Surveillance for stage I nonseminoma testicular cancer: outcomes and long-term follow-up in a population-based cohort
- PMID: 25267754
- DOI: 10.1200/JCO.2013.53.5831
Surveillance for stage I nonseminoma testicular cancer: outcomes and long-term follow-up in a population-based cohort
Abstract
Purpose: To describe treatment results in a large cohort with stage I nonseminoma germ cell cancer (NSGCC) treated in a surveillance program.
Patients and methods: From January 1, 1984, to December 31, 2007, 1,226 patients with stage I NSGCC, including high-risk patients with vascular invasion, were observed in a surveillance program.
Results: The relapse rate after orchiectomy alone was 30.6% at 5 years. Presence of vascular invasion together with embryonal carcinoma and rete testis invasion in the testicular primary identified a group with a relapse risk of 50%. Without risk factors, the relapse risk was 12%. Eighty percent of relapses were diagnosed within the first year after orchiectomy. The median time to relapse was 5 months (range, 1 to 308 months). Early relapses were mainly detected by increase in tumor markers, and late relapses were detected by computed tomography scans. Relapses after 5 years were seen in 0.5% of the whole cohort or in 1.6% of relapsing patients. The majority of relapses (94.4%) belonged to the good prognostic group according to the International Germ Cell Cancer Collaborative Group classification. The disease-specific survival at 15 years was 99.1%.
Conclusion: A surveillance policy for patients with stage I NSGCC is a safe approach associated with an excellent cure rate and an overall low treatment burden despite a high relapse rate in a small group of patients. We recommend surveillance for patients with stage I NSGCC with immediate systemic treatment at relapse. Clearly defined risk factors for relapse are presented if an option of risk-adapted treatment is preferred.
© 2014 by American Society of Clinical Oncology.
Comment in
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Optimal management of clinical stage I nonseminoma: new data for patients to consider.J Clin Oncol. 2014 Dec 1;32(34):3792-3. doi: 10.1200/JCO.2014.56.5747. Epub 2014 Sep 29. J Clin Oncol. 2014. PMID: 25267744 No abstract available.
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Surveillance for Stage I Nonseminoma Testicular Cancer: Outcomes and Long-Term Follow-Up in a Population-Based Cohort.J Clin Oncol. 2015 Jul 10;33(20):2322. doi: 10.1200/JCO.2015.60.8950. Epub 2015 Jun 1. J Clin Oncol. 2015. PMID: 26033804 No abstract available.
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Management of Clinical Stage I Testicular Cancer: How Should We Define Success?J Clin Oncol. 2015 Jul 10;33(20):2321-2. doi: 10.1200/JCO.2015.60.8885. Epub 2015 Jun 1. J Clin Oncol. 2015. PMID: 26033805 No abstract available.
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Reply to G. Daugaard et al, K. Lu, and L.C. Pagliaro et al.J Clin Oncol. 2015 Jul 10;33(20):2325-6. doi: 10.1200/JCO.2015.60.9289. Epub 2015 Jun 1. J Clin Oncol. 2015. PMID: 26033806 No abstract available.
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Recommendations Regarding Computed Tomography Imaging in Follow-Up for Stage I Nonseminoma Testicular Cancer Remain a Challenge.J Clin Oncol. 2015 Jul 10;33(20):2323. doi: 10.1200/JCO.2014.60.6681. Epub 2015 Jun 1. J Clin Oncol. 2015. PMID: 26033807 No abstract available.
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Reply to C. Rusner et al, L.C. Pagliaro et al, and K. Lu.J Clin Oncol. 2015 Jul 10;33(20):2326-7. doi: 10.1200/JCO.2015.60.9313. Epub 2015 Jun 1. J Clin Oncol. 2015. PMID: 26033816 No abstract available.
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