Evidence map›Paper›PMID 38405211›Full record

ArticleContemporary oncology (Poznan, Poland)2023

First experience in treating advanced urothelial cancer with enfortumab vedotin. Single-centre retrospective study of patients qualified for a rescue access procedure.

Bożena Sikora-Kupis, Piotr Domański, Weronika Fortuniak, Barbara Kruczyk, Szymon Staneta, Mateusz Piętak, Anna Mydlak, Tomasz Demkow, Paulina Dumnicka, Jakub Kucharz

Open access · goldAbstract read
In one paragraph

Article in Contemporary oncology (Poznan, Poland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 2 institutions in 1 country.

Bożena Sikora-KupisDepartment of Uro-Oncology, Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Piotr DomańskiDepartment of Uro-Oncology, Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Weronika FortuniakDepartment of Uro-Oncology, Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Barbara KruczykDepartment of Uro-Oncology, Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Szymon StanetaDepartment of Uro-Oncology, Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Mateusz PiętakDepartment of Uro-Oncology, Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Anna MydlakDepartment of Head and Neck Oncology, Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Tomasz DemkowDepartment of Uro-Oncology, Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Paulina DumnickaChair of Biochemistry, Jagiellonian University Medical College, Kraków, Poland.
Jakub KucharzDepartment of Uro-Oncology, Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
The Maria Sklodowska-Curie National Research Institute of Oncology · PLJagiellonian University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Urothelial carcinoma is the most common type of urinary tract malignancy. Current treatment options, including platinum-based chemotherapy or immunotherapy, present significant challenges, ranging from limited efficacy to severe toxicities. Recent developments in antibody-drug conjugates (ADC), such as enfortumab vedotin (EV), promise to significantly improve overall survival. The study aims to evaluate the efficacy and tolerability of EV. In addition, we highlight the observed benefits of next-line treatment after progression. Material and methods: This retrospective study involved 16 patients with advanced urothelial cancer treated with EV at the Department of Genitourinary Oncology, Maria Skłodowska- Curie National Research Institute of Oncology between November 2022 and November 2023. The study evaluated patients' medical history, response to EV treatment, and side effects. Notably, the study included patients who had already exhausted standard treatment options and who were treated with EV through a rescue access procedure. Results: Partial response was observed in 4 out of 9 (44%) patients with available imaging. Common terminology criteria for adverse events (AE) grade 3 and 4 were observed in 3 out of 16 patients, which subsequently required dose reduction. Conclusions: Enfortumab vedotin demonstrates effectiveness in real-world settings in treating advanced urothelial cancer. Proper management of AE in experienced centres may further prolong survival. Personalized treatment and the development of new ADC represent the future for improved patient outcomes.

Indexed as

advanced urothelial cancerantibody-drug conjugates (ADC)enfortumab vedotin (EV)toxicity

Identifiers

PMID38405211
PMCPMC10883191
OpenAlexW4391665729

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.