Evaluation of Prognostic Parameters to Identify Aggressive Penile Carcinomas.

HPV histological subtype p16 penile cancer prognosis

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
27 Sep 2023
Historique:
received: 29 08 2023
revised: 11 09 2023
accepted: 20 09 2023
medline: 14 10 2023
pubmed: 14 10 2023
entrez: 14 10 2023
Statut: epublish

Résumé

Advanced penile carcinoma is characterized by poor prognosis. Most data on prognostic factors are based on small study cohorts, and even meta-analyses are limited in patient numbers. Therefore, there is still a lack of evidence for clinical decisions. In addition, the most recent TNM classification is questionable; in line with previous studies, we found that it has not improved prognosis estimation. We evaluated 297 patients from Germany, Russia, and Portugal. Tissue samples from 233 patients were re-analyzed by two experienced pathologists. HPV status, p16, and histopathological parameters were evaluated for all patients. Advanced lymph node metastases (N2, N3) were highly significantly associated with reductions in metastasis-free (MFS), cancer-specific (CS), and overall survival (OS) rates ( Lymphatic involvement has the highest impact on prognosis in penile cancer, whereas HPV status alone is not suitable as a prognostic parameter. The pT1b stage, which includes grading, as well as lymphovascular and perineural invasion in the T stage, seems questionable; a revision of the TNM classification is therefore required.

Sections du résumé

BACKGROUND BACKGROUND
Advanced penile carcinoma is characterized by poor prognosis. Most data on prognostic factors are based on small study cohorts, and even meta-analyses are limited in patient numbers. Therefore, there is still a lack of evidence for clinical decisions. In addition, the most recent TNM classification is questionable; in line with previous studies, we found that it has not improved prognosis estimation.
METHODS METHODS
We evaluated 297 patients from Germany, Russia, and Portugal. Tissue samples from 233 patients were re-analyzed by two experienced pathologists. HPV status, p16, and histopathological parameters were evaluated for all patients.
RESULTS RESULTS
Advanced lymph node metastases (N2, N3) were highly significantly associated with reductions in metastasis-free (MFS), cancer-specific (CS), and overall survival (OS) rates (
CONCLUSION CONCLUSIONS
Lymphatic involvement has the highest impact on prognosis in penile cancer, whereas HPV status alone is not suitable as a prognostic parameter. The pT1b stage, which includes grading, as well as lymphovascular and perineural invasion in the T stage, seems questionable; a revision of the TNM classification is therefore required.

Identifiants

pubmed: 37835442
pii: cancers15194748
doi: 10.3390/cancers15194748
pmc: PMC10571727
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Jan Niklas Mink (JN)

Department of Urology and Paediatric Urology, Saarland University, 66421 Homburg, Germany.

Oybek Khalmurzaev (O)

Department of Urology and Paediatric Urology, Saarland University, 66421 Homburg, Germany.
Department of Urology, Federal State Budgetary Institution "N.N. Blokhin National Medical Research Center of Oncology", Ministry of Health of the Russian Federation, Moscow 115478, Russia.

Alexey Pryalukhin (A)

Institute of Pathology, Saarland University Medical Centre, 66421 Homburg, Germany.

Carol Immanuel Geppert (CI)

Institute of Pathology, University Erlangen-Nuremberg, 91054 Erlangen, Germany.

Stefan Lohse (S)

Institute of Virology, Saarland University, 66123 Homburg, Germany.

Kristof Bende (K)

Institute of Pathology, University Erlangen-Nuremberg, 91054 Erlangen, Germany.

João Lobo (J)

Department of Pathology and Cancer Biology and Epigenetics Group-Research Center, Portuguese Oncology Institute of Porto/Porto Comprehensive Cancer Center Raquel Seruca, School of Medicine and Biomedical Sciences (ICBAS), University of Porto, 4050-513 Porto, Portugal.

Rui Henrique (R)

Department of Pathology and Cancer Biology and Epigenetics Group-Research Center, Portuguese Oncology Institute of Porto/Porto Comprehensive Cancer Center Raquel Seruca, School of Medicine and Biomedical Sciences (ICBAS), University of Porto, 4050-513 Porto, Portugal.

Hagen Loertzer (H)

Clinic of Urology and Paediatric Urology, Westpfalz-Klinikum, 67655 Kaiserslautern, Germany.

Joachim Steffens (J)

Department of Urology and Paediatric Urology, St. Antonius Hospital, 52249 Eschweiler, Germany.

Carmen Jerónimo (C)

Department of Pathology and Cancer Biology and Epigenetics Group-Research Center, Portuguese Oncology Institute of Porto/Porto Comprehensive Cancer Center Raquel Seruca, School of Medicine and Biomedical Sciences (ICBAS), University of Porto, 4050-513 Porto, Portugal.

Heiko Wunderlich (H)

Clinic of Urology and Paediatric Urology, St. Georg Klinikum, 99817 Eisenach, Germany.

Julia Heinzelbecker (J)

Department of Urology and Paediatric Urology, Saarland University, 66421 Homburg, Germany.

Rainer M Bohle (RM)

Institute of Pathology, Saarland University Medical Centre, 66421 Homburg, Germany.

Michael Stöckle (M)

Department of Urology and Paediatric Urology, Saarland University, 66421 Homburg, Germany.

Vsevolod Matveev (V)

Department of Urology, Federal State Budgetary Institution "N.N. Blokhin National Medical Research Center of Oncology", Ministry of Health of the Russian Federation, Moscow 115478, Russia.

Arndt Hartmann (A)

Institute of Pathology, University Erlangen-Nuremberg, 91054 Erlangen, Germany.

Kerstin Junker (K)

Department of Urology and Paediatric Urology, Saarland University, 66421 Homburg, Germany.

Classifications MeSH