Evidence map›Paper›PMID 35634282›Full record

ArticleFrontiers in immunology2022

Comprehensive Testing of Chemotherapy and Immune Checkpoint Blockade in Preclinical Cancer Models Identifies Additive Combinations.

Nicola Principe, Wayne J Aston, Danika E Hope, Caitlin M Tilsed, Scott A Fisher, Louis Boon, Ian M Dick, Wee Loong Chin, Alison M McDonnell, Anna K Nowak and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  3. Modeling combination chemo-immunotherapy for heterogeneous tumors.Quantitative biology (Beijing, China) · 2025
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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

13 authors at 3 institutions in 1 country.

Nicola PrincipeNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, WA, Australia.
Wayne J AstonNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, WA, Australia.
Danika E HopeNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, WA, Australia.
Caitlin M TilsedNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, WA, Australia.
Scott A FisherNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, WA, Australia.
Louis BoonJJP Biologics, Warsaw, Poland.
Ian M DickNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, WA, Australia.
Wee Loong ChinNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, WA, Australia.
Alison M McDonnellTelethon Kids Institute, Perth, WA, Australia.
Anna K NowakNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, WA, Australia.
Richard A LakeNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, WA, Australia.
Jonathan CheeNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, WA, Australia.
Willem Joost LesterhuisNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, WA, Australia.
University of Western Australia · AUInstitute for Respiratory Health · AUThe Kids Research Institute Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibodies that target immune checkpoints such as cytotoxic T lymphocyte antigen 4 (CTLA-4) and the programmed cell death protein 1/ligand 1 (PD-1/PD-L1) are now a treatment option for multiple cancer types. However, as a monotherapy, objective responses only occur in a minority of patients. Chemotherapy is widely used in combination with immune checkpoint blockade (ICB). Although a variety of isolated immunostimulatory effects have been reported for several classes of chemotherapeutics, it is unclear which chemotherapeutics provide the most benefit when combined with ICB. We investigated 10 chemotherapies from the main canonical classes dosed at the clinically relevant maximum tolerated dose in combination with anti-CTLA-4/anti-PD-L1 ICB. We screened these chemo-immunotherapy combinations in two murine mesothelioma models from two different genetic backgrounds, and identified chemotherapies that produced additive, neutral or antagonistic effects when combined with ICB. Using flow cytometry and bulk RNAseq, we characterized the tumor immune milieu in additive chemo-immunotherapy combinations. 5-fluorouracil (5-FU) or cisplatin were additive when combined with ICB while vinorelbine and etoposide provided no additional benefit when combined with ICB. The combination of 5-FU with ICB augmented an inflammatory tumor microenvironment with markedly increased CD8

Indexed as

Immune Checkpoint InhibitorsNeoplasmsAnimalsCD8-Positive T-LymphocytesFluorouracilHumansMiceTumor MicroenvironmentTumor Necrosis Factor-alphaFluorouracilImmune Checkpoint InhibitorsTumor Necrosis Factor-alphachemo-immunotherapy combinationscisplatinfluorouracil (5-FU)IL-1bimmune checkpoint blockade (ICB) therapyproinflammatory cytokineT cellsTNFa = tumor necrosis factor–a

Identifiers

PMID35634282
PMCPMC9132586
OpenAlexW4280596001

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.