Cargando…
A phase II study evaluating the use of concurrent mitomycin C and capecitabine in patients with advanced unresectable pseudomyxoma peritonei
Pseudomyxoma peritonei (PMP) is a rare neoplastic process characterised by progressive intra-abdominal dissemination of mucinous tumour, and generally considered resistant to systemic chemotherapy. A phase II study in patients with advanced unresectable PMP was undertaken to evaluate the combination...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527821/ https://www.ncbi.nlm.nih.gov/pubmed/18682713 http://dx.doi.org/10.1038/sj.bjc.6604522 |
_version_ | 1782158843285864448 |
---|---|
author | Farquharson, A L Pranesh, N Witham, G Swindell, R Taylor, M B Renehan, A G Rout, S Wilson, M S O'Dwyer, S T Saunders, M P |
author_facet | Farquharson, A L Pranesh, N Witham, G Swindell, R Taylor, M B Renehan, A G Rout, S Wilson, M S O'Dwyer, S T Saunders, M P |
author_sort | Farquharson, A L |
collection | PubMed |
description | Pseudomyxoma peritonei (PMP) is a rare neoplastic process characterised by progressive intra-abdominal dissemination of mucinous tumour, and generally considered resistant to systemic chemotherapy. A phase II study in patients with advanced unresectable PMP was undertaken to evaluate the combination of systemic concurrent mitomycin C (7 mg m(−2) i.v. on day 1) and capecitabine (1250 mg m(−2) b.d. on days 1–14) in a 3-weekly cycle (MCap). Response was determined by semiquantitative assessment of disease volume on serial computed tomographic (CT) scans and serum tumour marker (CEA, CA125, CA19-9) changes at 12 weeks. Between 2003 and 2006, 40 patients were recruited through a national centre for the treatment of peritoneal surface tumours. At baseline, 23 patients had progressive disease and 17 had stable disease. Of 39 assessable patients, 15 (38%, 95% confidence intervals (CIs): 25, 54%) benefited from chemotherapy in the form of either reductions in mucinous deposition or stabilisation of progressive pretreatment disease determined on CT scan. Notably, two patients, originally considered unresectable, following MCap and re-staging underwent potentially curative cytoreductive surgery. Grade 3/4 toxicity rates were low (6%, 95% CIs: 4, 9%). Twenty out of 29 assessed patients (69%, 95% CIs: 51, 83%) felt that their Global Health Status improved during chemotherapy. This is the first trial to demonstrate an apparent benefit of systemic chemotherapy in patients with advanced unresectable PMP. |
format | Text |
id | pubmed-2527821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-25278212009-09-11 A phase II study evaluating the use of concurrent mitomycin C and capecitabine in patients with advanced unresectable pseudomyxoma peritonei Farquharson, A L Pranesh, N Witham, G Swindell, R Taylor, M B Renehan, A G Rout, S Wilson, M S O'Dwyer, S T Saunders, M P Br J Cancer Clinical Study Pseudomyxoma peritonei (PMP) is a rare neoplastic process characterised by progressive intra-abdominal dissemination of mucinous tumour, and generally considered resistant to systemic chemotherapy. A phase II study in patients with advanced unresectable PMP was undertaken to evaluate the combination of systemic concurrent mitomycin C (7 mg m(−2) i.v. on day 1) and capecitabine (1250 mg m(−2) b.d. on days 1–14) in a 3-weekly cycle (MCap). Response was determined by semiquantitative assessment of disease volume on serial computed tomographic (CT) scans and serum tumour marker (CEA, CA125, CA19-9) changes at 12 weeks. Between 2003 and 2006, 40 patients were recruited through a national centre for the treatment of peritoneal surface tumours. At baseline, 23 patients had progressive disease and 17 had stable disease. Of 39 assessable patients, 15 (38%, 95% confidence intervals (CIs): 25, 54%) benefited from chemotherapy in the form of either reductions in mucinous deposition or stabilisation of progressive pretreatment disease determined on CT scan. Notably, two patients, originally considered unresectable, following MCap and re-staging underwent potentially curative cytoreductive surgery. Grade 3/4 toxicity rates were low (6%, 95% CIs: 4, 9%). Twenty out of 29 assessed patients (69%, 95% CIs: 51, 83%) felt that their Global Health Status improved during chemotherapy. This is the first trial to demonstrate an apparent benefit of systemic chemotherapy in patients with advanced unresectable PMP. Nature Publishing Group 2008-08-19 2008-08-05 /pmc/articles/PMC2527821/ /pubmed/18682713 http://dx.doi.org/10.1038/sj.bjc.6604522 Text en Copyright © 2008 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 Study Farquharson, A L Pranesh, N Witham, G Swindell, R Taylor, M B Renehan, A G Rout, S Wilson, M S O'Dwyer, S T Saunders, M P A phase II study evaluating the use of concurrent mitomycin C and capecitabine in patients with advanced unresectable pseudomyxoma peritonei |
title | A phase II study evaluating the use of concurrent mitomycin C and capecitabine in patients with advanced unresectable pseudomyxoma peritonei |
title_full | A phase II study evaluating the use of concurrent mitomycin C and capecitabine in patients with advanced unresectable pseudomyxoma peritonei |
title_fullStr | A phase II study evaluating the use of concurrent mitomycin C and capecitabine in patients with advanced unresectable pseudomyxoma peritonei |
title_full_unstemmed | A phase II study evaluating the use of concurrent mitomycin C and capecitabine in patients with advanced unresectable pseudomyxoma peritonei |
title_short | A phase II study evaluating the use of concurrent mitomycin C and capecitabine in patients with advanced unresectable pseudomyxoma peritonei |
title_sort | phase ii study evaluating the use of concurrent mitomycin c and capecitabine in patients with advanced unresectable pseudomyxoma peritonei |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527821/ https://www.ncbi.nlm.nih.gov/pubmed/18682713 http://dx.doi.org/10.1038/sj.bjc.6604522 |
work_keys_str_mv | AT farquharsonal aphaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT praneshn aphaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT withamg aphaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT swindellr aphaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT taylormb aphaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT renehanag aphaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT routs aphaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT wilsonms aphaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT odwyerst aphaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT saundersmp aphaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT farquharsonal phaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT praneshn phaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT withamg phaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT swindellr phaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT taylormb phaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT renehanag phaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT routs phaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT wilsonms phaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT odwyerst phaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei AT saundersmp phaseiistudyevaluatingtheuseofconcurrentmitomycincandcapecitabineinpatientswithadvancedunresectablepseudomyxomaperitonei |