Isufi Daniel, Schwarz Christopher Willy, Jensen Mikkel Bak, Seidelin Jakob, Skov Lone, Loft Nikolai
Department of Dermatology and Allergy, Copenhagen University Hospital - Herlev and Gentofte, Copenhagen, Denmark.
Copenhagen Research Group for Inflammatory Skin, Herlev and Gentofte Hospital, Herlev, Denmark.
Clin Exp Med. 2025 Jun 25;25(1):219. doi: 10.1007/s10238-025-01738-4.
While biologics have proven to be effective in treating immune-mediated inflammatory diseases (IMIDs), the label of most biologics carries a warning regarding their use in patients with active cancer or a history of cancer. Consequently, there has been a reluctance to prescribe these medications to patients with a history of cancer, and little is known about the risk of new and/or recurrent cancer in patients with IMIDs treated with biologics and a previous cancer. This systematic review and meta-analysis searched PubMed, Embase, Cochrane Library, and Web of Science up to February 23, 2024, for studies on the risk of new and/or recurrent cancer following treatment with biologics in patients with IMIDs and a previous cancer compared to controls (PROSPERO; CRD42024516899). Controls included patients receiving non-biological or no therapy. Risk estimates were calculated with random-effects meta-analysis with I statistics to estimate between-study heterogeneity. In total, 20 articles comprising 4736 patients treated with biologics with 15,646 patient-years of follow-up were included. Treatment with tumor necrosis factor (TNF)-α inhibitors (TNFi), interleukin (IL)-12/23 inhibitors or vedolizumab did not appear to lead to increased risk of new or recurrent cancer in patients with IMIDs and a previous cancer compared to conventional systemics or no therapy. The results are reassuring to patients and physicians prescribing biologics to patients with IMIDs. However, further studies are needed especially on newer biologics and decision on initiation of biologics in patients with cancers should be based on an individual assessment.
虽然生物制剂已被证明在治疗免疫介导的炎症性疾病(IMIDs)方面有效,但大多数生物制剂的标签都带有关于其在患有活动性癌症或有癌症病史的患者中使用的警告。因此,一直不愿意给有癌症病史的患者开这些药物,而且对于接受生物制剂治疗且有既往癌症史的IMIDs患者发生新发和/或复发性癌症的风险知之甚少。这项系统评价和荟萃分析检索了截至2024年2月23日的PubMed、Embase、Cochrane图书馆和Web of Science,以查找关于与对照组相比,有既往癌症史的IMIDs患者接受生物制剂治疗后发生新发和/或复发性癌症风险的研究(PROSPERO;CRD42024516899)。对照组包括接受非生物治疗或未接受治疗的患者。采用随机效应荟萃分析和I统计量计算风险估计值,以估计研究间的异质性。总共纳入了20篇文章,包括4736例接受生物制剂治疗的患者,随访时间为15646患者年。与传统全身治疗或未治疗相比,肿瘤坏死因子(TNF)-α抑制剂(TNFi)、白细胞介素(IL)-12/23抑制剂或维多珠单抗治疗似乎不会增加有既往癌症史的IMIDs患者发生新发或复发性癌症的风险。这些结果让患者和给IMIDs患者开生物制剂的医生放心。然而,尤其需要对更新的生物制剂进行进一步研究,并且对于癌症患者启动生物制剂治疗的决策应基于个体评估。