Cargando…
Effective combination chemotherapy with paclitaxel and cisplatin with or without human granulocyte colony-stimulating factor and/or erythropoietin in patients with advanced gastric cancer
A phase II trial was performed to determine the antitumour efficacy and tolerance of combined paclitaxel and cisplatin with or without hematopoetic growth factor support in patients with advanced gastric cancer. Forty-five patients with histologically confirmed metastatic gastric cancer were entered...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2002
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375443/ https://www.ncbi.nlm.nih.gov/pubmed/12085176 http://dx.doi.org/10.1038/sj.bjc.6600345 |
_version_ | 1782154656984596480 |
---|---|
author | Kornek, G V Raderer, M Schüll, B Fiebiger, W Gedlicka, C Lenauer, A Depisch, D Schneeweiss, B Lang, F Scheithauer, W |
author_facet | Kornek, G V Raderer, M Schüll, B Fiebiger, W Gedlicka, C Lenauer, A Depisch, D Schneeweiss, B Lang, F Scheithauer, W |
author_sort | Kornek, G V |
collection | PubMed |
description | A phase II trial was performed to determine the antitumour efficacy and tolerance of combined paclitaxel and cisplatin with or without hematopoetic growth factor support in patients with advanced gastric cancer. Forty-five patients with histologically confirmed metastatic gastric cancer were entered in this trial. Treatment consisted of 2-weekly courses of paclitaxel 160 mg per m(2) and cisplatin 60 mg per m(2) both given on day 1. Depending on absolute neutrophil counts on the days of scheduled chemotherapeutic drug administration (1000–2000 per μl), a 5-day course of human granulocyte colony-stimulating factor 5 μg kg(−1) per day was given subcutaneously; in addition, if haemoglobin was <12.0 mg dl(−1), erythropoietin 10 000 IU was administered subcutaneously three times per week. The confirmed overall response rate (intent-to-treat) was 44%, including five complete (11%) and 15 partial remissions (33%). Twelve patients had stable disease (27%), 11 (24%) progressed while on chemotherapy, and two patients were not evaluable. The median time to response was 3 months, the median time to progression 7.0 months, and the median survival time was 11.2 months with 12 patients currently alive. Haematologic toxicity was common, though WHO grade 4 neutropenia occurred in only five patients (11%). Apart from total alopecia in 16 patients (36%), severe non-haematologic adverse reactions included grade 3 peripheral neuropathy in six (13%) and anaphylaxis in two patients. In addition, there was one patient each who experienced grade 3 emesis, diarrhea, and infection, respectively. Our data suggest that the combination of paclitaxel and cisplatin with or without G-CSF and/or erythropoietin has promising therapeutic activity in patients with advanced gastric cancer. British Journal of Cancer (2002) 86, 1858–1863. doi:10.1038/sj.bjc.6600345 www.bjcancer.com © 2002 Cancer Research UK |
format | Text |
id | pubmed-2375443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23754432009-09-10 Effective combination chemotherapy with paclitaxel and cisplatin with or without human granulocyte colony-stimulating factor and/or erythropoietin in patients with advanced gastric cancer Kornek, G V Raderer, M Schüll, B Fiebiger, W Gedlicka, C Lenauer, A Depisch, D Schneeweiss, B Lang, F Scheithauer, W Br J Cancer Clinical A phase II trial was performed to determine the antitumour efficacy and tolerance of combined paclitaxel and cisplatin with or without hematopoetic growth factor support in patients with advanced gastric cancer. Forty-five patients with histologically confirmed metastatic gastric cancer were entered in this trial. Treatment consisted of 2-weekly courses of paclitaxel 160 mg per m(2) and cisplatin 60 mg per m(2) both given on day 1. Depending on absolute neutrophil counts on the days of scheduled chemotherapeutic drug administration (1000–2000 per μl), a 5-day course of human granulocyte colony-stimulating factor 5 μg kg(−1) per day was given subcutaneously; in addition, if haemoglobin was <12.0 mg dl(−1), erythropoietin 10 000 IU was administered subcutaneously three times per week. The confirmed overall response rate (intent-to-treat) was 44%, including five complete (11%) and 15 partial remissions (33%). Twelve patients had stable disease (27%), 11 (24%) progressed while on chemotherapy, and two patients were not evaluable. The median time to