Evidence map›Paper›PMID 37794264›Full record

ArticleCancer immunology, immunotherapy : CII2023

Toxicity-specific peripheral blood T and B cell dynamics in anti-PD-1 and combined immune checkpoint inhibition.

Mick J M van Eijs, Rik J Verheijden, Stefanie A van der Wees, Stefan Nierkens, Anne S R van Lindert, Karijn P M Suijkerbuijk, Femke van Wijk, UNICIT consortium

Open access · hybridAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

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  12. Serum cytokines and creatinine/cystatin C ratio as prognostic biomarkers in advanced cancer patients treated with anti-PD-1/PD-L1 therapy.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2024
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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

8 authors at 1 institution in 1 country.

Mick J M van EijsDepartment of Medical Oncology, University Medical Center Utrecht, KC.02.085.2, P.O. Box 85090, 3508 AB, Utrecht, the Netherlands. m.j.m.vaneijs-2@umcutrecht.nl.ORCID http://orcid.org/0000-0002-9763-6704
Rik J VerheijdenDepartment of Medical Oncology, University Medical Center Utrecht, KC.02.085.2, P.O. Box 85090, 3508 AB, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0003-1966-1063
Stefanie A van der WeesCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, the Netherlands.
Stefan NierkensCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0003-3406-817X
Anne S R van LindertDepartment of Pulmonology, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-4072-2441
Karijn P M Suijkerbuijk *Department of Medical Oncology, University Medical Center Utrecht, KC.02.085.2, P.O. Box 85090, 3508 AB, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0003-3604-5430
Femke van Wijk *Center for Translational Immunology, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0001-8343-1356
UNICIT consortium
University Medical Center Utrecht · NL

Funding

Bristol-Myers Squibb CA209-6JY
6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICI) have revolutionized the treatment landscape of advanced malignancies, but come with a diverse spectrum of immune-related adverse events (irAEs). Mechanistic studies can aid the transition from expert-opinion to evidence-based irAE treatment strategies. We aimed to longitudinally characterize peripheral blood T and B cell dynamics in ICI-treated patients by multicolor flow cytometry and serum multiplex immunoassay at baseline, ± 3 weeks and ± 6 weeks or upon clinically relevant irAEs. We analyzed samples from 44 ICI-treated patients (24 anti-PD-1 monotherapy, 20 combined anti-PD-1/anti-CTLA-4; cICI), of whom 21 developed irAEs, and 10 healthy donors. IrAEs after cICI were characterized by significantly enhanced proliferation of Th1-associated, mainly (CD4

Indexed as

Antineoplastic AgentsAntineoplastic Agents, ImmunologicalNeoplasmsCD8-Positive T-LymphocytesHumansImmune Checkpoint InhibitorsAntineoplastic AgentsAntineoplastic Agents, ImmunologicalImmune Checkpoint InhibitorsImmune checkpoint inhibitorsImmune-related adverse eventPeripheral blood, immunophenotypingT and B lymphocytes

Identifiers

PMID37794264
PMCPMC10700442
OpenAlexW4387344629

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.