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The prognostic impact of different tumor marker levels in nonseminomatous germ cell tumor patients with intermediate prognosis: A registry of the International Global Germ Cell Tumor Collaborative Group (G3)

Authors :
Olof Ståhl
Marcus Hentrich
Fadi Taza
Gabriella Cohn-Cedermark
Christoph Oing
Karin Oechsle
Arthur Gerl
Christoph Seidel
Margarida Brito
Gedske Daugaard
Alexey Tryakin
Costantine Albany
Carsten Bokemeyer
Andrea Necchi
Seidel, C
Daugaard, G
Tryakin, A
Necchi, A
Cohn-Cedermark, G
Stahl, O
Hentrich, M
Brito, M
Albany, C
Taza, F
Gerl, A
Oechsle, K
Oing, C
Bokemeyer, C
Source :
Seidel, C, Daugaard, G, Tryakin, A, Necchi, A, Cohn-Cedermark, G, Ståhl, O, Hentrich, M, Brito, M, Albany, C, Taza, F, Gerl, A, Oechsle, K, Oing, C & Bokemeyer, C 2019, ' The prognostic impact of different tumor marker levels in nonseminomatous germ cell tumor patients with intermediate prognosis : A registry of the International Global Germ Cell Tumor Collaborative Group (G3) ', Urologic Oncology: Seminars and Original Investigations, vol. 37, no. 11, pp. 809.e19-809.e25 . https://doi.org/10.1016/j.urolonc.2019.07.020
Publication Year :
2019

Abstract

Background: Germ cell tumor patients with intermediate prognosis (IPGCT) according to the International Germ Cell Cancer Collaborative Group (IGCCCG) classification represent a heterogeneous group with different clinical features. This analysis was performed to investigate the prognostic impact of different tumor marker levels prior to first line chemotherapy within IPGCT. Methods: For this study an international registry for IPGCT was established. Eligibility criteria were intermediate prognosis according to IGCCCG criteria, nonseminomatous histology, male sex, and age ≥ 16 years. Uni- and multivariate analysis were conducted to identify characteristics associated with survival outcomes. Receiver-Operating-Characteristic curve analysis was applied to find cut-off parameters. Five-year overall survival (OS) rate was the primary and 5-year progression-free survival rate the secondary endpoint. Results: This database included 634 IPGCT with a median follow-up of 9.0 years (interquartile range: 14.35). Patients received first line treatment with platinum based chemotherapy, associated with a 5-year OS rate of 87%. The stratification of patients according to AFP levels revealed a correlation between AFP levels and outcome, associated with 5-year OS rates of 88% for AFP levels 2,000 to 6,000 IU/ml (n = 121), and 82% for >6,000 IU/ml (n = 57) prior first course of chemotherapy, respectively (P= 0.013). LDH levels prior fist course of chemotherapy also correlated with outcome associated with 5-year OS rates of 92% for 3 to 4 UNL (n = 34), and 77% for >4 UNL (n = 79), respectively (P= 0.03). Different HCG levels prior chemotherapy were not associated with outcome. In multivariable analysis AFP levels >6,000 IU/ml (P= 0.023; hazard ratio HR 2.263) or >1,982 IU/ml (P= 0.031; HR 1.722), and LDH levels >3 UNL (P< 0.001; HR 2.616) were independent prognosticators for OS. Conclusions: Prognostication according to LDH and AFP levels prior chemotherapy could offer a new approach to stratify patients within the intermediate prognosis cohort. According to our findings, patients with AFP values above 6,000 IU/ml or/and LDH > 3 UNL represent an independent high risk cohort. Our results need to be confirmed in the upcoming IGCCCG reclassification.

Details

Database :
OpenAIRE
Journal :
Seidel, C, Daugaard, G, Tryakin, A, Necchi, A, Cohn-Cedermark, G, Ståhl, O, Hentrich, M, Brito, M, Albany, C, Taza, F, Gerl, A, Oechsle, K, Oing, C & Bokemeyer, C 2019, ' The prognostic impact of different tumor marker levels in nonseminomatous germ cell tumor patients with intermediate prognosis : A registry of the International Global Germ Cell Tumor Collaborative Group (G3) ', Urologic Oncology: Seminars and Original Investigations, vol. 37, no. 11, pp. 809.e19-809.e25 . https://doi.org/10.1016/j.urolonc.2019.07.020
Accession number :
edsair.doi.dedup.....aec63639ec0dd2bfe50caee75f69a5c4
Full Text :
https://doi.org/10.1016/j.urolonc.2019.07.020