Evidence map›Paper›PMID 38025838›Full record

ArticleOncoimmunology2023

Emergence of immune-related adverse events correlates with pathological complete response in patients receiving pembrolizumab for early triple-negative breast cancer.

Maximilian Marhold, Simon Udovica, Anna Halstead, Mona Hirdler, Muna Ferner, Kerstin Wimmer, Zsuzsanna Bago-Horvath, Ruth Exner, Florian Fitzal, Kathrin Strasser-Weippl and 2 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.5field-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

27 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

12 authors at 2 institutions in 2 countries.

Maximilian MarholdDivision of Oncology, Department for Medicine I, Medical University of Vienna, Vienna, Austria.
Simon UdovicaDepartment of Medicine I, Center for Oncology and Hematology, Clinic Ottakring, Vienna, Austria.
Anna HalsteadBristol Medical School, University of Bristol, Bristol, UK.
Mona HirdlerDepartment of Internal Medicine I for Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Linz, Austria.
Muna FernerDepartment of Medicine I, Center for Oncology and Hematology, Clinic Ottakring, Vienna, Austria.
Kerstin WimmerDepartment of General Surgery, Medical University of Vienna, Vienna, Austria.
Zsuzsanna Bago-HorvathInstitute for Pathology, Medical University of Vienna, Vienna, Austria.
Ruth ExnerDepartment of General Surgery, Medical University of Vienna, Vienna, Austria.
Florian FitzalDepartment of General Surgery, Medical University of Vienna, Vienna, Austria.
Kathrin Strasser-WeipplDepartment of Medicine I, Center for Oncology and Hematology, Clinic Ottakring, Vienna, Austria.
Tim RobinsonBristol Medical School, University of Bristol, Bristol, UK.
Rupert BartschDivision of Oncology, Department for Medicine I, Medical University of Vienna, Vienna, Austria.
Medical University of Vienna · ATUniversity of Bristol · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Based upon results of the KEYNOTE-522 trial and following approval by regulatory authorities, the addition of pembrolizumab to chemotherapy is now the standard-of-care for the treatment of early triple-negative breast cancer (eTNBC) (Clinical stage II-III). Pembrolizumab is a programmed cell death protein 1 monoclonal antibody, known to cause immune-related adverse events (irAEs) in a significant subset of patients. Real-world data on incidence, type and treatment strategies of irAEs in the setting of eTNBC treatment are sparse. In this multicenterretrospective analysis, we characterized real-world incidence of irAEs and treatment outcomes such as pathological complete response (pCR) from the combination of pembrolizumab and chemotherapy as neoadjuvant treatment for eTNBC. We found a rate of irAEs of all grades of 63.9% and of 20% for irAEs of grade 3 or higher. In the overall population, a pCR rate of 57.1% was observed. The emergence of irAEs correlated significantly with pCR (72.2% versus 30.8%;

Indexed as

Triple Negative Breast NeoplasmsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedHumansTreatment OutcomeAntibodies, MonoclonalAntibodies, Monoclonal, Humanizedpembrolizumabcheckpoint inhibitionEarly triple negative breast cancerneoadjuvantpembrolizumab

Identifiers

PMID38025838
PMCPMC10653620
OpenAlexW4388638630

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.