK cellsTherapeutic combinationstumor microenvironment

Identifiers

PMID35968405
PMCPMC9367646
OpenAlexW4297816424

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.