Human chorionic gonadotropin-positive seminoma patients: A registry compiled by the global germ cell tumor collaborative group (G3).


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
06 2020
Historique:
received: 25 12 2019
revised: 24 03 2020
accepted: 26 03 2020
pubmed: 4 5 2020
medline: 11 11 2020
entrez: 4 5 2020
Statut: ppublish

Résumé

The prognostic role of human chorionic gonadotropin (hCG) and lactate dehydrogenase (LDH) serum levels in seminoma patients remains uncertain. This observational study evaluates the prognostic impact of tumour marker levels, and other clinicopathological findings, in hCG-positive seminoma patients. Seminoma patients with serum hCG levels above normal at first diagnosis were eligible for recruitment. Statistical analysis, including multivariate regression, was performed to identify risk factors. Primary end-points were overall survival (OS) and recurrence-free survival (RFS). We recruited 1031 hCG-positive patients (stage I: n = 586; stage II + III: n = 427) diagnosed between 1981 and 2018. In metastatic disease, LDH levels ≥3 above upper normal limit (UNL) pre- (n = 109) or post-orchiectomy (n = 73) and patients aged ≥40 years (n = 187) were associated with poor prognosis: 5-year OS rates of 84% (LDH ≥3 UNL pre-orchiectomy) versus 92% (<3 UNL pre-orchiectomy) (hazard ratio [HR]: 3.155, [95% confidence interval {CI}: 1.28-7.75], P = 0.012), 82% (≥3 UNL post-orchiectomy) versus 92% (<3 UNL post-orchiectomy) (HR: 6.877, [95% CI: 1.61-29.34]; P = 0.009) and 86% (≥40 years) versus 91% (<40 years) (HR: 6.870, [95% CI: 1.45-13.37], P = 0.009), respectively. A subset of patients with hCG levels ≥2000 IU/l pre-orchiectomy (n = 17) exhibited a poor prognosis, with 5-year OS rates of 73% (≥2000 IU/l) versus 94% (<2000 IU/l) (HR: 3.936, [95% CI: 1.02-12.61], P = 0.047). Age and LDH levels are significantly associated with poor prognosis in hCG-positive seminoma patients. A small number of patients, with levels of hCG ≥2000 IU/l, may represent a separate prognostic subgroup associated with impaired survival rates.

Sections du résumé

BACKGROUND
The prognostic role of human chorionic gonadotropin (hCG) and lactate dehydrogenase (LDH) serum levels in seminoma patients remains uncertain. This observational study evaluates the prognostic impact of tumour marker levels, and other clinicopathological findings, in hCG-positive seminoma patients.
METHODS
Seminoma patients with serum hCG levels above normal at first diagnosis were eligible for recruitment. Statistical analysis, including multivariate regression, was performed to identify risk factors. Primary end-points were overall survival (OS) and recurrence-free survival (RFS).
RESULTS
We recruited 1031 hCG-positive patients (stage I: n = 586; stage II + III: n = 427) diagnosed between 1981 and 2018. In metastatic disease, LDH levels ≥3 above upper normal limit (UNL) pre- (n = 109) or post-orchiectomy (n = 73) and patients aged ≥40 years (n = 187) were associated with poor prognosis: 5-year OS rates of 84% (LDH ≥3 UNL pre-orchiectomy) versus 92% (<3 UNL pre-orchiectomy) (hazard ratio [HR]: 3.155, [95% confidence interval {CI}: 1.28-7.75], P = 0.012), 82% (≥3 UNL post-orchiectomy) versus 92% (<3 UNL post-orchiectomy) (HR: 6.877, [95% CI: 1.61-29.34]; P = 0.009) and 86% (≥40 years) versus 91% (<40 years) (HR: 6.870, [95% CI: 1.45-13.37], P = 0.009), respectively. A subset of patients with hCG levels ≥2000 IU/l pre-orchiectomy (n = 17) exhibited a poor prognosis, with 5-year OS rates of 73% (≥2000 IU/l) versus 94% (<2000 IU/l) (HR: 3.936, [95% CI: 1.02-12.61], P = 0.047).
CONCLUSIONS
Age and LDH levels are significantly associated with poor prognosis in hCG-positive seminoma patients. A small number of patients, with levels of hCG ≥2000 IU/l, may represent a separate prognostic subgroup associated with impaired survival rates.

