Risk and prognostic significance of metachronous contralateral testicular germ cell tumours

被引:27
作者
Schaapveld, M. [1 ,2 ]
van den Belt-Dusebout, A. W. [1 ]
Gietema, J. A. [3 ]
de Wit, R. [4 ]
Horenblas, S. [5 ]
Witjes, J. A. [6 ]
Hoekstra, H. J. [7 ]
Kiemeney, L. A. L. M. [2 ,8 ]
Louwman, W. J. [9 ]
Ouwens, G. M. [1 ]
Aleman, B. M. P. [10 ]
van Leeuwen, F. E. [1 ]
机构
[1] Netherlands Canc Inst, Dept Psychosocial Res & Epidemiol, NL-1066 CX Amsterdam, Netherlands
[2] Ctr Comprehens Canc, NL-3501 DB Utrecht, Netherlands
[3] Univ Med Ctr Groningen, Dept Med Oncol, NL-9700 RB Groningen, Netherlands
[4] Dr Daniel Den Hoed Canc Ctr, Erasmus Med Ctr, Dept Med Oncol, NL-3008 AE Rotterdam, Netherlands
[5] Netherlands Canc Inst, Dept Urol, NL-1066 CX Amsterdam, Netherlands
[6] Radboud Univ Nijmegen, Med Ctr, Dept Urol, NL-6500 HB Nijmegen, Netherlands
[7] Univ Groningen, Univ Med Ctr Groningen, Dept Surg Oncol, NL-9700 RB Groningen, Netherlands
[8] Radboud Univ Nijmegen, Med Ctr, Dept Urol & Epidemiol, NL-6500 HB Nijmegen, Netherlands
[9] Comprehens Canc Ctr S, NL-5600 AE Eindhoven, Netherlands
[10] Netherlands Canc Inst, Dept Radiotherapy, NL-1066 CX Amsterdam, Netherlands
关键词
contralateral testicular germ cell tumour; chemotherapy; platinum; cumulative incidence; prognosis; CARCINOMA IN-SITU; COMPETING RISKS; CANCER; CHEMOTHERAPY; EXPERIENCE; TESTIS;
D O I
10.1038/bjc.2012.448
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Testicular germ cell tumour (TGCT) patients are at increased risk of developing a contralateral testicular germ cell tumour (CTGCT). It is unclear whether TGCT treatment affects CTGCT risk. METHODS: The risk of developing a metachronous CTGCT (a CTGCT diagnosed >= 6 months after a primary TGCT) and its impact on patient's prognosis was assessed in a nationwide cohort comprising 3749 TGCT patients treated in the Netherlands during 1965-1995. Standardised incidence ratios (SIRs), comparing CTGCT incidence with TGCT incidence in the general population, and cumulative CTGCT incidence were estimated and CTGCT risk factors assessed, accounting for competing risks. RESULTS: Median follow-up was 18.5 years. Seventy-seven metachronous CTGCTs were diagnosed. The SIR for metachronous CTGCTs was 17.6 (95% confidence interval (95% CI) 13.9-22.0). Standardised incidence ratios remained elevated for up to 20 years, while the 20-year cumulative incidence was 2.2% (95% CI 1.8-2.8%). Platinum-based chemotherapy was associated with a lower CTGCT risk among non-seminoma patients (hazard ratio 0.37, 95% CI 0.18-0.72). The CTGCT patients had a 2.3- fold (95% CI 1.3-4.1) increased risk to develop a subsequent non-TGCT cancer and, consequently, a 1.8-fold (95% CI 1.1-2.9) higher risk of death than patients without a CTGCT. CONCLUSION: The TGCT patients remain at increased risk of a CTGCT for up to 20 years. Treatment with platinum-based chemotherapy reduces this risk. British Journal of Cancer (2012) 107, 1637-1643. doi:10.1038/bjc.2012.448 www.bjcancer.com Published online 11 October 2012 (c) 2012 Cancer Research UK
引用
收藏
页码:1637 / 1643
页数:7
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