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A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients w...

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Zeitschriftentitel: Cancer Epidemiology, Biomarkers & Prevention
Personen und Körperschaften: Mantovani, Giovanni, Macciò, Antonio, Madeddu, Clelia, Gramignano, Giulia, Lusso, Maria Rita, Serpe, Roberto, Massa, Elena, Astara, Giorgio, Deiana, Laura
In: Cancer Epidemiology, Biomarkers & Prevention, 15, 2006, 5, S. 1030-1034
Format: E-Article
Sprache: Englisch
veröffentlicht:
American Association for Cancer Research (AACR)
Schlagwörter:
author_facet Mantovani, Giovanni
Macciò, Antonio
Madeddu, Clelia
Gramignano, Giulia
Lusso, Maria Rita
Serpe, Roberto
Massa, Elena
Astara, Giorgio
Deiana, Laura
Mantovani, Giovanni
Macciò, Antonio
Madeddu, Clelia
Gramignano, Giulia
Lusso, Maria Rita
Serpe, Roberto
Massa, Elena
Astara, Giorgio
Deiana, Laura
author Mantovani, Giovanni
Macciò, Antonio
Madeddu, Clelia
Gramignano, Giulia
Lusso, Maria Rita
Serpe, Roberto
Massa, Elena
Astara, Giorgio
Deiana, Laura
spellingShingle Mantovani, Giovanni
Macciò, Antonio
Madeddu, Clelia
Gramignano, Giulia
Lusso, Maria Rita
Serpe, Roberto
Massa, Elena
Astara, Giorgio
Deiana, Laura
Cancer Epidemiology, Biomarkers & Prevention
A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress
Oncology
Epidemiology
author_sort mantovani, giovanni
spelling Mantovani, Giovanni Macciò, Antonio Madeddu, Clelia Gramignano, Giulia Lusso, Maria Rita Serpe, Roberto Massa, Elena Astara, Giorgio Deiana, Laura 1055-9965 1538-7755 American Association for Cancer Research (AACR) Oncology Epidemiology http://dx.doi.org/10.1158/1055-9965.epi-05-0538 <jats:title>Abstract</jats:title> <jats:p>Purpose: To test the efficacy and safety of an integrated treatment based on a pharmaconutritional support, antioxidants, and drugs, all given orally, in a population of advanced cancer patients with cancer-related anorexia/cachexia and oxidative stress.</jats:p> <jats:p>Patients and Methods: An open early-phase II study was designed according to the Simon two-stage design. The integrated treatment consisted of diet with high polyphenols content (400 mg), antioxidant treatment (300 mg/d α-lipoic acid + 2.7 g/d carbocysteine lysine salt + 400 mg/d vitamin E + 30,000 IU/d vitamin A + 500 mg/d vitamin C), and pharmaconutritional support enriched with 2 cans per day (n-3)-PUFA (eicosapentaenoic acid and docosahexaenoic acid), 500 mg/d medroxyprogesterone acetate, and 200 mg/d selective cyclooxygenase-2 inhibitor celecoxib. The treatment duration was 4 months. The following variables were evaluated: (a) clinical (Eastern Cooperative Oncology Group performance status); (b) nutritional [lean body mass (LBM), appetite, and resting energy expenditure]; (c) laboratory [proinflammatory cytokines and leptin, reactive oxygen species (ROS) and antioxidant enzymes]; (d) quality of life (European Organization for Research and Treatment of Cancer QLQ-C30, Euro QL-5D, and MFSI-SF).</jats:p> <jats:p>Results: From July 2002 to January 2005, 44 patients were enrolled. Of these, 39 completed the treatment and were assessable. Body weight increased significantly from baseline as did LBM and appetite. There was an important decrease of proinflammatory cytokines interleukin-6 (IL-6) and tumor necrosis factor-α, and a negative relationship worthy of note was only found between LBM and IL-6 changes. As for quality of life evaluation, there was a marked improvement in the European Organization for Research and Treatment of Cancer QLQ-C30, Euro QL-5DVAS, and multidimensional fatigue symptom inventory-short form scores. At the end of the study, 22 of the 39 patients were “responders” or “high responders.” The minimum required was 21; therefore, the treatment was effective and more importantly was shown to be safe.</jats:p> <jats:p>Conclusion: The efficacy and safety of the treatment have been shown by the study; therefore, a randomized phase III study is warranted. (Cancer Epidemiol Biomarkers Prev 2006;15(5):1030–4)</jats:p> A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress Cancer Epidemiology, Biomarkers & Prevention
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title A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress
title_unstemmed A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress
title_full A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress
title_fullStr A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress
title_full_unstemmed A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress
title_short A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress
title_sort a phase ii study with antioxidants, both in the diet and supplemented, pharmaconutritional support, progestagen, and anti-cyclooxygenase-2 showing efficacy and safety in patients with cancer-related anorexia/cachexia and oxidative stress
