4.4 Article

A novel approach for wound treatment using dried cultured epidermal allograft: A phase I/II, single-center, open-label clinical trial

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BURNS
卷 49, 期 5, 页码 1079-1086

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ELSEVIER SCI LTD
DOI: 10.1016/j.burns.2022.10.006

关键词

Cultured epidermis; Cultured keratinocyte sheet; Cultured epidermal allograft; Feasibility study; Clinical study; Burn; Wound healing

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A prospective clinical study was conducted to confirm the safety and efficacy of dried allogeneic cultured epidermis (CE) for wound treatment. The results showed that treatment with dried CE was effective in promoting wound healing and had a low incidence of severe adverse events.
Background: Autologous cultured epidermis (CE) is successfully used in burn care, but it requires a manufacturing time of three weeks and is very expensive owing to its custommade nature of treatment. To compensate this disadvantage, dried allogeneic CE promises a novel therapeutic approach; and previous reports have demonstrated its efficacy in promoting wound healing using a murine skin defect model. Herein, a prospective clinical study was conducted to confirm the safety and efficacy of dried allogeneic CE for wound treatment. Methods: Dried CE was manufactured using donor keratinocytes obtained from excess surgical skin and applied to skin defects that were at least 3 cm in length and less than 10 % of the body surface area of the patients. The patients were observed for 14 days after CE application. The primary endpoint was the incidence of adverse events and the secondary endpoint was the percentage of wound healed since baseline, on days 7 and 14. Furthermore, as a stratified analysis, the percentage of wound healed, specified as deep dermal burns, was calculated. Results: Six patients (five burns and one skin ulcer after necrotizing fasciitis) enrolled in the study. As a serious adverse event, a local infection was observed in one patient, which resolved by debridement and conventional skin grafting. Other adverse events that were potentially related to this treatment included two cases of skin erosion, and one case of systemic fever. No unresolved adverse events remained at the end of the study period. The percentage of wound healed was 73.4 & PLUSMN; 19.2 % on Day 7, and 92.2 & PLUSMN; 11.8 % on Day 14. When the targeted disease was restricted to deep dermal burns, the percentage of wound healed was 69.9 & PLUSMN; 28.9 % on Day 7 and 90.5 & PLUSMN; 13.2 % on Day 14. Conclusion: Treatment with dried CE was safely performed without any unresolved severe adverse effects. Dried CE is a new and promising modality for skin defect treatment, such

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