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A medical nutriment has supportive value in the treatment of colorectal cancer
MSC (Avemar) is a medical nutriment of which preclinical and observational clinical studies suggested an antimetastatic activity with no toxicity. This open-label cohort trial has compared anticancer treatments plus MSC (9 g once daily) vs anticancer treatments alone in colorectal patients, enrolled...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394381/ https://www.ncbi.nlm.nih.gov/pubmed/12888813 http://dx.doi.org/10.1038/sj.bjc.6601153 |
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author | Jakab, F Shoenfeld, Y Balogh, Á Nichelatti, M Hoffmann, A Kahán, Zs Lapis, K Mayer, Á Sápy, P Szentpétery, F Telekes, A Thurzó, L Vágvölgyi, A Hidvégi, M |
author_facet | Jakab, F Shoenfeld, Y Balogh, Á Nichelatti, M Hoffmann, A Kahán, Zs Lapis, K Mayer, Á Sápy, P Szentpétery, F Telekes, A Thurzó, L Vágvölgyi, A Hidvégi, M |
author_sort | Jakab, F |
collection | PubMed |
description | MSC (Avemar) is a medical nutriment of which preclinical and observational clinical studies suggested an antimetastatic activity with no toxicity. This open-label cohort trial has compared anticancer treatments plus MSC (9 g once daily) vs anticancer treatments alone in colorectal patients, enrolled from three oncosurgical centres; cohort allocation was on the basis of patients' choice. Sixty-six colorectal cancer patients received MSC supplement for more than 6 months and 104 patients served as controls (anticancer therapies alone): no statistical difference was noted in the time from diagnosis to the last visit between the two groups. End-point analysis revealed that progression-related events were significantly less frequent in the MSC group (new recurrences: 3.0 vs 17.3%, P<0.01; new metastases: 7.6 vs 23.1%, P<0.01; deaths: 12.1 vs 31.7%, P<0.01). Survival analysis showed significant improvements in the MSC group regarding progression-free (P=0.0184) and overall survivals (P=0.0278) probabilities. Survival predictors in Cox's proportional hazards were UICC stage and MSC treatment. Continuous supplementation of anticancer therapies with MSC for more than 6 months is beneficial to patients with colorectal cancer in terms of overall and progression-free survival. |
format | Text |
id | pubmed-2394381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23943812009-09-10 A medical nutriment has supportive value in the treatment of colorectal cancer Jakab, F Shoenfeld, Y Balogh, Á Nichelatti, M Hoffmann, A Kahán, Zs Lapis, K Mayer, Á Sápy, P Szentpétery, F Telekes, A Thurzó, L Vágvölgyi, A Hidvégi, M Br J Cancer Clinical MSC (Avemar) is a medical nutriment of which preclinical and observational clinical studies suggested an antimetastatic activity with no toxicity. This open-label cohort trial has compared anticancer treatments plus MSC (9 g once daily) vs anticancer treatments alone in colorectal patients, enrolled from three oncosurgical centres; cohort allocation was on the basis of patients' choice. Sixty-six colorectal cancer patients received MSC supplement for more than 6 months and 104 patients served as controls (anticancer therapies alone): no statistical difference was noted in the time from diagnosis to the last visit between the two groups. End-point analysis revealed that progression-related events were significantly less frequent in the MSC group (new recurrences: 3.0 vs 17.3%, P<0.01; new metastases: 7.6 vs 23.1%, P<0.01; deaths: 12.1 vs 31.7%, P<0.01). Survival analysis showed significant improvements in the MSC group regarding progression-free (P=0.0184) and overall survivals (P=0.0278) probabilities. Survival predictors in Cox's proportional hazards were UICC stage and MSC treatment. Continuous supplementation of anticancer therapies with MSC for more than 6 months is beneficial to patients with colorectal cancer in terms of overall and progression-free survival. Nature Publishing Group 2003-08-04 2003-07-29 /pmc/articles/PMC2394381/ /pubmed/12888813 http://dx.doi.org/10.1038/sj.bjc.6601153 Text en Copyright © 2003 Cancer Research UK 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 | Clinical Jakab, F Shoenfeld, Y Balogh, Á Nichelatti, M Hoffmann, A Kahán, Zs Lapis, K Mayer, Á Sápy, P Szentpétery, F Telekes, A Thurzó, L Vágvölgyi, A Hidvégi, M A medical nutriment has supportive value in the treatment of colorectal cancer |
title | A medical nutriment has supportive value in the treatment of colorectal cancer |
title_full | A medical nutriment has supportive value in the treatment of colorectal cancer |
title_fullStr | A medical nutriment has supportive value in the treatment of colorectal cancer |
title_full_unstemmed | A medical nutriment has supportive value in the treatment of colorectal cancer |
title_short | A medical nutriment has supportive value in the treatment of colorectal cancer |
title_sort | medical nutriment has supportive value in the treatment of colorectal cancer |
topic | Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394381/ https://www.ncbi.nlm.nih.gov/pubmed/12888813 http://dx.doi.org/10.1038/sj.bjc.6601153 |
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