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
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
1553-1562Subventions
Organisme : Medical Research Council
ID : MC_U122861331
Pays : United Kingdom
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Références
J Natl Compr Canc Netw. 2019 Dec;17(12):1529-1554
pubmed: 31805523
Ann Oncol. 2018 Aug 1;29(8):1658-1686
pubmed: 30113631
Ann Oncol. 2018 Feb 1;29(2):341-346
pubmed: 29140422
Cancer. 2003 Aug 15;98(4):745-52
pubmed: 12910518
J Clin Oncol. 1994 Jan;12(1):120-6
pubmed: 7505805
J Clin Oncol. 1997 Feb;15(2):594-603
pubmed: 9053482
Eur Urol. 1999 Dec;36(6):601-8
pubmed: 10559615
Eur Urol. 2017 Feb;71(2):290-298
pubmed: 27649970
Control Clin Trials. 1996 Aug;17(4):343-6
pubmed: 8889347
Eur J Cancer. 1997 Aug;33(9):1380-7
pubmed: 9337678
Lancet Oncol. 2014 Dec;15(13):1442-1450
pubmed: 25456363
Ann Oncol. 2018 Feb 1;29(2):347-351
pubmed: 29161363