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A novel biweekly multidrug regimen of gemcitabine, oxaliplatin, 5-fluorouracil (5-FU), and folinic acid (FA) in pretreated patients with advanced colorectal carcinoma
Previous results suggest that GEM affects 5-fluorouracil (5-FU) metabolism and pharmacokinetics in cancer patients, while combined with oxaliplatin, levo-folinic acid, and 5-FU (GOLF regimen), at doses achievable in cancer patients, determines high cytotoxic and proapoptotic antitumour activity in c...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2004
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409742/ https://www.ncbi.nlm.nih.gov/pubmed/15150625 http://dx.doi.org/10.1038/sj.bjc.6601783 |
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author | Correale, P Messinese, S Caraglia, M Marsili, S Piccolomini, A Petrioli, R Ceciarini, F Micheli, L Nencini, C Neri, A Vuolo, G Guarnieri, A Abbruzzese, A Prete, S D Giorgi, G Francini, G |
author_facet | Correale, P Messinese, S Caraglia, M Marsili, S Piccolomini, A Petrioli, R Ceciarini, F Micheli, L Nencini, C Neri, A Vuolo, G Guarnieri, A Abbruzzese, A Prete, S D Giorgi, G Francini, G |
author_sort | Correale, P |
collection | PubMed |
description | Previous results suggest that GEM affects 5-fluorouracil (5-FU) metabolism and pharmacokinetics in cancer patients, while combined with oxaliplatin, levo-folinic acid, and 5-FU (GOLF regimen), at doses achievable in cancer patients, determines high cytotoxic and proapoptotic antitumour activity in colon cancer cells in vitro. On these bases we designed a phase I–II clinical trial testing the GOLF regimen in patients with metastatic colorectal carcinoma, who had received at least a prior line of chemotherapy. In total, 29 patients (20 males and nine females) enrolled in the study received every 2 weeks, gemcitabine (patients #1–3 received 600 mg m(−2); patients # 4–6 received 850 mg m(−2); while patients # 7–29 received 1000 mg m(−2)) on the day 1, levo-folinic acid (100 mg m(−2)) on the days 1 and 2; 5-fluorouracil (400 mg m(−2)) in bolus injection, followed by a 22-h continuous infusion (800 mg m(−2)) on the days 1 and 2, and oxaliplatin (85 mg m(−2)), 6 h after the 5-FU bolus on day 2. The most frequent side effect was grade I–II haematological toxicity. In total, 28 patients were evaluable for response: three achieved a complete response, nine a partial response, 10 had a stable disease, and six progressed. The average time to progression and overall survival of the patients was, respectively, 7.26 and 22 months. Our GOLF combination is well tolerated and seems promising for the treatment of advanced colorectal cancer. |
format | Text |
id | pubmed-2409742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-24097422009-09-10 A novel biweekly multidrug regimen of gemcitabine, oxaliplatin, 5-fluorouracil (5-FU), and folinic acid (FA) in pretreated patients with advanced colorectal carcinoma Correale, P Messinese, S Caraglia, M Marsili, S Piccolomini, A Petrioli, R Ceciarini, F Micheli, L Nencini, C Neri, A Vuolo, G Guarnieri, A Abbruzzese, A Prete, S D Giorgi, G Francini, G Br J Cancer Clinical Previous results suggest that GEM affects 5-fluorouracil (5-FU) metabolism and pharmacokinetics in cancer patients, while combined with oxaliplatin, levo-folinic acid, and 5-FU (GOLF regimen), at doses achievable in cancer patients, determines high cytotoxic and proapoptotic antitumour activity in colon cancer cells in vitro. On these bases we designed a phase I–II clinical trial testing the GOLF regimen in patients with metastatic colorectal carcinoma, who had received at least a prior line of chemotherapy. In total, 29 patients (20 males and nine females) enrolled in the study received every 2 weeks, gemcitabine (patients #1–3 received 600 mg m(−2); patients # 4–6 received 850 mg m(−2); while patients # 7–29 received 1000 mg m(−2)) on the day 1, levo-folinic acid (100 mg m(−2)) on the days 1 and 2; 5-fluorouracil (400 mg m(−2)) in bolus injection, followed by a 22-h continuous infusion (800 mg m(−2)) on the days 1 and 2, and oxaliplatin (85 mg m(−2)), 6 h after the 5-FU bolus on day 2. The most frequent side effect was grade I–II haematological toxicity. In total, 28 patients were evaluable for response: three achieved a complete response, nine a partial response, 10 had a stable disease, and six progressed. The average time to progression and overall survival of the patients was, respectively, 7.26 and 22 months. Our GOLF combination is well tolerated and seems promising for the treatment of advanced colorectal cancer. Nature Publishing Group 2004-05-04 2004-04-13 /pmc/articles/PMC2409742/ /pubmed/15150625 http://dx.doi.org/10.1038/sj.bjc.6601783 Text en Copyright © 2004 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 Correale, P Messinese, S Caraglia, M Marsili, S Piccolomini, A Petrioli, R Ceciarini, F Micheli, L Nencini, C Neri, A Vuolo, G Guarnieri, A Abbruzzese, A Prete, S D Giorgi, G Francini, G A novel biweekly multidrug regimen of gemcitabine, oxaliplatin, 5-fluorouracil (5-FU), and folinic acid (FA) in pretreated patients with advanced colorectal carcinoma |
title | A novel biweekly multidrug regimen of gemcitabine, oxaliplatin, 5-fluorouracil (5-FU), and folinic acid (FA) in pretreated patients with advanced colorectal carcinoma |
title_full | A novel biweekly multidrug regimen of gemcitabine, oxaliplatin, 5-fluorouracil (5-FU), and folinic acid (FA) in pretreated patients with advanced colorectal carcinoma |
title_fullStr | A novel biweekly multidrug regimen of gemcitabine, oxaliplatin, 5-fluorouracil (5-FU), and folinic acid (FA) in pretreated patients with advanced colorectal carcinoma |
title_full_unstemmed | A novel biweekly multidrug regimen of gemcitabine, oxaliplatin, 5-fluorouracil (5-FU), and folinic acid (FA) in pretreated patients with advanced colorectal carcinoma |
title_short | A novel biweekly multidrug regimen of gemcitabine, oxaliplatin, 5-fluorouracil (5-FU), and folinic acid (FA) in pretreated patients with advanced colorectal carcinoma |
title_sort | novel biweekly multidrug regimen of gemcitabine, oxaliplatin, 5-fluorouracil (5-fu), and folinic acid (fa) in pretreated patients with advanced colorectal carcinoma |
topic | Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409742/ https://www.ncbi.nlm.nih.gov/pubmed/15150625 http://dx.doi.org/10.1038/sj.bjc.6601783 |
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