Evidence map›Paper›PMID 42200833›Full record

ArticleAntibodies (Basel, Switzerland)2026

Immune-Related Adverse Events of Cemiplimab Therapy in Advanced Cervical Cancer-Data from the Polish-Czech Cervical Cancer Immunotherapy Group (PCCIG-01) with a Review of the Literature.

Radosław Łupkowski, Karolina Górniak, Maja Lisik-Habib, Ewa Burchardt, Radosław Mądry, Monika Szarszewska, Katarzyna Gabalewicz, Dominika Pyszak, Petra Bretova, Beata Maćkowiak-Matejczyk and 10 more

Abstract read
In one paragraph

Article in Antibodies (Basel, Switzerland), 2026. 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
–field-weighted citation impact
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.

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

20 authors.

Radosław ŁupkowskiDepartment of Gynecological Oncology, Krakow Branch, Maria Sklodowska-Curie National Research Institute of Oncology, Garncarska 11 Street, 31-115 Krakow, Poland.
Karolina GórniakDepartment of Gynecological Oncology, Krakow Branch, Maria Sklodowska-Curie National Research Institute of Oncology, Garncarska 11 Street, 31-115 Krakow, Poland.
Maja Lisik-HabibDepartment of Proliferative Diseases, Comprehensive Oncology and Traumatology Center, Copernicus Memorial Hospital, 93-513 Lodz, Poland.
Ewa BurchardtDepartment of Radiotherapy and Gynaecological Oncology, Greater Poland Cancer Center in Poznan, 61-866 Poznań, Poland.ORCID 0000-0003-0497-637X
Radosław MądryDepartment of Oncology and Gynecological Oncology, Poznan University of Medical Sciences, 61-701 Poznań, Poland.
Monika SzarszewskaDepartment of Oncology and Gynecological Oncology, Poznan University of Medical Sciences, 61-701 Poznań, Poland.
Katarzyna GabalewiczLower Silesian Oncology, Pulmonology and Hematology Center, 53-413 Wrocław, Poland.ORCID 0000-0003-2435-827X
Dominika Pyszak3rd Clinic of Radiotherapy and Chemotherapy, Gliwice Branch, Maria Sklodowska-Curie National Research Institute of Oncology, 00-001 Warszawa, Poland.
Petra BretovaDepartment of Obstetrics and Gynecology, Faculty of Medicine, Charles University in Hradec Kralove, 500 03 Hradec Králové, Czech Republic.ORCID 0000-0003-1082-433X
Beata Maćkowiak-MatejczykDepartment of Gynaecological Oncology, Maria Sklodowska-Curie Bialystok Oncology Centre, 15-027 Białystok, Poland.
Wioletta SawczukDepartment of Gynaecological Oncology, Maria Sklodowska-Curie Bialystok Oncology Centre, 15-027 Białystok, Poland.ORCID 0009-0006-5586-5281
Monika Łączyńska-MaderaDepartment of Gynecology, Gynecology Oncology and Obstetrics, Fryderyk Chopin University Hospital in Rzeszów, 35-055 Rzeszów, Poland.
Dagmara Klasa-MazurkiewiczDepartment of Gynecology, Obstetrics, Gynecologic Oncology and Gynecologic Endocrinology, Medical University of Gdańsk, University Clinical Center, 80-952 Gdańsk, Poland.ORCID 0000-0003-0122-9504
Angelika Gawlik-UrbanDepartment of Gynecological Oncology, Krakow Branch, Maria Sklodowska-Curie National Research Institute of Oncology, Garncarska 11 Street, 31-115 Krakow, Poland.
Magdalena MichalikDepartment of Clinical Oncology, Prof. Kornel Gibiński University Clinical Center, Medical University of Silesia in Katowice, 40-055 Katowice, Poland.
Zuzanna BorysiewiczDepartment of Oncology and Chemotherapy, Provincial Integrated Hospital in Elbląg, 82-300 Elbląg, Poland.
Ewa IwańskaDepartment of Gynecological Oncology, Krakow Branch, Maria Sklodowska-Curie National Research Institute of Oncology, Garncarska 11 Street, 31-115 Krakow, Poland.ORCID 0000-0001-8597-1989
Mirosława PuskulluogluDepartment of Clinical Oncology, Krakow Branch, Maria Sklodowska-Curie National Research Institute of Oncology, 00-001 Warszawa, Poland.ORCID 0000-0002-2647-9625
Paweł BlecharzDepartment of Gynecological Oncology, Krakow Branch, Maria Sklodowska-Curie National Research Institute of Oncology, Garncarska 11 Street, 31-115 Krakow, Poland.
Renata Pacholczak-MadejDepartment of Gynecological Oncology, Krakow Branch, Maria Sklodowska-Curie National Research Institute of Oncology, Garncarska 11 Street, 31-115 Krakow, Poland.ORCID 0000-0002-6535-4841

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmunotherapy has become an integral part of systemic treatment for cervical cancer (CC). This study assessed the safety profile of cemiplimab and the association between immune-related adverse events (irAEs) and treatment outcomes in patients with persistent, recurrent or metastatic CC.

methodsThis ambispective, multicenter, real-world cohort study included 101 patients treated in 13 reference oncology centers as part of the PCCIG-01 study. We evaluated the frequency and severity of irAEs and their association with progression-free survival (PFS) and overall survival (OS). Survival outcomes were analyzed using the Kaplan-Meier method and Cox proportional hazards models, with

resultsAfter a median follow-up of 7.5 months, adverse events occurred in 45 patients (44.6%) and were mostly grade (G) 1-2. IrAEs were observed in 34 patients (33.7%). Endocrine toxicities predominated (

conclusionsIn exploratory analyses, the occurrence of irAEs was associated with improved PFS in cemiplimab-treated patients with persistent, recurrent or metastatic CC. Cemiplimab showed a manageable safety profile, with most toxicities being G1-G2.

Indexed as

adverse eventscemiplimabcervical cancerimmune checkpoint inhibitorsPD-1/PD-L1

Identifiers

PMID42200833
PMCPMC13214483

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