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Impact of tumour burden on chemotherapy-induced nausea and vomiting.

We investigated how residual tumour burden after cytoreductive surgery was related to the occurrence of acute and delayed nausea and vomiting in 101 ovarian cancer patients receiving their first chemotherapy course. The anti-emetic treatment included ondansetron combined with dexamethasone or placeb...

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Autores principales: Hursti, T. J., Avall-Lundqvist, E., Börjeson, S., Fredrikson, M., Fürst, C. J., Steineck, G., Peterson, C.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2077107/
https://www.ncbi.nlm.nih.gov/pubmed/8855984
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author Hursti, T. J.
Avall-Lundqvist, E.
Börjeson, S.
Fredrikson, M.
Fürst, C. J.
Steineck, G.
Peterson, C.
author_facet Hursti, T. J.
Avall-Lundqvist, E.
Börjeson, S.
Fredrikson, M.
Fürst, C. J.
Steineck, G.
Peterson, C.
author_sort Hursti, T. J.
collection PubMed
description We investigated how residual tumour burden after cytoreductive surgery was related to the occurrence of acute and delayed nausea and vomiting in 101 ovarian cancer patients receiving their first chemotherapy course. The anti-emetic treatment included ondansetron combined with dexamethasone or placebo. After chemotherapy all patients received ondansetron only for 5 days. Two categories of tumour burden (TB) were formed according to the diameter of the greatest residual tumour (< 2 cm = minimal TB and > or = 2 cm = large TB). Self-reports of nausea and vomiting were obtained for 15 days. Other potential predictor variables were assessed and included in multivariate analyses. Patients with large compared with minimal TB had more delayed emesis, especially on days 2-7. They also had more acute nausea. The aggravating effect associated with large residual TB was more evident in patients > or = 55 years. During the second week after the chemotherapy the occurrence of nausea was higher in patients > or = 55 years than in those < 55 years. This was seen primarily in patients with large residual TB. Predictors for no delayed emesis at all were anti-emetic treatment with dexamethasone, minimal tumour burden, low neuroticism and no history of motion sickness. The increased risk of "persistent' delayed nausea and vomiting seen in older patients with large tumour burden may have important clinical implications and warrants further attention.
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spelling pubmed-20771072009-09-10 Impact of tumour burden on chemotherapy-induced nausea and vomiting. Hursti, T. J. Avall-Lundqvist, E. Börjeson, S. Fredrikson, M. Fürst, C. J. Steineck, G. Peterson, C. Br J Cancer Research Article We investigated how residual tumour burden after cytoreductive surgery was related to the occurrence of acute and delayed nausea and vomiting in 101 ovarian cancer patients receiving their first chemotherapy course. The anti-emetic treatment included ondansetron combined with dexamethasone or placebo. After chemotherapy all patients received ondansetron only for 5 days. Two categories of tumour burden (TB) were formed according to the diameter of the greatest residual tumour (< 2 cm = minimal TB and > or = 2 cm = large TB). Self-reports of nausea and vomiting were obtained for 15 days. Other potential predictor variables were assessed and included in multivariate analyses. Patients with large compared with minimal TB had more delayed emesis, especially on days 2-7. They also had more acute nausea. The aggravating effect associated with large residual TB was more evident in patients > or = 55 years. During the second week after the chemotherapy the occurrence of nausea was higher in patients > or = 55 years than in those < 55 years. This was seen primarily in patients with large residual TB. Predictors for no delayed emesis at all were anti-emetic treatment with dexamethasone, minimal tumour burden, low neuroticism and no history of motion sickness. The increased risk of "persistent' delayed nausea and vomiting seen in older patients with large tumour burden may have important clinical implications and warrants further attention. Nature Publishing Group 1996-10 /pmc/articles/PMC2077107/ /pubmed/8855984 Text en 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 Research Article
Hursti, T. J.
Avall-Lundqvist, E.
Börjeson, S.
Fredrikson, M.
Fürst, C. J.
Steineck, G.
Peterson, C.
Impact of tumour burden on chemotherapy-induced nausea and vomiting.
title Impact of tumour burden on chemotherapy-induced nausea and vomiting.
title_full Impact of tumour burden on chemotherapy-induced nausea and vomiting.
title_fullStr Impact of tumour burden on chemotherapy-induced nausea and vomiting.
title_full_unstemmed Impact of tumour burden on chemotherapy-induced nausea and vomiting.
title_short Impact of tumour burden on chemotherapy-induced nausea and vomiting.
title_sort impact of tumour burden on chemotherapy-induced nausea and vomiting.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2077107/
https://www.ncbi.nlm.nih.gov/pubmed/8855984
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