Identifiants

pubmed: 32361383
pii: S0959-8049(20)30163-5
doi: 10.1016/j.ejca.2020.03.022
pii:
doi:

Substances chimiques

Chorionic Gonadotropin 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

127-135

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement None declared.

Auteurs

Christoph Seidel (C)

Department of Oncology, Hematology and Bone Marrow Transplantation with Division of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Electronic address: c.seidel@uke.de.

Gedske Daugaard (G)

Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Tim Nestler (T)

Department of Urology, Federal Armed Services Hospital Koblenz, Koblenz, Germany.

Alexey Tryakin (A)

Department of Clinical Pharmacology and Chemotherapy, N. N. Blokhin Russian Cancer Research Center, Moscow, Russian Federation.

Mikhail Fedyanin (M)

Department of Clinical Pharmacology and Chemotherapy, N. N. Blokhin Russian Cancer Research Center, Moscow, Russian Federation.

Christian Fankhauser (C)

Department of Urology, University Hospital Zürich, Zurich, Switzerland.

Thomas Hermanns (T)

Department of Urology, University Hospital Zürich, Zurich, Switzerland.

Jorge Aparicio (J)

Medical Oncology Department, Hospital La Fe, On behalf of the Spanish Germ Cell Cancer Group, Valencia, Spain.

Julia Heinzelbecker (J)

Department of Urology, University Hospital Saarland, Homburg/Saar, Germany.

Pia Paffenholz (P)

Department of Urology, University Hospital Cologne, Cologne, Germany; Department of Urology, Medical University Vienna, Austria.

Axel Heidenreich (A)

Department of Urology, University Hospital Cologne, Cologne, Germany; Department of Urology, Medical University Vienna, Austria.

Ugo De Giorgi (U)

Department of Medical Oncology, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, On behalf of the Italian Germ Cell Cancer Group (IGG), Meldola, Italy.

Richard Cathomas (R)

Department of Oncology/Hematology, Kantonsspital Graubünden, Chur, Switzerland.

Anja Lorch (A)

Department of Oncology and Hematology, University Hospital Zürich, Zurich, Switzerland; Department of Urology, University Hospital Düsseldorf, Düsseldorf, Germany.

Anna Fingerhut (A)

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

Fabian Gayer (F)

Department of Pathology, University Clinic Göttingen, Göttingen, Germany.

Felix Bremmer (F)

Department of Pathology, University Clinic Göttingen, Göttingen, Germany.

Patrizia Giannatempo (P)

Fondazione IRCCS, Istituto Nazionale dei Tumori, Milan, Italy.

Andrea Necchi (A)

Fondazione IRCCS, Istituto Nazionale dei Tumori, Milan, Italy.

Gaetano Aurilio (G)

Medical Division of Urogenital and Head & Neck Cancer, IEO European Institute of Oncology IRCCS, Milan, Italy.

Chiara Casadei (C)

Department of Medical Oncology, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, On behalf of the Italian Germ Cell Cancer Group (IGG), Meldola, Italy.

Ben Tran (B)

Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.

Klaus-Peter Dieckmann (KP)

Department of Urology, Asklepios Klinik Altona, Hodentumorzentrum, Germany.

Margarida Brito (M)

Instituto Português de Oncologia de Lisboa, Lisboa, Portugal.

Christian Ruf (C)

Department of Urology, Federal Armed Services Hospital Koblenz, Koblenz, Germany.

Christoph Oing (C)

Department of Oncology, Hematology and Bone Marrow Transplantation with Division of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Carsten Bokemeyer (C)

Department of Oncology, Hematology and Bone Marrow Transplantation with Division of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

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