Evidence map›Paper›PMID 35804841›Full record

ArticleCancers2022

Risk Factors and Clinicopathological Features for Developing a Subsequent Primary Cutaneous Squamous and Basal Cell Carcinomas.

Magdalena Ciążyńska, Marta Pabianek, Martyna Sławińska, Adam Reich, Bogumił Lewandowski, Katarzyna Szczepaniak, Małgorzata Ułańska, Dariusz Nejc, Robert Brodowski, Michał Sobjanek and 17 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 17 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

27 authors at 7 institutions in 1 country.

Magdalena CiążyńskaDepartment of Proliferative Diseases, Nicolaus Copernicus Multidisciplinary Centre for Oncology and Traumatology, ul. Pabianicka 62, 93-513 Lodz, Poland.ORCID 0000-0002-9709-3383
Marta PabianekDepartment of Proliferative Diseases, Nicolaus Copernicus Multidisciplinary Centre for Oncology and Traumatology, ul. Pabianicka 62, 93-513 Lodz, Poland.
Martyna SławińskaDepartment of Dermatology, Venereology and Allergology, Medical University of Gdansk, 80-214 Gdansk, Poland.
Adam ReichDepartment of Dermatology, University of Rzeszow, 35-310 Rzeszow, Poland.
Bogumił LewandowskiClinical Department of Maxillo-Facial Surgery, Frederic Chopin Provincial Specialist Hospital, 35-310 Rzeszow, Poland.
Katarzyna SzczepaniakDepartment of Proliferative Diseases, Nicolaus Copernicus Multidisciplinary Centre for Oncology and Traumatology, ul. Pabianicka 62, 93-513 Lodz, Poland.
Małgorzata UłańskaDepartment of Proliferative Diseases, Nicolaus Copernicus Multidisciplinary Centre for Oncology and Traumatology, ul. Pabianicka 62, 93-513 Lodz, Poland.
Dariusz NejcDepartment of Surgical Oncology, Medical University in Lodz, Nicolaus Copernicus Multidisciplinary Centre for Oncology and Traumatology, 93-513 Lodz, Poland.
Robert BrodowskiClinical Department of Maxillo-Facial Surgery, Frederic Chopin Provincial Specialist Hospital, 35-310 Rzeszow, Poland.
Michał SobjanekDepartment of Dermatology, Venereology and Allergology, Medical University of Gdansk, 80-214 Gdansk, Poland.
Witold OwczarekDermatology Clinic, Military Institute of Medicine in Warsaw, 04-141 Warsaw, Poland.
Grażyna Kamińska-WinciorekDepartment of Bone Marrow Transplantation and Hematology-Oncology, The Maria Skłodowska-Curie Memorial Cancer Centre and Institute of Oncology, Branch in Gliwice, 44-102 Gliwice, Poland.
Dariusz LangeDepartment of Tumor Pathology, The Maria Skłodowska-Curie Memorial Cancer Centre and Institute of Oncology, Branch in Gliwice, 44-102 Gliwice, Poland.
Monika SłowińskaDermatology Clinic, Military Institute of Medicine in Warsaw, 04-141 Warsaw, Poland.
Katarzyna WróbelDermatology Clinic, Military Institute of Medicine in Warsaw, 04-141 Warsaw, Poland.
Andrzej BieniekBieniek Medical Center, 52-016 Wrocław, Poland.
Anna WoźniackaDepartment of Dermatology and Venereology, Medical University of Lodz, 90-419 Lodz, Poland.
Anika PękalaDepartment of Proliferative Diseases, Nicolaus Copernicus Multidisciplinary Centre for Oncology and Traumatology, ul. Pabianicka 62, 93-513 Lodz, Poland.
Łukasz KuncmanDepartment of Radiotherapy, Medical University of Lodz, 93-513 Lodz, Poland.
Magdalena SalińskaDepartment of Dermatology and Venereology, Medical University of Lodz, 90-419 Lodz, Poland.
Marcin NowetaDepartment of Dermatology, Paediatric Dermatology and Oncology Clinic, Medical University of Lodz, 91-347 Lodz, Poland.
Małgorzata SkibińskaDepartment of Dermatology, Paediatric Dermatology and Oncology Clinic, Medical University of Lodz, 91-347 Lodz, Poland.
Joanna NarbuttDepartment of Dermatology, Paediatric Dermatology and Oncology Clinic, Medical University of Lodz, 91-347 Lodz, Poland.
Karol CiążyńskiInstitute of Applied Computer Science, Lodz University of Technology, 90-537 Lodz, Poland.
Marta LewandowskaDepartment of Infectious Diseases and Hepatology for Adults, Medical University of Lodz, 93-513 Lodz, Poland.
Elżbieta Dziankowska-ZaborszczykDepartment of Epidemiology and Biostatistics, Medical University of Lodz, 90-419 Lodz, Poland.
Aleksandra LesiakDepartment of Dermatology, Paediatric Dermatology and Oncology Clinic, Medical University of Lodz, 91-347 Lodz, Poland.
Medical University of Lodz · PLCopernicus Memorial Hospital · PLWojskowy Instytut Medycyny Lotniczej · PLGdańsk Medical University · PLThe Maria Sklodowska-Curie National Research Institute of Oncology · PLLodz University of Technology · PLUniversity of Rzeszów · PL

Funding

Medical University of Lodz 503/5‑064‑01/503‑1National Centre of Science 2017/27/B/NZ5/02011
6 · The paper itself

Abstract

backgroundPatients with diagnosed keratinocyte carcinomas (KCs) have an increased risk of subsequent skin cancers development. Current studies indicate that patients with subsequent tumors should be followed up regularly. However, none of the studies indicate the connection between the specific subtypes and an increased risk for further KCs development. The study assesses the differences in the risk of developing a subsequent skin cancer after a previous diagnosis of KC, especially considering individual types of skin malignances, and identifies potential factors associated with an increased risk of new cutaneous tumor describing non-invasive diagnosis and monitoring.

methodsPathology and medical records were examined to identify the characteristics of patients with multiple KCs diagnosed between 1999 and 2019.

resultsThe study group comprised 13,913 KCs occurring in 10,083 patients. Multiple KCs were observed in 2300 patients (22.8%). The analysis showed aggressive subtypes, multiple tumors, and male sex as significant prognostic factors.

conclusionsThe most crucial risk factors for developing subsequent KC are being of a male gender, an aggressive tumor subtype, and previous history of multiple skin cancers. Basal cell carcinoma subtypes, such as infiltrative basosquamous, with aggressive growth patterns predispose not only to increased risk for the recurrence but are also expected to be at higher risk of subsequent KCs.

Indexed as

basal cell carcinomakeratinocyte carcinomasnon-invasive diagnosis and monitoringnon-melanoma skin cancersquamous cell carcinoma

Identifiers

PMID35804841
PMCPMC9264931
OpenAlexW4283316068

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Registered trials

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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.