Literature DB >> 10444127

The changing distribution of stage in nonseminomatous testicular germ cell tumours, from 1977 to 1996.

D J Sonneveld1, H J Hoekstra, W T Van Der Graaf, W J Sluiter, H Schraffordt Koops, D T Sleijfer.   

Abstract

OBJECTIVE: To determine the changes between 1977 and 1996 in the distribution of stages of testicular cancer (TC). PATIENTS AND METHODS: The stage distribution was assessed, using various classifications, i.e. the Royal Marsden (RM), Indiana, European Organization for Research and Treatment of Cancer (EORTC), International Germ Cell Cancer Collaborative Group (IGCCCG) and the Medical Research Council (MRC), in 517 patients with nonseminomatous testicular germ cell tumours (NSTGCTs) diagnosed at a single institution between 1977 and 1996.
RESULTS: The number of patients in four consecutive 5-year periods (1977-81, 1982-86, 1987-91, 1992-96) was 119, 141, 141, and 116, respectively. Frequency analyses showed a significant increase of RM stage I, in proportion to stage II-IV, in 1982-86 (55%, odds ratio, OR, 2.54), 1987-91 (53%, OR 2.33) and 1992-96 (61%, OR 3.24) compared to the period 1977-81 (33%). A separate analysis of patients with disseminated disease showed a proportionate significant decrease of RM stage II in 1992-96 (29%, OR 0.43) compared with 1977-81 (49%). There was also a relative decrease of good-prognosis patients with disseminated disease in 1992-96 compared with 1977-81, using analyses of the Indiana (from 56% to 33%, OR 0.39) and EORTC classification (from 78% to 56%, OR 0.36). Analyses of the IGCCCG and MRC classification showed a significant decrease of good-prognosis patients in the 1982-86 compared with the first 5-year period (for IGCCCG, from 54% to 35%, OR 0.46, and for MRC, from 43% to 24%, OR 0.42).
CONCLUSION: The stage distribution of NSTGCT over the past two decades has changed. The proportion of stage I patients has increased since the early 1980s, apparently resulting from a shift of low-extent disseminated disease to stage I disease. This finding is relevant in reducing the treatment required in a higher proportion of patients and the subsequent reduction of long-term risk from treatment.

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Year:  1999        PMID: 10444127     DOI: 10.1046/j.1464-410x.1999.00072.x

Source DB:  PubMed          Journal:  BJU Int        ISSN: 1464-4096            Impact factor:   5.588


  7 in total

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Authors:  Binbing Yu; Lan Huang; Ram C Tiwari; Eric J Feuer; Karen A Johnson
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2.  Epidemiological pattern and time trends in testicular germ-cell tumors: a single institution 20-year experience.

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Review 4.  Treatment of stage I testicular germ-cell tumors.

Authors:  Jorge Aparicio; J R Germà
Journal:  Med Oncol       Date:  2006       Impact factor: 3.738

5.  Mortality and incidence of second cancers following treatment for testicular cancer.

Authors:  D Robinson; H Møller; A Horwich
Journal:  Br J Cancer       Date:  2007-01-30       Impact factor: 7.640

6.  Survival from testicular cancer in England and Wales up to 2001.

Authors:  R A Huddart
Journal:  Br J Cancer       Date:  2008-09-23       Impact factor: 7.640

7.  A decision-analytic approach to define poor prognosis patients: a case study for non-seminomatous germ cell cancer patients.

Authors:  Merel R van Dijk; Ewout W Steyerberg; J Dik F Habbema
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  7 in total

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