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Pretreatment serum markers and lymphocyte response to interleukin-2 therapy

Lymphocytosis is a marker of subcutaneous interleukin (IL)-2 therapy efficacy, whereas baseline elevated inflammatory indices were noticed in IL-2-resistant disease. The aim of this study was to analyse the relationship between pretreatment circulating values of IL-6, neopterin, sIL-2R, ESR and the...

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Autores principales: Fumagalli, L, Lissoni, P, Felice, G Di, Meregalli, S, Valsuani, G, Mengo, S, Rovelli, F
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362330/
https://www.ncbi.nlm.nih.gov/pubmed/10408846
http://dx.doi.org/10.1038/sj.bjc.6690371
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author Fumagalli, L
Lissoni, P
Felice, G Di
Meregalli, S
Valsuani, G
Mengo, S
Rovelli, F
author_facet Fumagalli, L
Lissoni, P
Felice, G Di
Meregalli, S
Valsuani, G
Mengo, S
Rovelli, F
author_sort Fumagalli, L
collection PubMed
description Lymphocytosis is a marker of subcutaneous interleukin (IL)-2 therapy efficacy, whereas baseline elevated inflammatory indices were noticed in IL-2-resistant disease. The aim of this study was to analyse the relationship between pretreatment circulating values of IL-6, neopterin, sIL-2R, ESR and the changes in lymphocyte number in response to IL-2 administration. Twenty metastatic renal cell cancer patients were treated with subcutaneous IL-2 immunotherapy (6 000 000 IU day(−1) for 6 days per week for 4 weeks); tumour response consisted of partial response (PR) in four patients, stable disease (SD) in eight patients and progressive disease (PD) in eight patients. Abnormally high pretreatment values of each marker were found as follows: IL-6 in seven patients, neopterin in nine patients, sIL-2R in 13 patients. In response to IL-2 immunotherapy, a significantly higher mean increase in lymphocyte number and a higher percentage of patients with tumour response or stable disease were observed when pretreatment values of IL-6, neopterin and sIL-2R were within the normal range, in comparison to patients with high values for these markers. The pretreatment excess of these serum inflammatory markers seems to negatively influence both the host and tumour response to IL-2 administration, by preventing the IL-2-induced lymphocytosis and resulting in tumour progression. Further studies are requested to verify if overall survival and quality of life may depend on pretreatment host immune status and/or lymphocyte response after IL-2 administration. © 1999 Cancer Research Campaign
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spelling pubmed-23623302009-09-10 Pretreatment serum markers and lymphocyte response to interleukin-2 therapy Fumagalli, L Lissoni, P Felice, G Di Meregalli, S Valsuani, G Mengo, S Rovelli, F Br J Cancer Regular Article Lymphocytosis is a marker of subcutaneous interleukin (IL)-2 therapy efficacy, whereas baseline elevated inflammatory indices were noticed in IL-2-resistant disease. The aim of this study was to analyse the relationship between pretreatment circulating values of IL-6, neopterin, sIL-2R, ESR and the changes in lymphocyte number in response to IL-2 administration. Twenty metastatic renal cell cancer patients were treated with subcutaneous IL-2 immunotherapy (6 000 000 IU day(−1) for 6 days per week for 4 weeks); tumour response consisted of partial response (PR) in four patients, stable disease (SD) in eight patients and progressive disease (PD) in eight patients. Abnormally high pretreatment values of each marker were found as follows: IL-6 in seven patients, neopterin in nine patients, sIL-2R in 13 patients. In response to IL-2 immunotherapy, a significantly higher mean increase in lymphocyte number and a higher percentage of patients with tumour response or stable disease were observed when pretreatment values of IL-6, neopterin and sIL-2R were within the normal range, in comparison to patients with high values for these markers. The pretreatment excess of these serum inflammatory markers seems to negatively influence both the host and tumour response to IL-2 administration, by preventing the IL-2-induced lymphocytosis and resulting in tumour progression. Further studies are requested to verify if overall survival and quality of life may depend on pretreatment host immune status and/or lymphocyte response after IL-2 administration. © 1999 Cancer Research Campaign Nature Publishing Group 1999-05 1999-05-01 /pmc/articles/PMC2362330/ /pubmed/10408846 http://dx.doi.org/10.1038/sj.bjc.6690371 Text en Copyright © 1999 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
Fumagalli, L
Lissoni, P
Felice, G Di
Meregalli, S
Valsuani, G
Mengo, S
Rovelli, F
Pretreatment serum markers and lymphocyte response to interleukin-2 therapy
title Pretreatment serum markers and lymphocyte response to interleukin-2 therapy
title_full Pretreatment serum markers and lymphocyte response to interleukin-2 therapy
title_fullStr Pretreatment serum markers and lymphocyte response to interleukin-2 therapy
title_full_unstemmed Pretreatment serum markers and lymphocyte response to interleukin-2 therapy
title_short Pretreatment serum markers and lymphocyte response to interleukin-2 therapy
title_sort pretreatment serum markers and lymphocyte response to interleukin-2 therapy
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362330/
https://www.ncbi.nlm.nih.gov/pubmed/10408846
http://dx.doi.org/10.1038/sj.bjc.6690371
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