Levine Jasmine, Islam Rahib K, Mo Lillian, Maltese Alexander, Adalsteinsson Jonas, Talia Jordan, Gulati Nicholas, Ungar Benjamin
Department of Dermatology, Icahn School of Medicine at Mount Sinai, 5 East 98th Street, New York, NY, 10029, USA.
Louisiana State University Health Sciences Center New Orleans School of Medicine, New Orleans, LA, 70112, USA.
Arch Dermatol Res. 2025 May 14;317(1):757. doi: 10.1007/s00403-025-04258-z.
Alopecia areata (AA) is an autoimmune hair loss disorder, with Janus kinase inhibitors (JAKis) emerging as an effective treatment. However, concerns about malignancy risk remain due to boxed warnings primarily based on studies in rheumatoid arthritis. This retrospective cohort study evaluated the association between JAKis and malignancy risk in AA using the TriNetX Global Collaborative Network. Patients with severe AA were categorized by treatment history, including JAKis, traditional immunosuppressants, and no systemic treatment. Propensity score-matched Cox proportional hazards models assessed the risks of squamous cell carcinoma (SCC)/basal cell carcinoma (BCC), internal malignancies, and hematologic malignancies. Among matched cohorts of 920 patients treated with traditional immunosuppressants and 920 treated with JAKis (mean follow-up: 1,302 and 1,229 days, respectively), SCC/BCC risk was not significantly different (HR = 0.324 [0.065, 1.609]). However, internal malignancy (HR = 4.906 [2.168, 11.101]) and hematologic malignancy (HR = 8.713 [1.104, 68.796]) risks were significantly higher with traditional immunosuppressants. No significant difference in malignancy risk was observed between 446 JAKi-treated and 446 untreated patients. These findings align with previous meta-analyses in autoimmune diseases, which have not linked JAKis to an increased malignancy risk. While this study found no evidence that JAKis elevate malignancy risk, the role of JAK-STAT signaling in cancer remains complex. Given AA's unclear baseline malignancy risk and this study's retrospective nature and limited follow-up, longer-term studies are needed to better understand the long-term safety of JAKis in AA and refine risk assessment and screening strategies.
斑秃(AA)是一种自身免疫性脱发疾病,Janus激酶抑制剂(JAKis)已成为一种有效的治疗方法。然而,由于主要基于类风湿关节炎研究的黑框警告,对恶性肿瘤风险的担忧仍然存在。这项回顾性队列研究使用TriNetX全球合作网络评估了JAKis与AA患者恶性肿瘤风险之间的关联。重度AA患者根据治疗史进行分类,包括使用JAKis、传统免疫抑制剂以及未进行全身治疗。倾向评分匹配的Cox比例风险模型评估了鳞状细胞癌(SCC)/基底细胞癌(BCC)、内部恶性肿瘤和血液系统恶性肿瘤的风险。在920例接受传统免疫抑制剂治疗和920例接受JAKis治疗的匹配队列中(平均随访时间分别为1302天和1229天),SCC/BCC风险无显著差异(风险比[HR]=0.324[0.065,1.609])。然而,传统免疫抑制剂组的内部恶性肿瘤风险(HR=4.906[2.168,11.101])和血液系统恶性肿瘤风险(HR=8.713[1.104,68.796])显著更高。在446例接受JAKi治疗的患者和446例未治疗的患者之间,未观察到恶性肿瘤风险的显著差异。这些发现与先前关于自身免疫性疾病的荟萃分析一致,这些分析未将JAKis与恶性肿瘤风险增加联系起来。虽然这项研究没有发现JAKis会增加恶性肿瘤风险的证据,但JAK-STAT信号通路在癌症中的作用仍然复杂。鉴于AA的基线恶性肿瘤风险不明确,以及本研究的回顾性性质和有限的随访时间,需要进行长期研究,以更好地了解JAKis在AA中的长期安全性,并完善风险评估和筛查策略。