| Literature DB >> 27588190 |
Thierry Gil1, Spyridon Sideris1, Fouad Aoun2, Roland van Velthoven2, Nicolas Sirtaine3, Marianne Paesmans4, Lieveke Ameye4, Ahmad Awada1, Daniel Devriendt1, Alexandre Peltier2.
Abstract
Long-term prognosis of germ cell tumor (GCT) types is excellent, however, treatment is associated with non-negligible complication rates and a negative impact on quality of life. The present study described treatment results in terms of survival, both short and long-term toxicity, and paternity rates in a cohort of patients treated at Jules Bordet Institute, University ULB of Brussels (Brussels, Belgium). The present study analyzed the data of a cohort of patients with GCT types. Pre-operative patient and tumor characteristics were described. Performance status, pulmonary function tests and renal clearance prior to chemotherapy were noted. Chemotherapeutic regimens and their associated toxicities were analyzed. The duration to event-free, cancer-specific and overall survivals were estimated using Kaplan-Meier curves. A total of 115 patients (median age, 31-years-old) were treated for a GCT at Jules Bordet Institute. At a median follow-up of 6-years, 11 (10%) patients had relapsed and 2 (2%) developed a second malignant neoplasm. At the final follow-up, 97 (89%) and 6 (5.5%) patients exhibited complete and partial remission, respectively. A total of 6% of patients exhibited a progressive disease. In terms of short-term toxicity, 11% of patients presented with febrile neutropenia. The 10-year overall survival rate and relapse-free survival rate were 93.4 and 89.8%, respectively. The paternity rate post-treatment was 27%. Testicular GCT survivors suffered from short- and long-term treatment-associated side effects on both a physical and psychological level. A long-term close follow-up is necessary in order to assist the patient with these treatment-induced complications.Entities:
Keywords: adverse effects; paternity; quality of life; testicular cancer; testicular cancer survivors
Year: 2016 PMID: 27588190 PMCID: PMC4998096 DOI: 10.3892/mco.2016.960
Source DB: PubMed Journal: Mol Clin Oncol ISSN: 2049-9450