Cargando…
Improving the outcome of salvage treatment for non-seminomatous germ cell tumours (NSGCT)
Between 1991–96, 41 patients were treated in this unit for relapsed non-seminomatous germ cell tumours (NSGCT). Twenty-eight patients had raised markers at relapse: 17 required salvage chemotherapy and post-chemotherapy surgery, 11 only chemotherapy. In addition 9 patients received high dose chemoth...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2000
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374648/ https://www.ncbi.nlm.nih.gov/pubmed/10945485 http://dx.doi.org/10.1054/bjoc.2000.1290 |
_version_ | 1782154503300055040 |
---|---|
author | Bono, J S de Paul, J Simpson, A Anthoney, A Kirk, D Underwood, M Graham, J Kaye, S B |
author_facet | Bono, J S de Paul, J Simpson, A Anthoney, A Kirk, D Underwood, M Graham, J Kaye, S B |
author_sort | Bono, J S de |
collection | PubMed |
description | Between 1991–96, 41 patients were treated in this unit for relapsed non-seminomatous germ cell tumours (NSGCT). Twenty-eight patients had raised markers at relapse: 17 required salvage chemotherapy and post-chemotherapy surgery, 11 only chemotherapy. In addition 9 patients received high dose chemotherapy. Overall 16/28 patients (57%) requiring chemotherapy remain alive, 14 (50%) disease free. Of the 17 patients treated with chemotherapy and surgery: 12 remain alive, 10 (59%) with no evaluable disease. Only 4/11 (36%) patients treated with chemotherapy alone remain alive, all in complete remission (CR). For relapse with raised markers, univariate analysis suggests that less than CR to induction therapy, resulting in the presence of residual disease is the most important predictor of poor outcome (P< 0.001). All of the 13 patients relapsing with normal markers remain alive, having been primarily treated surgically. Overall these results indicate an improving outlook for relapsed NSGCT. © 2000 Cancer Research Campaign |
format | Text |
id | pubmed-2374648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23746482009-09-10 Improving the outcome of salvage treatment for non-seminomatous germ cell tumours (NSGCT) Bono, J S de Paul, J Simpson, A Anthoney, A Kirk, D Underwood, M Graham, J Kaye, S B Br J Cancer Regular Article Between 1991–96, 41 patients were treated in this unit for relapsed non-seminomatous germ cell tumours (NSGCT). Twenty-eight patients had raised markers at relapse: 17 required salvage chemotherapy and post-chemotherapy surgery, 11 only chemotherapy. In addition 9 patients received high dose chemotherapy. Overall 16/28 patients (57%) requiring chemotherapy remain alive, 14 (50%) disease free. Of the 17 patients treated with chemotherapy and surgery: 12 remain alive, 10 (59%) with no evaluable disease. Only 4/11 (36%) patients treated with chemotherapy alone remain alive, all in complete remission (CR). For relapse with raised markers, univariate analysis suggests that less than CR to induction therapy, resulting in the presence of residual disease is the most important predictor of poor outcome (P< 0.001). All of the 13 patients relapsing with normal markers remain alive, having been primarily treated surgically. Overall these results indicate an improving outlook for relapsed NSGCT. © 2000 Cancer Research Campaign Nature Publishing Group 2000-07 2000-07-24 /pmc/articles/PMC2374648/ /pubmed/10945485 http://dx.doi.org/10.1054/bjoc.2000.1290 Text en Copyright © 2000 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license 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 license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Regular Article Bono, J S de Paul, J Simpson, A Anthoney, A Kirk, D Underwood, M Graham, J Kaye, S B Improving the outcome of salvage treatment for non-seminomatous germ cell tumours (NSGCT) |
title | Improving the outcome of salvage treatment for non-seminomatous germ cell tumours (NSGCT) |
title_full | Improving the outcome of salvage treatment for non-seminomatous germ cell tumours (NSGCT) |
title_fullStr | Improving the outcome of salvage treatment for non-seminomatous germ cell tumours (NSGCT) |
title_full_unstemmed | Improving the outcome of salvage treatment for non-seminomatous germ cell tumours (NSGCT) |
title_short | Improving the outcome of salvage treatment for non-seminomatous germ cell tumours (NSGCT) |
title_sort | improving the outcome of salvage treatment for non-seminomatous germ cell tumours (nsgct) |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374648/ https://www.ncbi.nlm.nih.gov/pubmed/10945485 http://dx.doi.org/10.1054/bjoc.2000.1290 |
work_keys_str_mv | AT bonojsde improvingtheoutcomeofsalvagetreatmentfornonseminomatousgermcelltumoursnsgct AT paulj improvingtheoutcomeofsalvagetreatmentfornonseminomatousgermcelltumoursnsgct AT simpsona improvingtheoutcomeofsalvagetreatmentfornonseminomatousgermcelltumoursnsgct AT anthoneya improvingtheoutcomeofsalvagetreatmentfornonseminomatousgermcelltumoursnsgct AT kirkd improvingtheoutcomeofsalvagetreatmentfornonseminomatousgermcelltumoursnsgct AT underwoodm improvingtheoutcomeofsalvagetreatmentfornonseminomatousgermcelltumoursnsgct AT grahamj improvingtheoutcomeofsalvagetreatmentfornonseminomatousgermcelltumoursnsgct AT kayesb improvingtheoutcomeofsalvagetreatmentfornonseminomatousgermcelltumoursnsgct |