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                  <mods:namePart>Pérez-Ruiz, Elisabeth</mods:namePart>
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                  <mods:namePart>Velasco, Guillermo de</mods:namePart>
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                  <mods:namePart>Quero-Blanco, Cristina</mods:namePart>
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                  <mods:namePart>Alba-Conejo, Emilio</mods:namePart>
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               <mods:identifier type="citation">Sánchez-Muñoz A, Mendiola C, Pérez-Ruiz E, Rodríguez-Sánchez CA, Jurado JM, Alonso-Carrión L, Ghanem I, de Velasco G, Quero-Blanco C, Alba E. Bevacizumab plus low-dose metronomic oral cyclophosphamide in heavily pretreated patients with recurrent ovarian cancer. Oncology. 2010;79(1-2):98-104. doi: 10.1159/000320602. Epub 2010 Nov 15. PMID: 21079407.</mods:identifier>
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               <mods:abstract>Aim: To retrospectively assess the efficacy and safety of bevacizumab plus low-dose metronomic oral cyclophosphamide&#xd;
in heavily pretreated patients with recurrent ovarian cancer. Patients and Methods: Patients with recurrent ovarian&#xd;
cancer and prior treatment with platinum- and taxanebased chemotherapy were included. Treatment consisted of&#xd;
bevacizumab 10 mg/kg intravenously every 2 weeks plus oral cyclophosphamide 50 mg daily until disease progression&#xd;
or unacceptable toxicity. Response rates (RR) were determined according to RECIST criteria and by monitoring the&#xd;
CA 125 serum tumor marker according to Rustin’s criteria.The endpoints were progression-free survival (PFS), RR, overall&#xd;
survival (OS), and safety. Results: Thirty-eight patients were treated; 79% were platinum resistant and 21% were&#xd;
platinum sensitive. The median number of previous treatments was 4 (range 1–8). Seventy-nine percent of patients&#xd;
had received more than 2 previous lines of treatment. Eightyone percent of patients had received gemcitabine, 76% liposomal&#xd;
doxorubicin, and 50% topotecan. A median of 8 (range 1–70) cycles of bevacizumab were administered. The overall&#xd;
RR was a complete response (CR) in 3 patients (8.1%), a partial response (PR) in 12 (32.4%), and stable disease (SD) 6 6&#xd;
months in 3 (8.1%). The median PFS and OS were 4.5 and 10.7 months, respectively. Thirty-nine percent of patients were&#xd;
progression free for at least 6 months. In an exploratory analysis there was a significant relation of prior platinum response&#xd;
and performance status with the risk of progression.Grade 3–4 toxicities included anemia (1), hypertension (2),&#xd;
hematuria (1), arterial thrombosis in the leg (1), dyspnea (1), and intestinal fistulae (1). There were no cases of gastrointestinal&#xd;
perforation (GIP) or treatment-related deaths. Conclusion: The combination of bevacizumab and metronomic cyclophosphamide&#xd;
was active and well-tolerated in heavily pretreated patients with recurrent ovarian cancer.</mods:abstract>
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               <mods:accessCondition type="useAndReproduction">Attribution-NonCommercial-NoDerivatives 4.0 Internacional</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Ovarios - Cáncer - Tratamiento</mods:topic>
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                  <mods:title>Bevacizumab plus low-dose metronomic oral cyclophosphamide in heavily pretreated patients with recurrent ovarian cancer</mods:title>
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