Age as a Predictor of Treatment Outcome in Metastatic Testicular Germ Cell Tumors.


Journal

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

Informations de publication

Date de publication:
Oct 2019
Historique:
received: 14 08 2019
revised: 30 08 2019
accepted: 03 09 2019
entrez: 2 10 2019
pubmed: 2 10 2019
medline: 9 10 2019
Statut: ppublish

Résumé

To quantify the prognostic impact of age on relapse and mortality in patients with metastatic testicular germ cell tumors (TGCT). Electronical medical records of 1,225 TGCT patients who were treated at a single academic center between 1994 and 2015 were reviewed. Higher age did not predict for worse progression-free survival (PFS) or for higher progression risk. The corresponding 5-year PFS estimates were 85% in patients younger than 40 years and 83% in the elderly population. Although not statistically significant, higher age was numerically associated with worse overall survival (OS) (univariate HR per five years increase in age=1.18, 95%CI=0.99-1.41). This was explained in regression analysis where age predicted for significantly higher risk of treatment-related death (p=0.022). Elderly patients with metastatic TGCT can achieve high cure rates similar to younger patients if they tolerate risk-adapted chemotherapy.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
To quantify the prognostic impact of age on relapse and mortality in patients with metastatic testicular germ cell tumors (TGCT).
PATIENTS AND METHODS METHODS
Electronical medical records of 1,225 TGCT patients who were treated at a single academic center between 1994 and 2015 were reviewed.
RESULTS RESULTS
Higher age did not predict for worse progression-free survival (PFS) or for higher progression risk. The corresponding 5-year PFS estimates were 85% in patients younger than 40 years and 83% in the elderly population. Although not statistically significant, higher age was numerically associated with worse overall survival (OS) (univariate HR per five years increase in age=1.18, 95%CI=0.99-1.41). This was explained in regression analysis where age predicted for significantly higher risk of treatment-related death (p=0.022).
CONCLUSION CONCLUSIONS
Elderly patients with metastatic TGCT can achieve high cure rates similar to younger patients if they tolerate risk-adapted chemotherapy.

Identifiants

pubmed: 31570454
pii: 39/10/5589
doi: 10.21873/anticanres.13753
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5589-5596

Informations de copyright

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

Auteurs

Angelika Terbuch (A)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Florian Posch (F)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Thomas Bauernhofer (T)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Martin Pichler (M)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.
Department of Experimental Therapeutics, The University of Texas, MD Anderson Cancer Center, Houston, TX, U.S.A.

Heidi Peinsith (H)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Joanna Szkandera (J)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Jakob Riedl (J)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Georg C Hutterer (GC)

Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.
Department of Urology, Medical University of Graz, Graz, Austria.

Karl Pummer (K)

Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.
Department of Urology, Medical University of Graz, Graz, Austria.

Richard Partl (R)

Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.
Department of Therapeutic Radiology and Oncology, Medical University of Graz, Graz, Austria.

Karin S Kapp (KS)

Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.
Department of Therapeutic Radiology and Oncology, Medical University of Graz, Graz, Austria.

Herbert Stöger (H)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Michael Stotz (M)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria Michael.stotz@medunigraz.at.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Armin Gerger (A)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.
Research Unit Genetic Epidemiology and Pharmacogenetics, Medical University of Graz, Graz, Austria.

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