Skin cancer precursor immunotherapy for squamous cell carcinoma prevention

被引:70
|
作者
Rosenberg, Abby R. [1 ]
Tabacchi, Mary [1 ]
Ngo, Kenneth H. [2 ,3 ,4 ,5 ]
Wallendorf, Michael [6 ]
Rosman, Ilana S. [1 ,7 ]
Cornelius, Lynn A. [1 ]
Demehri, Shadmehr [2 ,3 ,4 ,5 ]
机构
[1] Washington Univ, Sch Med, Dept Med, Div Dermatol, St Louis, MO 63110 USA
[2] Massachusetts Gen Hosp, Dept Dermatol, Ctr Canc Immunol, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Dept Dermatol, Cutaneous Biol Res Ctr, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Ctr Canc Res, Boston, MA 02114 USA
[5] Harvard Med Sch, Boston, MA 02115 USA
[6] Washington Univ, Sch Med, Div Biostat, St Louis, MO 63110 USA
[7] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
关键词
THYMIC STROMAL LYMPHOPOIETIN; MALIGNANT-TRANSFORMATION; KERATINOCYTE; RISK; CHEMOPREVENTION; ENVIRONMENT; 5-PERCENT; KERATOSES; BURDEN; CREAM;
D O I
10.1172/jci.insight.125476
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BACKGROUND. 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. METHODS. 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. RESULTS. 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 SEC 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 [35% 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. CONCLUSION. 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.
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页数:10
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