Biancone Livia, Calabrese Emma, Petruzziello Carmelina, Pallone Francesco
Università Tor Vergata of Rome, Italy.
Nat Clin Pract Gastroenterol Hepatol. 2007 Feb;4(2):78-91. doi: 10.1038/ncpgasthep0695.
The proven involvement of cytokines in the pathophysiology of IBD has led to the development of powerful, selective, anticytokine drugs--so-called biologics--as a therapy for IBD. Although the efficacy of infliximab, a chimeric monoclonal IgG1 antibody directed against tumor necrosis factor, is proven and the use of biologic agents is growing worldwide, there is concern about their long-term safety, which includes the risk of developing cancer. An increased risk of malignancies, particularly lymphoma, has been reported in some studies of infliximab-treated patients with IBD; however, the increased risk could be caused by the underlying chronic disease, severity of the disease, concomitant medications (e.g. conventional immunomodulators), infliximab itself, or all of these variables. At present, the data do not provide clear evidence for a causal association between infliximab and the increased cancer risk. In appropriately selected patients with severe, refractory Crohn's disease, the benefits of biologic therapy seem to outweigh the cancer risk. Multicenter, case-control studies in large populations, with a long-term follow-up are needed to define the outcome of patients with IBD treated with biologic therapies.
细胞因子在炎症性肠病病理生理学中的明确作用促使了强效、选择性抗细胞因子药物(即所谓的生物制剂)的研发,用于治疗炎症性肠病。尽管抗肿瘤坏死因子嵌合单克隆IgG1抗体英夫利昔单抗的疗效已得到证实,且生物制剂在全球的使用也在增加,但人们对其长期安全性存在担忧,这包括患癌风险。在一些针对接受英夫利昔单抗治疗的炎症性肠病患者的研究中,已报告恶性肿瘤尤其是淋巴瘤的风险增加;然而,风险增加可能是由潜在的慢性疾病、疾病严重程度、联合用药(如传统免疫调节剂)、英夫利昔单抗本身或所有这些变量共同导致的。目前,数据并未提供英夫利昔单抗与癌症风险增加之间存在因果关系的明确证据。在适当选择的重度难治性克罗恩病患者中,生物治疗的益处似乎超过癌症风险。需要开展针对大量人群的多中心病例对照研究,并进行长期随访,以明确接受生物治疗的炎症性肠病患者的预后情况。