topic Oncology
Epidemiology
url http://dx.doi.org/10.1158/1055-9965.epi-05-0538
publishDate 2006
physical 1030-1034
description <jats:title>Abstract</jats:title> <jats:p>Purpose: To test the efficacy and safety of an integrated treatment based on a pharmaconutritional support, antioxidants, and drugs, all given orally, in a population of advanced cancer patients with cancer-related anorexia/cachexia and oxidative stress.</jats:p> <jats:p>Patients and Methods: An open early-phase II study was designed according to the Simon two-stage design. The integrated treatment consisted of diet with high polyphenols content (400 mg), antioxidant treatment (300 mg/d α-lipoic acid + 2.7 g/d carbocysteine lysine salt + 400 mg/d vitamin E + 30,000 IU/d vitamin A + 500 mg/d vitamin C), and pharmaconutritional support enriched with 2 cans per day (n-3)-PUFA (eicosapentaenoic acid and docosahexaenoic acid), 500 mg/d medroxyprogesterone acetate, and 200 mg/d selective cyclooxygenase-2 inhibitor celecoxib. The treatment duration was 4 months. The following variables were evaluated: (a) clinical (Eastern Cooperative Oncology Group performance status); (b) nutritional [lean body mass (LBM), appetite, and resting energy expenditure]; (c) laboratory [proinflammatory cytokines and leptin, reactive oxygen species (ROS) and antioxidant enzymes]; (d) quality of life (European Organization for Research and Treatment of Cancer QLQ-C30, Euro QL-5D, and MFSI-SF).</jats:p> <jats:p>Results: From July 2002 to January 2005, 44 patients were enrolled. Of these, 39 completed the treatment and were assessable. Body weight increased significantly from baseline as did LBM and appetite. There was an important decrease of proinflammatory cytokines interleukin-6 (IL-6) and tumor necrosis factor-α, and a negative relationship worthy of note was only found between LBM and IL-6 changes. As for quality of life evaluation, there was a marked improvement in the European Organization for Research and Treatment of Cancer QLQ-C30, Euro QL-5DVAS, and multidimensional fatigue symptom inventory-short form scores. At the end of the study, 22 of the 39 patients were “responders” or “high responders.” The minimum required was 21; therefore, the treatment was effective and more importantly was shown to be safe.</jats:p> <jats:p>Conclusion: The efficacy and safety of the treatment have been shown by the study; therefore, a randomized phase III study is warranted. (Cancer Epidemiol Biomarkers Prev 2006;15(5):1030–4)</jats:p>
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author Mantovani, Giovanni, Macciò, Antonio, Madeddu, Clelia, Gramignano, Giulia, Lusso, Maria Rita, Serpe, Roberto, Massa, Elena, Astara, Giorgio, Deiana, Laura
author_facet Mantovani, Giovanni, Macciò, Antonio, Madeddu, Clelia, Gramignano, Giulia, Lusso, Maria Rita, Serpe, Roberto, Massa, Elena, Astara, Giorgio, Deiana, Laura, Mantovani, Giovanni, Macciò, Antonio, Madeddu, Clelia, Gramignano, Giulia, Lusso, Maria Rita, Serpe, Roberto, Massa, Elena, Astara, Giorgio, Deiana, Laura
author_sort mantovani, giovanni
container_issue 5
container_start_page 1030
container_title Cancer Epidemiology, Biomarkers & Prevention
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description <jats:title>Abstract</jats:title> <jats:p>Purpose: To test the efficacy and safety of an integrated treatment based on a pharmaconutritional support, antioxidants, and drugs, all given orally, in a population of advanced cancer patients with cancer-related anorexia/cachexia and oxidative stress.</jats:p> <jats:p>Patients and Methods: An open early-phase II study was designed according to the Simon two-stage design. The integrated treatment consisted of diet with high polyphenols content (400 mg), antioxidant treatment (300 mg/d α-lipoic acid + 2.7 g/d carbocysteine lysine salt + 400 mg/d vitamin E + 30,000 IU/d vitamin A + 500 mg/d vitamin C), and pharmaconutritional support enriched with 2 cans per day (n-3)-PUFA (eicosapentaenoic acid and docosahexaenoic acid), 500 mg/d medroxyprogesterone acetate, and 200 mg/d selective cyclooxygenase-2 inhibitor celecoxib. The treatment duration was 4 months. The following variables were evaluated: (a) clinical (Eastern Cooperative Oncology Group performance status); (b) nutritional [lean body mass (LBM), appetite, and resting energy expenditure]; (c) laboratory [proinflammatory cytokines and leptin, reactive oxygen species (ROS) and antioxidant enzymes]; (d) quality of life (European Organization for Research and Treatment of Cancer QLQ-C30, Euro QL-5D, and MFSI-SF).