A phase II trial evaluating capecitabine and irinotecan as second line treatment in patients with oesophago-gastric cancer who have progressed on, or within 3months of platinum-based chemotherapy
Rationale: There is no standard second line therapy for relapsed oesophago-gastric (O-G) cancer. Methods: We recruited 29 eligible patients with relapsed O-G cancer who had progressed during or within 3months of prior chemotherapy to assess the efficacy and toxicity of capecitabine [2,000mg/(m super...
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Veröffentlicht in: | Cancer chemotherapy and pharmacology 2009-07, Vol.64 (3), p.455-462 |
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creator | Leary, Alexandra Assersohn, L Cunningham, D Norman, A R Chong, G Brown, G Ross, P J Costello, C Higgins, L Oates, J |
description | Rationale: There is no standard second line therapy for relapsed oesophago-gastric (O-G) cancer. Methods: We recruited 29 eligible patients with relapsed O-G cancer who had progressed during or within 3months of prior chemotherapy to assess the efficacy and toxicity of capecitabine [2,000mg/(m super(2)day) on days 1-14] and irinotecan (250mg/m super(2)) given every 3weeks. Results: Five patients (17%) demonstrated objective response, while a further seven patients (24%) achieved disease stabilisation. Median progression-free survival and overall survival were 3.1months (95% CI=2.2-4.1months) and 6.5months (95%CI=6-7.1months), respectively. Among symptomatic patients, palliation of tumour-related symptoms included resolution of reflux (5/12 pts), dysphagia (3/9 pts) and weight loss (4/9 pts), improvements in anorexia (4/10 pts), nausea (3/4 pts), vomiting (4/6 pts) and pain (4/16 pts). Grade 3-4 toxicities were diarrhoea (15%), nausea and vomiting (7%), lethargy (31%), neutropenia (31%), anemia (14%) and thrombocytopenia (7%). Conclusions: Capecitabine and irinotecan has anti-tumour activity as second line treatment for relapsed O-G cancer, and provides an important improvement in disease related symptoms. |
doi_str_mv | 10.1007/s00280-008-0893-5 |
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Methods: We recruited 29 eligible patients with relapsed O-G cancer who had progressed during or within 3months of prior chemotherapy to assess the efficacy and toxicity of capecitabine [2,000mg/(m super(2)day) on days 1-14] and irinotecan (250mg/m super(2)) given every 3weeks. Results: Five patients (17%) demonstrated objective response, while a further seven patients (24%) achieved disease stabilisation. Median progression-free survival and overall survival were 3.1months (95% CI=2.2-4.1months) and 6.5months (95%CI=6-7.1months), respectively. Among symptomatic patients, palliation of tumour-related symptoms included resolution of reflux (5/12 pts), dysphagia (3/9 pts) and weight loss (4/9 pts), improvements in anorexia (4/10 pts), nausea (3/4 pts), vomiting (4/6 pts) and pain (4/16 pts). Grade 3-4 toxicities were diarrhoea (15%), nausea and vomiting (7%), lethargy (31%), neutropenia (31%), anemia (14%) and thrombocytopenia (7%). Conclusions: Capecitabine and irinotecan has anti-tumour activity as second line treatment for relapsed O-G cancer, and provides an important improvement in disease related symptoms.</description><identifier>ISSN: 0344-5704</identifier><identifier>EISSN: 1432-0843</identifier><identifier>DOI: 10.1007/s00280-008-0893-5</identifier><language>eng</language><ispartof>Cancer chemotherapy and pharmacology, 2009-07, Vol.64 (3), p.455-462</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Leary, Alexandra</creatorcontrib><creatorcontrib>Assersohn, L</creatorcontrib><creatorcontrib>Cunningham, D</creatorcontrib><creatorcontrib>Norman, A R</creatorcontrib><creatorcontrib>Chong, G</creatorcontrib><creatorcontrib>Brown, G</creatorcontrib><creatorcontrib>Ross, P J</creatorcontrib><creatorcontrib>Costello, C</creatorcontrib><creatorcontrib>Higgins, L</creatorcontrib><creatorcontrib>Oates, J</creatorcontrib><title>A phase II trial evaluating capecitabine and irinotecan as second line treatment in patients with oesophago-gastric cancer who have progressed on, or within 3months of platinum-based chemotherapy</title><title>Cancer chemotherapy and pharmacology</title><description>Rationale: There is no standard second line therapy for relapsed oesophago-gastric (O-G) cancer. Methods: We recruited 29 eligible patients with relapsed O-G cancer who had progressed during or within 3months of prior chemotherapy to assess the efficacy and toxicity of capecitabine [2,000mg/(m super(2)day) on days 1-14] and irinotecan (250mg/m super(2)) given every 3weeks. Results: Five patients (17%) demonstrated objective response, while a further seven patients (24%) achieved disease stabilisation. Median progression-free survival and overall survival were 3.1months (95% CI=2.2-4.1months) and 6.5months (95%CI=6-7.1months), respectively. Among symptomatic patients, palliation of tumour-related symptoms included resolution of reflux (5/12 pts), dysphagia (3/9 pts) and weight loss (4/9 pts), improvements in anorexia (4/10 pts), nausea (3/4 pts), vomiting (4/6 pts) and pain (4/16 pts). Grade 3-4 toxicities were diarrhoea (15%), nausea and vomiting (7%), lethargy (31%), neutropenia (31%), anemia (14%) and thrombocytopenia (7%). 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Conclusions: Capecitabine and irinotecan has anti-tumour activity as second line treatment for relapsed O-G cancer, and provides an important improvement in disease related symptoms.</abstract><doi>10.1007/s00280-008-0893-5</doi></addata></record> |
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title | A phase II trial evaluating capecitabine and irinotecan as second line treatment in patients with oesophago-gastric cancer who have progressed on, or within 3months of platinum-based chemotherapy |
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