How to classify, diagnose, treat and follow-up extragonadal germ cell tumors? A systematic review of available evidence.


Journal

World journal of urology
ISSN: 1433-8726
Titre abrégé: World J Urol
Pays: Germany
ID NLM: 8307716

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 03 07 2021
accepted: 01 02 2022
pubmed: 14 5 2022
medline: 3 12 2022
entrez: 13 5 2022
Statut: ppublish

Résumé

To present the current evidence and the development of studies in recent years on the management of extragonadal germ cell tumors (EGCT). A systematic literature search was conducted in Medline and the Cochrane Library. Studies within the search period (January 2010 to February 2021) that addressed the classification, diagnosis, prognosis, treatment, and follow-up of extragonadal tumors were included. Risk of bias was assessed and relevant data were extracted in evidence tables. The systematic search identified nine studies. Germ cell tumors (GCT) arise predominantly from within the testis, but about 5% of the tumors are primarily located extragonadal. EGCT are localized primarily mediastinal or retroperitoneal in the midline of the body. EGCT patients are classified according to the IGCCCG classification. Consecutively, all mediastinal non-seminomatous EGCT patients belong to the "poor prognosis" group. In contrast mediastinal seminoma and both retroperitoneal seminoma and non-seminoma patients seem to have a similar prognosis as patients with gonadal GCTs and metastasis at theses respective sites. The standard chemotherapy regimen for patients with a EGCT consists of 3-4 cycles (good vs intermediate prognosis) of bleomycin, etoposid, cisplatin (BEP); however, due to their very poor prognosis patients with non-seminomatous mediastinal GCT should receive a dose-intensified or high-dose chemotherapy approach upfront on an individual basis and should thus be referred to expert centers Ifosfamide may be exchanged for bleomycin in cases of additional pulmonary metastasis due to subsequently planned resections. In general patients with non-seminomatous EGCT, residual tumor resection (RTR) should be performed after chemotherapy. In general, non-seminomatous EGCT have a poorer prognosis compared to testicular GCT, while seminomatous EGGCT seem to have a similar prognosis to patients with metastatic testicular seminoma. The current insights on EGCT are limited, since all data are mainly based on case series and studies with small patient numbers and non-comparative studies. In general, systemic treatment should be performed like in testicular metastatic GCTs but upfront dose intensification of chemotherapy should be considered for mediastinal non-seminoma patients. Thus, EGCT should be referred to interdisciplinary centers with utmost experience in the treatment of germ cell tumors.

Identifiants

pubmed: 35554637
doi: 10.1007/s00345-022-04009-z
pii: 10.1007/s00345-022-04009-z
pmc: PMC9712285
doi:

Substances chimiques

Bleomycin 11056-06-7

Types de publication

Systematic Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2863-2878

Informations de copyright

© 2022. The Author(s).

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Auteurs

Christian Winter (C)

Urological Practice "Urologie Neandertal", Erkrath, Germany. christian.winter@med.uni-duesseldorf.de.
Department of Urology, University Hospital Düsseldorf, Medical Faculty, Heinrich-Heine University, Düsseldorf, Germany. christian.winter@med.uni-duesseldorf.de.

Friedemann Zengerling (F)

Department of Urology and Pediatric Urology, University Hospital of Ulm, Ulm, Germany.
UroEvidence@Deutsche Gesellschaft Für Urologie, Berlin, Germany.

Jonas Busch (J)

Department of Urology, Charité Universitaetsmedizin Berlin, Berlin, Germany.

Julia Heinzelbecker (J)

Department of Urology and Paediatric Urology, Saarland University Medical Centre, Faculty of Medicine, Saarland University, Homburg, Saar, Germany.

David Pfister (D)

Department of Urology, University Hospital Cologne, Cologne, Germany.

Christian Ruf (C)

Department of Urology, Bundeswehrkrankenhaus, Ulm, Germany.

Julia Lackner (J)

UroEvidence@Deutsche Gesellschaft Für Urologie, Berlin, Germany.

Peter Albers (P)

Department of Urology, University Hospital Düsseldorf, Medical Faculty, Heinrich-Heine University, Düsseldorf, Germany.

Sabine Kliesch (S)

Centre of Reproductive Medicine and Andrology, Department of Clinical and Surgical Andrology, University Hospital, Münster, Münster, Germany.

Stefanie Schmidt (S)

Department of Urology and Pediatric Urology, University Hospital of Ulm, Ulm, Germany.

Carsten Bokemeyer (C)

Department of Oncology, Hematology, BMT Plus Section Pneumology, University Cancer Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

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