response was 3 months, the median time to progression 7.0 months, and the median survival time was 11.2 months with 12 patients currently alive. Haematologic toxicity was common, though WHO grade 4 neutropenia occurred in only five patients (11%). Apart from total alopecia in 16 patients (36%), severe non-haematologic adverse reactions included grade 3 peripheral neuropathy in six (13%) and anaphylaxis in two patients. In addition, there was one patient each who experienced grade 3 emesis, diarrhea, and infection, respectively. Our data suggest that the combination of paclitaxel and cisplatin with or without G-CSF and/or erythropoietin has promising therapeutic activity in patients with advanced gastric cancer. British Journal of Cancer (2002) 86, 1858–1863. doi:10.1038/sj.bjc.6600345 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-06-17 /pmc/articles/PMC2375443/ /pubmed/12085176 http://dx.doi.org/10.1038/sj.bjc.6600345 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 Kornek, G V Raderer, M Schüll, B Fiebiger, W Gedlicka, C Lenauer, A Depisch, D Schneeweiss, B Lang, F Scheithauer, W Effective combination chemotherapy with paclitaxel and cisplatin with or without human granulocyte colony-stimulating factor and/or erythropoietin in patients with advanced gastric cancer |
title | Effective combination chemotherapy with paclitaxel and cisplatin with or without human granulocyte colony-stimulating factor and/or erythropoietin in patients with advanced gastric cancer |
title_full | Effective combination chemotherapy with paclitaxel and cisplatin with or without human granulocyte colony-stimulating factor and/or erythropoietin in patients with advanced gastric cancer |
title_fullStr | Effective combination chemotherapy with paclitaxel and cisplatin with or without human granulocyte colony-stimulating factor and/or erythropoietin in patients with advanced gastric cancer |
title_full_unstemmed | Effective combination chemotherapy with paclitaxel and cisplatin with or without human granulocyte colony-stimulating factor and/or erythropoietin in patients with advanced gastric cancer |
title_short | Effective combination chemotherapy with paclitaxel and cisplatin with or without human granulocyte colony-stimulating factor and/or erythropoietin in patients with advanced gastric cancer |
title_sort | effective combination chemotherapy with paclitaxel and cisplatin with or without human granulocyte colony-stimulating factor and/or erythropoietin in patients with advanced gastric cancer |
topic | Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375443/ https://www.ncbi.nlm.nih.gov/pubmed/12085176 http://dx.doi.org/10.1038/sj.bjc.6600345 |
work_keys_str_mv | AT kornekgv effectivecombinationchemotherapywithpaclitaxelandcisplatinwithorwithouthumangranulocytecolonystimulatingfactorandorerythropoietininpatientswithadvancedgastriccancer AT radererm effectivecombinationchemotherapywithpaclitaxelandcisplatinwithorwithouthumangranulocytecolonystimulatingfactorandorerythropoietininpatientswithadvancedgastriccancer AT schullb effectivecombinationchemotherapywithpaclitaxelandcisplatinwithorwithouthumangranulocytecolonystimulatingfactorandorerythropoietininpatientswithadvancedgastriccancer AT fiebigerw effectivecombinationchemotherapywithpaclitaxelandcisplatinwithorwithouthumangranulocytecolonystimulatingfactorandorerythropoietininpatientswithadvancedgastriccancer AT gedlickac effectivecombinationchemotherapywithpaclitaxelandcisplatinwithorwithouthumangranulocytecolonystimulatingfactorandorerythropoietininpatientswithadvancedgastriccancer AT lenauera effectivecombinationchemotherapywithpaclitaxelandcisplatinwithorwithouthumangranulocytecolonystimulatingfactorandorerythropoietininpatientswithadvancedgastriccancer AT depischd effectivecombinationchemotherapywithpaclitaxelandcisplatinwithorwithouthumangranulocytecolonystimulatingfactorandorerythropoietininpatientswithadvancedgastriccancer AT schneeweissb effectivecombinationchemotherapywithpaclitaxelandcisplatinwithorwithouthumangranulocytecolonystimulatingfactorandorerythropoietininpatientswithadvancedgastriccancer AT langf effectivecombinationchemotherapywithpaclitaxelandcisplatinwithorwithouthumangranulocytecolonystimulatingfactorandorerythropoietininpatientswithadvancedgastriccancer AT scheithauerw effectivecombinationchemotherapywithpaclitaxelandcisplatinwithorwithouthumangranulocytecolonystimulatingfactorandorerythropoietininpatientswithadvancedgastriccancer |