Somatic Transformation in Metastatic Testicular Germ Cell Tumours - A Different Disease Entity.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 14 07 2019
revised: 22 07 2019
accepted: 23 07 2019
entrez: 15 9 2019
pubmed: 15 9 2019
medline: 27 9 2019
Statut: ppublish

Résumé

The occurrence of somatic transformation in germ cell tumour (GCT) is rare, with increased incidence in teratomatous tumours. The aim of this study was to understand the clinical outcomes of patients with metastatic GCT with somatic transformation. A retrospective study was conducted in two tertiary cancer centres in London. Between 1998 and 2016, 30 cases of somatic transformation in GCT treated at the Mount Vernon Cancer Centre and St. Bartholomew's Hospital were identified. The median age at diagnosis was 34 years (range=18-56 years). The histological diagnosis at transformation was rhabdomyosarcoma, sarcomatoid yolk sac, sarcoma (non-specified), clear cell carcinoma, adenocarcinoma and primitive neuro ectodermal tumour (PNET). The 5-year survival rate of all patients was 47%, and that of patients with testicular primary (n=26 patients) was 37%. Somatic transformation component in testicular GCTs is generally considered to be an adverse prognostic factor, however, a reasonable 5-year overall survival rate (87.5%) was observed in patients who present with this at first diagnosis.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
The occurrence of somatic transformation in germ cell tumour (GCT) is rare, with increased incidence in teratomatous tumours. The aim of this study was to understand the clinical outcomes of patients with metastatic GCT with somatic transformation.
MATERIALS AND METHODS METHODS
A retrospective study was conducted in two tertiary cancer centres in London. Between 1998 and 2016, 30 cases of somatic transformation in GCT treated at the Mount Vernon Cancer Centre and St. Bartholomew's Hospital were identified. The median age at diagnosis was 34 years (range=18-56 years). The histological diagnosis at transformation was rhabdomyosarcoma, sarcomatoid yolk sac, sarcoma (non-specified), clear cell carcinoma, adenocarcinoma and primitive neuro ectodermal tumour (PNET).
RESULTS RESULTS
The 5-year survival rate of all patients was 47%, and that of patients with testicular primary (n=26 patients) was 37%.
CONCLUSION CONCLUSIONS
Somatic transformation component in testicular GCTs is generally considered to be an adverse prognostic factor, however, a reasonable 5-year overall survival rate (87.5%) was observed in patients who present with this at first diagnosis.

Identifiants

pubmed: 31519595
pii: 39/9/4911
doi: 10.21873/anticanres.13678
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4911-4916

Informations de copyright

Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Anand Sharma (A)

Department of Medical Oncology, Mount Vernon Cancer Centre, Northwood, U.K. anand.sharma3@nhs.net Constantine.alifrangis1@nhs.net.

Constantine Alifrangis (C)

Department of Oncology, St Bartholomew's Hospital, London, U.K. anand.sharma3@nhs.net Constantine.alifrangis1@nhs.net.
Department of Oncology, University College London Hospital, London, U.K.

Marina Milic (M)

Department of Medical Oncology, Mount Vernon Cancer Centre, Northwood, U.K.

Marcia Hall (M)

Department of Medical Oncology, Mount Vernon Cancer Centre, Northwood, U.K.

Nikhil Vasdev (N)

Department of Urology and Surgery, Lister Hospital, East and North Herts NHS Trust, Stevenage, U.K.

Peter Wilson (P)

Department of Oncology, St Bartholomew's Hospital, London, U.K.

Andrew Gogbashian (A)

Department of Radiology, Mount Vernon Cancer Centre, Paul Strickland Scanner Centre, Northwood, U.K.

David Hrouda (D)

Department of Urology, Imperial College Healthcare NHS Trust, Charing Cross Hospital, London, U.K.

Daniel Berney (D)

Department of Histopathology, Barts Cancer Institute, London, U.K.

Jonathan Shamash (J)

Department of Oncology, St Bartholomew's Hospital, London, U.K.

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