Department of Epidemiology, Istituto di Ricerche Farmacologiche Mario Negri, via Giuseppe La Masa 19, 20156 Milan, Italia.
Oncologist. 2012;17(1):117-24. doi: 10.1634/theoncologist.2011-0184. Epub 2011 Dec 30.
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, ∼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.
本研究旨在描述贝伐珠单抗在意大利伦巴第地区(950 万居民)的临床应用,以评估转移性结直肠癌(mCRC)患者在 2006-2007 年期间对意大利药品管理局(AIFA)适应证的依从性、不良反应发生率和生存率。我们对伦巴第地区的三个不同卫生保健数据库(File F 登记处、地区出院数据库和登记处记录)进行了计算机记录链接。根据 AIFA 适应证,将患者分为批准适应证和超适应证使用。共对 780 例患者使用了贝伐珠单抗治疗,其中 81.7%(n=637)为 mCRC。在这些患者中,37.8%(n=241)的患者按照 AIFA 适应证使用了该药物。总体而言,约 10%的患者出现严重的治疗相关毒性(瘘管 3.5%;静脉血栓栓塞 2.8%;出血 1.9%;肠穿孔和动脉血栓栓塞 <1%)。1 年生存率为 74.3%,2 年生存率为 39.2%。中位生存时间为 20.5 个月,性别和年龄组之间无显著差异。贝伐珠单抗的批准适应证与临床实践模式之间存在差距:总体而言,不到一半的患者按照监管适应证使用了贝伐珠单抗。不遵守适应证的主要原因是将其作为二线或晚期治疗方案。mCRC 患者严重不良事件的发生率和生存率与临床试验报告的相似。