</jats:p> <jats:p>Results: From July 2002 to January 2005, 44 patients were enrolled. Of these, 39 completed the treatment and were assessable. Body weight increased significantly from baseline as did LBM and appetite. There was an important decrease of proinflammatory cytokines interleukin-6 (IL-6) and tumor necrosis factor-α, and a negative relationship worthy of note was only found between LBM and IL-6 changes. As for quality of life evaluation, there was a marked improvement in the European Organization for Research and Treatment of Cancer QLQ-C30, Euro QL-5DVAS, and multidimensional fatigue symptom inventory-short form scores. At the end of the study, 22 of the 39 patients were “responders” or “high responders.” The minimum required was 21; therefore, the treatment was effective and more importantly was shown to be safe.</jats:p> <jats:p>Conclusion: The efficacy and safety of the treatment have been shown by the study; therefore, a randomized phase III study is warranted. (Cancer Epidemiol Biomarkers Prev 2006;15(5):1030–4)</jats:p>
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spelling Mantovani, Giovanni Macciò, Antonio Madeddu, Clelia Gramignano, Giulia Lusso, Maria Rita Serpe, Roberto Massa, Elena Astara, Giorgio Deiana, Laura 1055-9965 1538-7755 American Association for Cancer Research (AACR) Oncology Epidemiology http://dx.doi.org/10.1158/1055-9965.epi-05-0538 <jats:title>Abstract</jats:title> <jats:p>Purpose: To test the efficacy and safety of an integrated treatment based on a pharmaconutritional support, antioxidants, and drugs, all given orally, in a population of advanced cancer patients with cancer-related anorexia/cachexia and oxidative stress.</jats:p> <jats:p>Patients and Methods: An open early-phase II study was designed according to the Simon two-stage design. The integrated treatment consisted of diet with high polyphenols content (400 mg), antioxidant treatment (300 mg/d α-lipoic acid + 2.7 g/d carbocysteine lysine salt + 400 mg/d vitamin E + 30,000 IU/d vitamin A + 500 mg/d vitamin C), and pharmaconutritional support enriched with 2 cans per day (n-3)-PUFA (eicosapentaenoic acid and docosahexaenoic acid), 500 mg/d medroxyprogesterone acetate, and 200 mg/d selective cyclooxygenase-2 inhibitor celecoxib. The treatment duration was 4 months. The following variables were evaluated: (a) clinical (Eastern Cooperative Oncology Group performance status); (b) nutritional [lean body mass (LBM), appetite, and resting energy expenditure]; (c) laboratory [proinflammatory cytokines and leptin, reactive oxygen species (ROS) and antioxidant enzymes]; (d) quality of life (European Organization for Research and Treatment of Cancer QLQ-C30, Euro QL-5D, and MFSI-SF).</jats:p> <jats:p>Results: From July 2002 to January 2005, 44 patients were enrolled. Of these, 39 completed the treatment and were assessable. Body weight increased significantly from baseline as did LBM and appetite. There was an important decrease of proinflammatory cytokines interleukin-6 (IL-6) and tumor necrosis factor-α, and a negative relationship worthy of note was only found between LBM and IL-6 changes. As for quality of life evaluation, there was a marked improvement in the European Organization for Research and Treatment of Cancer QLQ-C30, Euro QL-5DVAS, and multidimensional fatigue symptom inventory-short form scores. At the end of the study, 22 of the 39 patients were “responders” or “high responders.” The minimum required was 21; therefore, the treatment was effective and more importantly was shown to be safe.</jats:p> <jats:p>Conclusion: The efficacy and safety of the treatment have been shown by the study; therefore, a randomized phase III study is warranted. (Cancer Epidemiol Biomarkers Prev 2006;15(5):1030–4)</jats:p> A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress Cancer Epidemiology, Biomarkers & Prevention
spellingShingle Mantovani, Giovanni, Macciò, Antonio, Madeddu, Clelia, Gramignano, Giulia, Lusso, Maria Rita, Serpe, Roberto, Massa, Elena, Astara, Giorgio, Deiana, Laura, Cancer Epidemiology, Biomarkers & Prevention, A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress, Oncology, Epidemiology
title A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress
title_full A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress
title_fullStr A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress
title_full_unstemmed A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress
title_short A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress
title_sort a phase ii study with antioxidants, both in the diet and supplemented, pharmaconutritional support, progestagen, and anti-cyclooxygenase-2 showing efficacy and safety in patients with cancer-related anorexia/cachexia and oxidative stress
title_unstemmed A Phase II Study with Antioxidants, Both in the Diet and Supplemented, Pharmaconutritional Support, Progestagen, and Anti-Cyclooxygenase-2 Showing Efficacy and Safety in Patients with Cancer-Related Anorexia/Cachexia and Oxidative Stress
topic Oncology, Epidemiology
url http://dx.doi.org/10.1158/1055-9965.epi-05-0538