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Oxaliplatin plus raltitrexed and leucovorin-modulated 5-fluorouracil i.v. bolus: a salvage regimen for colorectal cancer patients

The aim of the present study was to define the activity and tolerability of a triplet regimen including oxaliplatin 130 mg m(−2) (2 h i.v. infusion) and raltitrexed 3.0 mg m(−2) (15 min i.v. infusion) given on day 1, followed by levo-folinic acid 250 mg m(−2) (2 h i.v. infusion) and 5-fluorouracil 1...

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Autores principales: Comella, P, Casaretti, R, Crucitta, E, De Vita, F, Palmeri, S, Avallone, A, Orditura, M, De Lucia, L, Del Prete, S, Catalano, G, Lorusso, V, Comella, G
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375419/
https://www.ncbi.nlm.nih.gov/pubmed/12085178
http://dx.doi.org/10.1038/sj.bjc.6600414
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author Comella, P
Casaretti, R
Crucitta, E
De Vita, F
Palmeri, S
Avallone, A
Orditura, M
De Lucia, L
Del Prete, S
Catalano, G
Lorusso, V
Comella, G
author_facet Comella, P
Casaretti, R
Crucitta, E
De Vita, F
Palmeri, S
Avallone, A
Orditura, M
De Lucia, L
Del Prete, S
Catalano, G
Lorusso, V
Comella, G
author_sort Comella, P
collection PubMed
description The aim of the present study was to define the activity and tolerability of a triplet regimen including oxaliplatin 130 mg m(−2) (2 h i.v. infusion) and raltitrexed 3.0 mg m(−2) (15 min i.v. infusion) given on day 1, followed by levo-folinic acid 250 mg m(−2) (2 h i.v. infusion) and 5-fluorouracil 1050 mg m(−2) i.v. bolus on day 2, every 2 weeks, in pretreated colorectal cancer patients. From April 1999 to December 2000, 50 patients were enrolled: 26 were males and 24 females, their median age was 63 (range, 43–79) years; ECOG performance status was 0 in 26 patients, ⩾1 in 24 patients; 26 patients had received previous adjuvant chemotherapy, 40 patients had been exposed to one or two lines of palliative chemotherapy (including irinotecan in 31 cases); 18 patients were considered chemo-refractory. A total of 288 cycles were administered, with a median number of 6 (range 1–12) courses per patient. A complete response was obtained in three patients, and a partial response in nine patients, giving a major response rate of 24% (95% confidence interval, 13–38%), while 15 further patients showed a stable disease, for an overall control of tumour growth in 60% of patients. Three complete responses and three partial responses were obtained in patients pretreated with irinotecan (response rate, 19%); among refractory patients, three achieved partial responses (response rate, 13%). After a median follow-up of 18 (range, 10–30) months, 40 patients showed a progression of disease: the growth modulation index ranged between 0.2 and 2.5: it was ⩾1.33 (showing a significant delay of tumour growth) in 16 (40%) patients. Actuarial median progression-free survival time was 7.6 months, and median survival time was 13.6 months: estimated probability of survival was 55% at 1 year. Main severe toxicity was neutropenia: World Health Organisation grade 4 affected 32% of patients; non-haematological toxicity was mild: World Health Organisation grade 3 diarrhoea was complained of by 8%, and grade 3 stomatitis by 4% of patients; neurotoxicity (according to Lévi scale) was scored as grade 3 in 8% of patients. In conclusion, this regimen was manageable and active as salvage treatment of advanced colorectal cancer patients; it showed incomplete cross-resistance with irinotecan-based treatments, and proved to delay the progression of disease in a relevant proportion of treated patients. British Journal of Cancer (2002) 86, 1871–1875. doi:10.1038/sj.bjc.6600414 www.bjcancer.com © 2002 Cancer Research UK
