Bevacizumab in Clinical Practice: Prescribing Appropriateness Relative to National Indications and Safety

被引:29
作者
Bonifazi, Martina [1 ,2 ]
Rossi, Marta [1 ,3 ]
Moja, Lorenzo [1 ,4 ]
Scigliano, Vincenzo Davide [1 ]
Franchi, Matteo [1 ]
La Vecchia, Carlo [1 ,3 ]
Zocchetti, Carlo [5 ,6 ]
Negri, Eva [1 ]
机构
[1] Ist Ric Farmacol Mario Negri, Dept Epidemiol, I-20156 Milan, Italy
[2] Univ Politecn Marche, Ist Clin Med, Ancona, Italy
[3] Univ Milan, Dipartimento Med Lavoro, Milan, Italy
[4] Univ Milan, Dipartimento Sanita Pubbl Microbol Virol, Milan, Italy
[5] Direz Gen Sanita Reg Lombardia, Osservatorio Epidemiol, Milan, Italy
[6] Unita Operat Governo, Serv Sanit Terr & Polit Appropriatezza & Controll, Milan, Italy
关键词
Appropriateness; Bevacizumab; Metastatic colorectal cancer; Safety; Survival; METASTATIC COLORECTAL-CANCER; LABEL DRUG-USE; OFF-LABEL; MACULAR DEGENERATION; HEALTH-CARE; PHASE-II; LEUCOVORIN; FLUOROURACIL; RANIBIZUMAB; THERAPY;
D O I
10.1634/theoncologist.2011-0184
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study was to describe the clinical use of bevacizumab in Lombardy (9.5 million inhabitants), Italy, during 2006-2007 in patients with metastatic colorectal cancer (mCRC) to evaluate compliance with the Italian Medicine Agency (AIFA) indications, the incidence of adverse events, and the survival rate. We performed computerized record linkage among three different Lombardy health care databases: File F registry, Regional discharge database, and Registry Office records. Patients were classified into approved and off-label uses according to the AIFA indications. Treatment with bevacizumab was administered to 780 patients, of whom 81.7% (n = 637) had mCRC. Among these, 37.8% (n = 241) of patients received the drug in observance of AIFA indications. Overall, similar to 10% of patients had serious treatment-related toxicities (fistula, 3.5%; venous thromboembolism, 2.8%; hemorrhage, 1.9%; intestinal perforation and arterial thromboembolism, <1%). The 1-year survival rate was 74.3% and the 2-year survival rate was 39.2%. The median survival time was 20.5 months, and there were no meaningful differences between gender and age groups. There was a gap between the bevacizumab approved indication and clinical practice pattern: overall, less than one half of the patients received bevacizumab in observance with the regulatory indication. The main reason for nonadherence to the indication was use as a second-line or advanced line of therapy. The incidence of serious adverse events and the survival rates of mCRC patients were similar to those reported in clinical trials. The Oncologist 2012; 17: 117-124
引用
收藏
页码:117 / 124
页数:8
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