Evidence map›Paper›PMID 32152702›Full record

ArticleCancer immunology, immunotherapy : CII2020

Significant association between tumor mutational burden and immune-related adverse events during immune checkpoint inhibition therapies.

Csaba Kerepesi, Tibor Bakacs, Ralph W Moss, Shimon Slavin, Colin C Anderson

Open access · hybridAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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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

5 authors at 3 institutions in 4 countries.

Csaba KerepesiInstitute for Computer Science and Control (SZTAKI), Kende u 13-17, Budapest, 1111, Hungary. kerepesi@sztaki.hu.
Tibor BakacsPRET Therapeutics Ltd., Budapest, 1124, Hungary.
Ralph W MossMoss Reports, 104 Main Street Unit 1422, Blue Hill, ME, 04614-1422, USA.
Shimon SlavinBiotherapy International, The Center for Innovative Cancer Immunotherapy and Cellular Medicine, Weizmann Center, 14 Weizmann Street Floor 15, Suite 1503, 64239, Tel Aviv, Israel.
Colin C AndersonDepartments of Surgery and Medical Microbiology and Immunology, Alberta Diabetes Institute, Alberta Transplant Institute, University of Alberta, Edmonton, AB, T6G 2E1, Canada. colinand@ualberta.ca.ORCID http://orcid.org/0000-0003-1733-4237
Brigham and Women's Hospital · USUniversity of Alberta · CAWeizmann Institute of Science · IL

Funding

CIHR PS148588Ministry of Human Capacities in Hungary 2018-1.2.1-NKP-00008
6 · The paper itself

Abstract

More than 2000 immuno-oncology agents are being tested or are in use as a result of the cancer immunotherapy revolution. Manipulation of co-inhibitory receptors has achieved tumor eradication in a minority of patients, but widespread immune-related adverse events (irAEs) compromised tolerance to healthy self-tissues in the majority. We have proposed that a major mechanism of irAEs is similar to a graft-versus-malignancy effect of graft-versus-host disease. To verify our hypothesis, we retrieved post-marketing data of adverse events from the U.S. Food and Drug Administration Adverse Event Reporting System. A significant positive correlation was revealed in 7677 patients between the reporting odds ratio of irAEs during immune checkpoint inhibitor therapy and the corresponding tumor mutational burden across 19 cancer types. These results can be interpreted to mean that the ICI drugs unleashed T cells against "altered-self," self, and tumors resulting in better overall survival.

Indexed as

Adverse Drug Reaction Reporting SystemsAntigens, NeoplasmAntineoplastic Agents, ImmunologicalDrug-Related Side Effects and Adverse ReactionsHumansMutationNeoplasmsSelf ToleranceT-LymphocytesAntigens, NeoplasmAntineoplastic Agents, ImmunologicalFAERSGraft-versus-host diseaseImmune checkpoint inhibitionImmune-related adverse eventTumor mutation burden

Identifiers

PMID32152702
PMCPMC7183506
OpenAlexW3010582098

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.