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spelling pubmed-23754192009-09-10 Oxaliplatin plus raltitrexed and leucovorin-modulated 5-fluorouracil i.v. bolus: a salvage regimen for colorectal cancer patients Comella, P Casaretti, R Crucitta, E De Vita, F Palmeri, S Avallone, A Orditura, M De Lucia, L Del Prete, S Catalano, G Lorusso, V Comella, G Br J Cancer Clinical The aim of the present study was to define the activity and tolerability of a triplet regimen including oxaliplatin 130 mg m(−2) (2 h i.v. infusion) and raltitrexed 3.0 mg m(−2) (15 min i.v. infusion) given on day 1, followed by levo-folinic acid 250 mg m(−2) (2 h i.v. infusion) and 5-fluorouracil 1050 mg m(−2) i.v. bolus on day 2, every 2 weeks, in pretreated colorectal cancer patients. From April 1999 to December 2000, 50 patients were enrolled: 26 were males and 24 females, their median age was 63 (range, 43–79) years; ECOG performance status was 0 in 26 patients, ⩾1 in 24 patients; 26 patients had received previous adjuvant chemotherapy, 40 patients had been exposed to one or two lines of palliative chemotherapy (including irinotecan in 31 cases); 18 patients were considered chemo-refractory. A total of 288 cycles were administered, with a median number of 6 (range 1–12) courses per patient. A complete response was obtained in three patients, and a partial response in nine patients, giving a major response rate of 24% (95% confidence interval, 13–38%), while 15 further patients showed a stable disease, for an overall control of tumour growth in 60% of patients. Three complete responses and three partial responses were obtained in patients pretreated with irinotecan (response rate, 19%); among refractory patients, three achieved partial responses (response rate, 13%). After a median follow-up of 18 (range, 10–30) months, 40 patients showed a progression of disease: the growth modulation index ranged between 0.2 and 2.5: it was ⩾1.33 (showing a significant delay of tumour growth) in 16 (40%) patients. Actuarial median progression-free survival time was 7.6 months, and median survival time was 13.6 months: estimated probability of survival was 55% at 1 year. Main severe toxicity was neutropenia: World Health Organisation grade 4 affected 32% of patients; non-haematological toxicity was mild: World Health Organisation grade 3 diarrhoea was complained of by 8%, and grade 3 stomatitis by 4% of patients; neurotoxicity (according to Lévi scale) was scored as grade 3 in 8% of patients. In conclusion, this regimen was manageable and active as salvage treatment of advanced colorectal cancer patients; it showed incomplete cross-resistance with irinotecan-based treatments, and proved to delay the progression of disease in a relevant proportion of treated patients. British Journal of Cancer (2002) 86, 1871–1875. doi:10.1038/sj.bjc.6600414 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-06-17 /pmc/articles/PMC2375419/ /pubmed/12085178 http://dx.doi.org/10.1038/sj.bjc.6600414 Text en Copyright © 2002 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
Comella, P
Casaretti, R
Crucitta, E
De Vita, F
Palmeri, S
Avallone, A
Orditura, M
De Lucia, L
Del Prete, S
Catalano, G
Lorusso, V
Comella, G
Oxaliplatin plus raltitrexed and leucovorin-modulated 5-fluorouracil i.v. bolus: a salvage regimen for colorectal cancer patients
title Oxaliplatin plus raltitrexed and leucovorin-modulated 5-fluorouracil i.v. bolus: a salvage regimen for colorectal cancer patients
title_full Oxaliplatin plus raltitrexed and leucovorin-modulated 5-fluorouracil i.v. bolus: a salvage regimen for colorectal cancer patients
title_fullStr Oxaliplatin plus raltitrexed and leucovorin-modulated 5-fluorouracil i.v. bolus: a salvage regimen for colorectal cancer patients
title_full_unstemmed Oxaliplatin plus raltitrexed and leucovorin-modulated 5-fluorouracil i.v. bolus: a salvage regimen for colorectal cancer patients
title_short Oxaliplatin plus raltitrexed and leucovorin-modulated 5-fluorouracil i.v. bolus: a salvage regimen for colorectal cancer patients
title_sort oxaliplatin plus raltitrexed and leucovorin-modulated 5-fluorouracil i.v. bolus: a salvage regimen for colorectal cancer patients
topic Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375419/
https://www.ncbi.nlm.nih.gov/pubmed/12085178
http://dx.doi.org/10.1038/sj.bjc.6600414
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