An analysis of surveillance for stage I combined teratoma - seminoma of the testis
Author(s) -
R. Thomas,
D.P. Dearnaley,
J. Nicholls,
A. Norman,
Sarah Sampson,
A. Horwich
Publication year - 1996
Publication title -
british journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.833
H-Index - 236
eISSN - 1532-1827
pISSN - 0007-0920
DOI - 10.1038/bjc.1996.315
Subject(s) - seminoma , teratoma , stage (stratigraphy) , medicine , testicular cancer , germ cell , pathology , oncology , cancer , chemotherapy , biology , paleontology , biochemistry , gene
We analysed 973 patients with stage I testicular tumours presenting between 1983 and 1994. The median ages at presentation for non-seminomatous germ cell tumour (teratoma) were 27 years, seminoma 36 years and combined tumour 33 years. These differences were statistically significant (Mann-Whitney P < 0.05), suggesting that combined tumours may have a separate natural history. We, therefore, analysed all stage I patients managed with surveillance (530 in total) post orchidectomy. The actuarial 5 year relapse-free survival and anatomical patterns of relapse were identical for non-seminomatous germ cell tumour (NSGCT) and combined tumour and both were statistically distinct from seminoma (P = 0.01, log-rank test, chi-square test P = 0.001). The association of seminoma within a histologically confirmed NSGCT has no influence on the clinical outcome.
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