Department of Rheumatology and Immunology, West China Hospital, Sichuan University, 37 Guoxue Xiang, Chengdu, Sichuan 610041, China.
Division of Arthritis and Rheumatic Diseases, Oregon Health & Science University, Portland, OR 97239, United States.
Cytokine. 2018 Jan;101:78-88. doi: 10.1016/j.cyto.2016.09.013. Epub 2016 Sep 26.
Inhibition of tumor necrosis factor (TNF) activity has profoundly changed the management of several immune-mediated inflammatory diseases with great benefit for patients. The application of TNF inhibitors (TNFi), however, also brings a new concern, malignancy. We performed a systemic review to collect the studies reporting cancer incidences and risks in TNFi users regardless of indications. TNFi were most frequently used in treating patients with rheumatoid arthritis (RA) and inflammatory bowel diseases (IBD). In RA patients without prior cancer history, the incidences of malignancies ranged from the lowest rate 0 per 1000 person-years in etanercept users regarding lymphoma to the highest rate 35.62 per 1000 person-years in adalimumab users on non-melanoma skin cancer (NMSC), while in those patients with prior cancer history, the recurrent incidences of malignancies ranged from the lowest rate 5.05 per 1000 person-years regarding melanoma to the highest rate 63.20 per 1000 person-years on basal cell carcinoma (BCC) in TNFi users. In IBD patients, incidences ranged from 0 per 1000 person-years in TNFi users on lymphoma to 34.0 per 1000 person-years in infliximab users on overall cancer. However, these incidence rates of overall cancer, lymphoma and melanoma were not higher in comparison with those patients who were not treated with TNFi. Compared to general population, incidences of lymphoma were elevated in RA patients and rates of NMSC were higher in patients with psoriasis, RA and IBD. In conclusion, cancer incidences vary across different studies, indications, cancer types and studies with different individual TNFi. Treatment with TNFi is not associated with increased malignant risks of overall cancer, lymphoma or melanoma. Results of NMSC risk were inconsistent among studies. A latest prospective registry study demonstrated a small increased risk of squamous cell cancer in RA patients treated with TNFi (one additional case for every 1600years of treatment experience). Further prospective studies are needed to verify whether TNFi users have higher NMSC risk than non-TNFi users.
肿瘤坏死因子(TNF)活性的抑制极大地改变了几种免疫介导的炎症性疾病的治疗方法,使患者受益匪浅。然而,TNF 抑制剂(TNFi)的应用也带来了一个新的关注点,即恶性肿瘤。我们进行了系统评价,以收集报告 TNFi 使用者(无论适应证如何)癌症发病率和风险的研究。TNFi 最常用于治疗类风湿关节炎(RA)和炎症性肠病(IBD)患者。在没有既往癌症史的 RA 患者中,恶性肿瘤的发病率从依那西普使用者最低的每 1000 人年 0 例(淋巴瘤)到阿达木单抗使用者非黑色素瘤皮肤癌(NMSC)的最高每 1000 人年 35.62 例,而在有既往癌症史的患者中,恶性肿瘤的复发性发病率从黑色素瘤的最低每 1000 人年 5.05 例到 TNFi 使用者基底细胞癌(BCC)的最高每 1000 人年 63.20 例。在 IBD 患者中,TNFi 使用者的淋巴瘤发病率为 0 例,总体癌症发病率为 34.0 例。然而,与未接受 TNFi 治疗的患者相比,这些总体癌症、淋巴瘤和黑色素瘤的发病率并没有更高。与普通人群相比,RA 患者的淋巴瘤发病率升高,银屑病、RA 和 IBD 患者的 NMSC 发病率更高。总之,不同研究、适应证、癌症类型和使用不同个体 TNFi 的研究之间,癌症发病率存在差异。TNFi 治疗与总体癌症、淋巴瘤或黑色素瘤恶性风险增加无关。NMSC 风险的研究结果不一致。一项最新的前瞻性登记研究表明,TNFi 治疗的 RA 患者鳞状细胞癌的风险略有增加(每 1600 年治疗经历增加一例)。需要进一步的前瞻性研究来验证 TNFi 使用者的 NMSC 风险是否高于非 TNFi 使用者。