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A phase II trial evaluating capecitabine and irinotecan as second line treatment in patients with oesophago-gastric cancer who have progressed on, or within 3 months of platinum-based chemotherapy

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Abstract

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 3 months of prior chemotherapy to assess the efficacy and toxicity of capecitabine [2,000 mg/(m2 day) on days 1–14] and irinotecan (250 mg/m2) given every 3 weeks.

Results

Five patients (17%) demonstrated objective response, while a further seven patients (24%) achieved disease stabilisation. Median progression-free survival and overall survival were 3.1 months (95% CI = 2.2–4.1 months) and 6.5 months (95%CI = 6–7.1 months), 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.

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Acknowledgment

We are grateful to Roche and Aventis for financial support.

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Correspondence to D. Cunningham.

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Leary, A., Assersohn, L., Cunningham, D. et al. A phase II trial evaluating capecitabine and irinotecan as second line treatment in patients with oesophago-gastric cancer who have progressed on, or within 3 months of platinum-based chemotherapy. Cancer Chemother Pharmacol 64, 455–462 (2009). https://doi.org/10.1007/s00280-008-0893-5

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  • DOI: https://doi.org/10.1007/s00280-008-0893-5

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