Survival and New Prognosticators in Metastatic Seminoma: Results From the IGCCCG-Update Consortium.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
10 05 2021
Historique:
pubmed: 18 3 2021
medline: 14 10 2021
entrez: 17 3 2021
Statut: ppublish

Résumé

The classification of the International Germ-Cell Cancer Collaborative Group (IGCCCG) has been a major advance in the management of germ-cell tumors, but relies on data of only 660 patients with seminoma treated between 1975 and 1990. We re-evaluated this classification in a database from a large international consortium. Data on 2,451 men with metastatic seminoma treated with cisplatin- and etoposide-based first-line chemotherapy between 1990 and 2013 were collected from 30 institutions or collaborative groups in Australia, Europe, and North America. Clinical trial and registry data were included. Primary end points were progression-free survival (PFS) and overall survival (OS) calculated from day 1 of treatment. Variables at initial presentation were evaluated for their prognostic impact. Results were validated in an independent validation set of 764 additional patients. Compared with the initial IGCCCG classification, in our modern series, 5-year PFS improved from 82% to 89% (95% CI, 87 to 90) and 5-year OS from 86% to 95% (95% CI, 94 to 96) in good prognosis, and from 67% to 79% (95% CI, 70 to 85) and 72% to 88% (95% CI, 80 to 93) in intermediate prognosis patients. Lactate dehydrogenase (LDH) proved to be an additional adverse prognostic factor. Good prognosis patients with LDH above 2.5× upper limit of normal had a 3-year PFS of 80% (95% CI, 75 to 84) and a 3-year OS of 92% (95% CI, 88 to 95) versus 92% (95% CI, 90 to 94) and 97% (95% CI, 96 to 98) in the group with lower LDH. PFS and OS in metastatic seminoma significantly improved in our modern series compared with the original data. The original IGCCCG classification retains its relevance, but can be further refined by adding LDH at a cutoff of 2.5× upper limit of normal as an additional adverse prognostic factor.

Identifiants

pubmed: 33729863
doi: 10.1200/JCO.20.03292
pmc: PMC8099394
doi:

Substances chimiques

L-Lactate Dehydrogenase EC 1.1.1.27

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1553-1562

Subventions

Organisme : Medical Research Council
ID : MC_U122861331
Pays : United Kingdom
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

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Auteurs

Jörg Beyer (J)

Department of Medical Oncology, Inselspital, University Hospital, University of Bern, Bern, Switzerland.

Laurence Collette (L)

European Organisation for Research and Treatment of Cancer, Brussels, Belgium.

Nicolas Sauvé (N)

European Organisation for Research and Treatment of Cancer, Brussels, Belgium.

Gedske Daugaard (G)

Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Darren R Feldman (DR)

Memorial Sloan Kettering Cancer Center, New York, NY.
Weill Medical College of Cornell University, New York, NY.

Torgrim Tandstad (T)

The Cancer Clinic, St Olavs University Hospital and Department of Clinical and Molecular Medicine, The Norwegian University of Science and Technology, Trondheim, Norway.

Alexey Tryakin (A)

N.N. Blokhin Russian Cancer Research Center, Moscow, Russian Federation.
Research Institute of Oncology at Bashkir State Medical University, Ufa, Russian Federation.

Olof Stahl (O)

Department of Oncology, Skåne University Hospital, Lund, Sweden.

Enrique Gonzalez-Billalabeitia (E)

Servicio de Oncologia Medica, Hospital Universitario 12 de Octubre, Madrid, Spain.
Universidad Catolica San Antonio de Murcia, UCAM, Murcia, Spain.

Ugo De Giorgi (U)

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola, Italy and the Italian Germ Cell Cancer Group (IGG), Italy.

Stéphane Culine (S)

Department of Medical Oncology, Hôpital Saint-Louis, AP-HP, Faculté de Paris, Paris, France.

Ronald de Wit (R)

Erasmus MC Cancer Institute, Rotterdam, the Netherlands.

Aaron R Hansen (AR)

Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.

Marko Bebek (M)

Department of Oncology, University Hospital Centre Zagreb, Zagreb, Croatia.

Angelika Terbuch (A)

Division of Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Costantine Albany (C)

Indiana University Melvin and Bren Simon Cancer Center, Indianapolis, IN.

Marcus Hentrich (M)

Department of Hematology and Oncology, Red Cross Hospital, University of Munich, Munich, Germany.

Jourik A Gietema (JA)

University Medical Center Groningen, Groningen, the Netherlands.

Helene Negaard (H)

Department of Oncology, Oslo University Hospital, Oslo, Norway.

Robert A Huddart (RA)

Institute of Cancer Research, Sutton, United Kingdom.

Anja Lorch (A)

Department of Medical Oncology and Hematology, University Hospital Zurich, Zurich, Switzerland.
Department of Urology, University Hospital Dusseldorf, Dusseldorf, Germany.

Fay H Cafferty (FH)

Medical Research Council Clinical Trials Unit at University College London (UCL), London, United Kingdom.

Daniel Y C Heng (DYC)

Tom Baker Cancer Centre, University of Calgary, Calgary, Alberta, Canada.

Christopher J Sweeney (CJ)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.

Eric Winquist (E)

Division of Medical Oncology, Western University and London Health Sciences Centre, London, Ontario, Canada.

Michal Chovanec (M)

2nd Department of Oncology, Faculty of Medicine, Comenius University and National Cancer Institute, Bratislava, Slovakia.

Christian Fankhauser (C)

University of Zurich, Zurich, Switzerland.

Daniel Stark (D)

Leeds Institute of Medical Research, University of Leeds, Leeds, United Kingdom.

Peter Grimison (P)

Australian and New Zealand Urogenital and Prostate Cancer Trials Group, Sydney, Australia.

Andrea Necchi (A)

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy. Current affiliation: Vita-Salute San Raffaele University and IRCCS San Raffaele Hospital and Scientific Institute, Milan, Italy.

Ben Tran (B)

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

Axel Heidenreich (A)

Department of Urology, Uro-Oncology, Robot-Assisted and Specialized Urologic Surgery, University Hospital Cologne, Cologne, Germany.

Jonathan Shamash (J)

St Bartholomew's Hospital, London, United Kingdom.

Cora N Sternberg (CN)

Medical Oncology, San Camillo Forlanini Hospital, Rome, Italy. Current affiliation: Englander Institute for Precision Medicine, Weill Cornell Medicine, New York-Presbyterian, New York, NY.

David J Vaughn (DJ)

University of Pennsylvania, Philadelphia, PA.

Ignacio Duran (I)

Hospital Universitario Marques de Valdecilla and IDIVAL, Santander, Spain.

Carsten Bokemeyer (C)

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

Anna Patrikidou (A)

Department of Oncology, Geneva University Hospital, Geneva, Switzerland. Current affiliation: Sarah Cannon Research Institute and UCL Cancer Institute, London, United Kingdom.

Richard Cathomas (R)

Division of Oncology/Hematology, Cantonal Hospital Graubunden, Chur, Switzerland.

Samson Assele (S)

European Organisation for Research and Treatment of Cancer, Brussels, Belgium.

Silke Gillessen (S)

Oncology Institute of Southern Switzerland (IOSI), Bellinzona, Switzerland.
Universita della Svizzera Italiana, Lugano, Switzerland.
University of Manchester, Manchester, United Kingdom.

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