The aim of this study was to evaluate the activity and toxicity of capecitabine as third-line treatment in patients with advanced renal cell carcinoma for whom immunotherapy had failed. Twenty-one patients with metastatic clear renal cell carcinoma were enrolled. Capecitabine was administered orally twice daily at a dosage of 2500 mg/m for 14 days, followed by 7 days of rest. The median number of administered cycles was five (1-13). One patient (4.8%) achieved a remission after eight treatment cycles. Stable disease was observed in nine patients (42.8%), whereas 11 progressed (52.4%). The estimated median time to progression was 3.6 months (confidence interval: 1.4 to 5.2). The estimated median overall survival was 7.2 months (confidence interval: 4.6 to 8.8). The regimen was well tolerated and no unexpected toxic effects were observed. Capecitabine as third-line treatment showed a favourable toxicity profile, but exhibited low activity in patients with advanced renal cell carcinoma after failing immunotherapy. © 2007 Lippincott Williams & Wilkins, Inc.
Capecitabine as third-line treatment in patients with metastatic renal cell carcinoma after failing immunotherapy / Petrioli, Roberto; Paolelli, Loretta; Francini, Edoardo; Marsili, Stefania; Pascucci, Alessandra; Sciandivasci, Angela; de Rubertis, Giovanni; Barbanti, Gabriele; Manganelli, Antonio; Salvestrini, Francesco; Francini, Guido. - In: ANTI-CANCER DRUGS. - ISSN 0959-4973. - ELETTRONICO. - 18:(2007), pp. 817-820. [10.1097/cad.0b013e3280a02f17]
Capecitabine as third-line treatment in patients with metastatic renal cell carcinoma after failing immunotherapy
Francini, Edoardo;
2007
Abstract
The aim of this study was to evaluate the activity and toxicity of capecitabine as third-line treatment in patients with advanced renal cell carcinoma for whom immunotherapy had failed. Twenty-one patients with metastatic clear renal cell carcinoma were enrolled. Capecitabine was administered orally twice daily at a dosage of 2500 mg/m for 14 days, followed by 7 days of rest. The median number of administered cycles was five (1-13). One patient (4.8%) achieved a remission after eight treatment cycles. Stable disease was observed in nine patients (42.8%), whereas 11 progressed (52.4%). The estimated median time to progression was 3.6 months (confidence interval: 1.4 to 5.2). The estimated median overall survival was 7.2 months (confidence interval: 4.6 to 8.8). The regimen was well tolerated and no unexpected toxic effects were observed. Capecitabine as third-line treatment showed a favourable toxicity profile, but exhibited low activity in patients with advanced renal cell carcinoma after failing immunotherapy. © 2007 Lippincott Williams & Wilkins, Inc.| File | Dimensione | Formato | |
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