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   <subfield code="a">10.1007/s12094-012-0993-x</subfield>
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   <subfield code="a">Panitumumab and irinotecan every 3weeks is an active and convenient regimen for second-line treatment of patients with wild-type K-RAS metastatic colorectal cancer</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[A. Carrato, A. Gómez, P. Escudero, M. Chaves, F. Rivera, E. Marcuello, E. González, C. Grávalos, M. Constenla, J. Manzano, F. Losa, J. Maurel, R. Dueñas, B. Massuti, J. Gallego, J. Aparicio, A. Antón, E. Aranda]</subfield>
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   <subfield code="a">Purpose: To evaluate the efficacy and safety profile of the combination of panitumumab and irinotecan every 3weeks in a phase II trial as second-line treatment in patients with advanced wild-type (WT) K-RAS colorectal cancer (CRC). Methods: Fifty-three patients received 9mg/kg of panitumumab followed by 350mg/m2 of irinotecan every 21days until disease progression, unacceptable toxicity or consent withdrawal. Results: Median age of patients included was 67years. All patients had previously received 5-fluorouracil, 84% oxaliplatin and 8% irinotecan as first-line treatment. Patients received a median of five infusions of panitumumab and irinotecan. On an intention-to-treat analysis, 12 patients (23%) achieved partial responses and 22 patients (41%) achieved disease stabilization. Median progression-free survival and overall survival were 4.5 and 15.1months, respectively. The most frequent treatment-related severe toxicities per patient were diarrhoea (35.8%), followed by skin rash (32.1%), asthenia (18.9%) and neutropenia (13.2%). A significant association between clinical response and incidence and grade of skin toxicity was observed (p=0.0032). Conclusion: This study shows that the administration of panitumumab plus irinotecan every 3weeks is safe, active and feasible as second-line treatment in patients with advanced WT K-RAS CRC.</subfield>
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   <subfield code="a">Federación de Sociedades Españolas de Oncología (FESEO), 2012</subfield>
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   <subfield code="a">Epidermal growth factor receptor (EGFR) inhibitors</subfield>
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   <subfield code="a">Monoclonal antibodies</subfield>
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   <subfield code="D">A.</subfield>
   <subfield code="u">Medical Oncology Department, Ramón y Cajal University Hospital, Ctra. Colmenar Viejo Km. 9,1, 28034, Madrid, Spain</subfield>
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   <subfield code="a">Escudero</subfield>
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   <subfield code="u">Medical Oncology Department, Clínico Lozano Blesa University Hospital, Zaragoza, Spain</subfield>
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   <subfield code="u">Medical Oncology Department, Virgen del Rocío University Hospital, Sevilla, Spain</subfield>
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   <subfield code="u">Medical Oncology Department, Marqués de Valdecilla University Hospital, Santander, Spain</subfield>
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   <subfield code="u">Medical Oncology Department, Santa Creu i Sant Pau Hospital, Barcelona, Spain</subfield>
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   <subfield code="u">Medical Oncology Department, L′Hospitalet General Hospital, Barcelona, Spain</subfield>
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