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Excellent survival in relapsed stage I testicular cancer
BACKGROUND: Two thirds of patients with germ-cell cancer (GCC) present as clinical stage I (CSI). Following orchiectomy, active surveillance (AS) has become their standard management. However, 15–50% of patients eventually relapse with metastatic disease after AS. Relapses need to be detected early...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503206/ https://www.ncbi.nlm.nih.gov/pubmed/37715132 http://dx.doi.org/10.1186/s12885-023-11388-y |
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author | Speicher, Philip Fankhauser, Christian D. Lorch, Anja Ardizzone, Davide Helnwein, Simon Hoch, Dennis Hermanns, Thomas Beyer, Jörg Akhoundova, Dilara |
author_facet | Speicher, Philip Fankhauser, Christian D. Lorch, Anja Ardizzone, Davide Helnwein, Simon Hoch, Dennis Hermanns, Thomas Beyer, Jörg Akhoundova, Dilara |
author_sort | Speicher, Philip |
collection | PubMed |
description | BACKGROUND: Two thirds of patients with germ-cell cancer (GCC) present as clinical stage I (CSI). Following orchiectomy, active surveillance (AS) has become their standard management. However, 15–50% of patients eventually relapse with metastatic disease after AS. Relapses need to be detected early in order to achieve cure and avoid overtreatment. METHODS: We retrospectively analyzed consecutive GCC patients treated at two Swiss academic centers between 2010 and 2020. Patients with stage IS and extragonadal primaries were excluded. We compared disease characteristics and survival outcomes of patients relapsed from initial CSI to patients with de novo metastatic disease. Primary endpoint was the IGCCCG category at the time of relapse. Main secondary endpoints were progression-free survival (PFS) and overall survival (OS). RESULTS: We identified 360 GCC patients with initial CSI and 245 de novo metastatic patients. After a median follow-up of 47 months, 81 of 360 (22.5%) CSI patients relapsed: 41 seminoma (Sem) and 40 non-seminoma (NSem) patients. All Sems relapsed in the IGCCCG good prognosis group. NSem relapsed with good 29/40 (72.5%) and intermediate 11/40 (27.5%) prognostic features; 95.1% of relapses occurred within five years post-orchiectomy. Only 3 relapsed NSem patients died from metastatic disease. Five-year OS for relapsed CSI patients was 100% for Sem and 87% (95% CI: 61–96%) for NSem patients; five-year PFS was 92% (95% CI: 77–97) and 78% (95% CI: 56–90) for Sem and NSem, respectively. When stratified by IGCCCG prognostic groups, good risk relapsed patients had a trend towards better OS and PFS as compared to de novo metastatic patients. CONCLUSIONS: GCC patients who relapse after initial CSI can be detected early by active surveillance and have an excellent survival. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11388-y. |
format | Online Article Text |
id | pubmed-10503206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105032062023-09-16 Excellent survival in relapsed stage I testicular cancer Speicher, Philip Fankhauser, Christian D. Lorch, Anja Ardizzone, Davide Helnwein, Simon Hoch, Dennis Hermanns, Thomas Beyer, Jörg Akhoundova, Dilara BMC Cancer Research BACKGROUND: Two thirds of patients with germ-cell cancer (GCC) present as clinical stage I (CSI). Following orchiectomy, active surveillance (AS) has become their standard management. However, 15–50% of patients eventually relapse with metastatic disease after AS. Relapses need to be detected early in order to achieve cure and avoid overtreatment. METHODS: We retrospectively analyzed consecutive GCC patients treated at two Swiss academic centers between 2010 and 2020. Patients with stage IS and extragonadal primaries were excluded. We compared disease characteristics and survival outcomes of patients relapsed from initial CSI to patients with de novo metastatic disease. Primary endpoint was the IGCCCG category at the time of relapse. Main secondary endpoints were progression-free survival (PFS) and overall survival (OS). RESULTS: We identified 360 GCC patients with initial CSI and 245 de novo metastatic patients. After a median follow-up of 47 months, 81 of 360 (22.5%) CSI patients relapsed: 41 seminoma (Sem) and 40 non-seminoma (NSem) patients. All Sems relapsed in the IGCCCG good prognosis group. NSem relapsed with good 29/40 (72.5%) and intermediate 11/40 (27.5%) prognostic features; 95.1% of relapses occurred within five years post-orchiectomy. Only 3 relapsed NSem patients died from metastatic disease. Five-year OS for relapsed CSI patients was 100% for Sem and 87% (95% CI: 61–96%) for NSem patients; five-year PFS was 92% (95% CI: 77–97) and 78% (95% CI: 56–90) for Sem and NSem, respectively. When stratified by IGCCCG prognostic groups, good risk relapsed patients had a trend towards better OS and PFS as compared to de novo metastatic patients. CONCLUSIONS: GCC patients who relapse after initial CSI can be detected early by active surveillance and have an excellent survival. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11388-y. BioMed Central 2023-09-15 /pmc/articles/PMC10503206/ /pubmed/37715132 http://dx.doi.org/10.1186/s12885-023-11388-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Speicher, Philip Fankhauser, Christian D. Lorch, Anja Ardizzone, Davide Helnwein, Simon Hoch, Dennis Hermanns, Thomas Beyer, Jörg Akhoundova, Dilara Excellent survival in relapsed stage I testicular cancer |
title | Excellent survival in relapsed stage I testicular cancer |
title_full | Excellent survival in relapsed stage I testicular cancer |
title_fullStr | Excellent survival in relapsed stage I testicular cancer |
title_full_unstemmed | Excellent survival in relapsed stage I testicular cancer |
title_short | Excellent survival in relapsed stage I testicular cancer |
title_sort | excellent survival in relapsed stage i testicular cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503206/ https://www.ncbi.nlm.nih.gov/pubmed/37715132 http://dx.doi.org/10.1186/s12885-023-11388-y |
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