Division of Dermatology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Center for Cancer Immunology and Cutaneous Biology Research Center, Department of Dermatology and Center for Cancer Research, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
JCI Insight. 2019 Mar 21;4(6). doi: 10.1172/jci.insight.125476.
Topical calcipotriol plus 5-fluorouracil (5-FU) combination is an effective immunotherapy against actinic keratosis (AK), which is a precursor to squamous cell carcinoma (SCC). However, the long-term effectiveness of calcipotriol plus 5-FU treatment for SCC prevention is unknown.
We performed a blinded prospective cohort study on participants of a randomized double-blind clinical trial in which a 4-day course of topical calcipotriol plus 5-FU combination was compared to Vaseline plus 5-FU (control) for AK treatment. SCC and basal cell carcinoma (BCC) incidences were assessed at 1, 2, and 3 years after trial. Tissues were analyzed for calcipotriol plus 5-FU-induced T cell immunity in the skin.
Calcipotriol plus 5-FU-induced tissue-resident memory T (Trm) cell formation in face and scalp skin associated with significantly higher erythema scores compared with control (P < 0.01). Importantly, more participants in the test cohort remained SCC-free over the more than 1,500-day follow-up period (P = 0.0765), and significantly fewer developed SCC on the treated face and scalp within 3 years (2 of 30 [7%] versus 11 of 40 [28%] in control group, hazard ratio 0.215 [95% CI: 0.048-0.972], P = 0.032). Accordingly, significantly more epidermal Trm cells persisted in the calcipotriol plus 5-FU-treated face and scalp skin compared with control (P = 0.0028). There was no significant difference in BCC incidence between the treatment groups.
A short course of calcipotriol plus 5-FU treatment on the face and scalp is associated with induction of robust T cell immunity and Trm formation against AKs and significantly lowers the risk of SCC development within 3 years of treatment.
This research was supported by internal academic funds and by grants from the Burroughs Wellcome Fund, Sidney Kimmel Foundation, Cancer Research Institute, and NIH.
局部钙泊三醇加 5-氟尿嘧啶(5-FU)联合治疗是一种有效的光化性角化病(AK)免疫疗法,AK 是鳞状细胞癌(SCC)的前身。然而,钙泊三醇加 5-FU 治疗预防 SCC 的长期效果尚不清楚。
我们对一项随机双盲临床试验的参与者进行了一项盲前瞻性队列研究,其中比较了为期 4 天的局部钙泊三醇加 5-FU 联合治疗与凡士林加 5-FU(对照组)治疗 AK。在试验后 1、2 和 3 年评估 SCC 和基底细胞癌(BCC)的发生率。分析组织中钙泊三醇加 5-FU 诱导的皮肤 T 细胞免疫。
钙泊三醇加 5-FU 诱导面部和头皮皮肤中的组织驻留记忆 T(Trm)细胞形成,与对照组相比,红斑评分显著升高(P < 0.01)。重要的是,在超过 1500 天的随访期间,试验组中更多的参与者保持 SCC 无病状态(P = 0.0765),并且在 3 年内治疗的面部和头皮上 SCC 的发病率明显较低(试验组 30 例中有 2 例[7%],对照组 40 例中有 11 例[28%],风险比 0.215[95%CI:0.048-0.972],P = 0.032)。相应地,与对照组相比,钙泊三醇加 5-FU 治疗的面部和头皮皮肤中持续存在的表皮 Trm 细胞明显更多(P = 0.0028)。两组 BCC 的发病率无显着差异。
面部和头皮上的短期钙泊三醇加 5-FU 治疗与 AK 的强大 T 细胞免疫和 Trm 形成有关,并显著降低治疗后 3 年内 SCC 发展的风险。
本研究得到内部学术基金以及 Burroughs Wellcome 基金、Sidney Kimmel 基金会、癌症研究所和 NIH 的资助。