Journal Article

Randomized trial of calcipotriol combined with 5-fluorouracil for skin cancer precursor immunotherapy

Cornelius, Lynn A., Turkoz, Ahu, Wallendorf, Michael, Tabacchi, Mary, Mirzaalian, Hengameh, Tuchayi, Sara Moradi, Kopan, Raphael, Eliane, Jean-Pierre, Schaffer, Andras, Demehri, Shadmehr, Manivasagam, Sindhu, Saavedra, Arturo P., Cunningham, Trevor J.

2017

Overview

Actinic keratosis is a precursor to cutaneous squamous cell carcinoma. Long treatment durations and severe side effects have limited the efficacy of current actinic keratosis treatments. Thymic stromal lymphopoietin (TSLP) is an epithelium-derived cytokine that induces a robust antitumor immunity in barrier-defective skin. Here, we investigated the efficacy of calcipotriol, a topical TSLP inducer, in combination with 5-fluorouracil (5-FU) as an immunotherapy for actinic keratosis. The mechanism of calcipotriol action against skin carcinogenesis was examined in genetically engineered mouse models. The efficacy and safety of 0.005% calcipotriol ointment combined with 5% 5-FU cream were compared with Vaseline plus 5-FU for the field treatment of actinic keratosis in a randomized, double-blind clinical trial involving 131 participants. The assigned treatment was self-applied to the entirety of the qualified anatomical sites (face, scalp, and upper extremities) twice daily for 4 consecutive days. The percentage of reduction in the number of actinic keratoses (primary outcome), local skin reactions, and immune activation parameters were assessed. Calcipotriol suppressed skin cancer development in mice in a TSLP-dependent manner. Four-day application of calcipotriol plus 5-FU versus Vaseline plus 5-FU led to an 87.8% versus 26.3% mean reduction in the number of actinic keratoses in participants (P < 0.0001). Importantly, calcipotriol plus 5-FU treatment induced TSLP, HLA class II, and natural killer cell group 2D (NKG2D) ligand expression in the lesional keratinocytes associated with a marked CD4+ T cell infiltration, which peaked on days 10-11 after treatment, without pain, crusting, or ulceration. Our findings demonstrate the synergistic effects of calcipotriol and 5-FU treatment in optimally activating a CD4+ T cell-mediated immunity against actinic keratoses and, potentially, cancers of the skin and other organs. ClinicalTrials.gov NCT02019355. Not applicable (investigator-initiated clinical trial).

• Publisher: American Society for Clinical Investigation
• Subject: Actinic keratosis / Administration, Topical / Aged / Aged, 80 and over / Animals / Antineoplastic Combined Chemotherapy Protocols - administration & dosage / Biomedical research / Calcipotriene / Calcitriol - administration & dosage / Calcitriol - analogs & derivatives / Carcinoma, Squamous Cell - drug therapy / Carcinoma, Squamous Cell - genetics / Carcinoma, Squamous Cell - immunology / Carcinoma, Squamous Cell - pathology / Care and treatment / CD4-Positive T-Lymphocytes - immunology / CD4-Positive T-Lymphocytes - pathology / Clinical Medicine / Clinical trials / Cytokines - genetics / Cytokines - immunology / Dosage and administration / Female / Fluorouracil / Fluorouracil - administration & dosage / Genetic engineering / Humans / Immunity, Cellular - drug effects / Immunity, Cellular - genetics / Immunotherapy / Inflammation / Keratosis, Actinic - drug therapy / Keratosis, Actinic - genetics / Keratosis, Actinic - immunology / Keratosis, Actinic - pathology / Male / Mice / Mice, Transgenic / Middle Aged / Precancerous Conditions - drug therapy / Precancerous Conditions - genetics / Precancerous Conditions - immunology / Precancerous Conditions - pathology / Psoriasis / Rodents / Skin cancer / Skin Neoplasms - drug therapy / Skin Neoplasms - genetics / Skin Neoplasms - immunology / Skin Neoplasms - pathology / Tumors