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Effective and durable repigmentation for stable vitiligo: A randomized within-subject controlled trial assessing treatment with autologous skin cell suspension transplantation - 20/11/24

Doi : 10.1016/j.jaad.2024.08.027 
Iltefat H. Hamzavi, MD a, , Anand K. Ganesan, MD, PhD b, Bassel H. Mahmoud, MD, PhD c, Eduardo Weiss, MD d, Ammar M. Ahmed, MD e, Deanne Robinson, MD f, Mitchel P. Goldman, MD g, Girish Munavalli, MD h, Steven A. Kahn, MD i, Victor Huang, MD j, Jill Waibel, MD k, Alpesh Desai, DO l, Nada Elbuluk, MD, MSc m, Seemal Desai, MD n, o, Amit G. Pandya, MD p
a Department of Dermatology, Henry Ford Health System, Dermatology Research, Detroit, Michigan 
b Department of Dermatology, University of California Irvine, Irvine, California 
c Department of Dermatology, University of Massachusetts, Worcester, Massachusetts 
d Skin Care Research, Hollywood, Florida 
e Department of Internal Medicine, Dell Medical School at the University of Texas at Austin, Austin, Texas 
f DMR Research PLLC, Westport, Connecticut 
g Cosmetic Laser Dermatology: A Platinum Dermatology Partners Company, San Diego, California 
h Dermatology, Laser, & Vein Specialists of the Carolinas, Charlotte, North Carolina 
i Department of Surgery, Medical University of South Carolina, Charleston, South Carolina 
j Department of Dermatology, University of California, Sacramento, California 
k Miami Dermatology & Laser Research, Miami, Florida 
l Heights Dermatology & Aesthetic Center, Houston, Texas 
m Department of Dermatology, Keck School of Medicine USC, Los Angeles, California 
n Innovative Dermatology, Plano, Texas 
o Department of Dermatology, The University of Texas Southwestern Medical Center, Dallas, Texas 
p Palo Alto Foundation Medical Group, Sunnyvale, California 

Correspondence to: Iltefat H. Hamzavi, MD, Henry Ford Health System, Dermatology Research, 3031 W Grand Blvd, Detroit, MI 48202.Henry Ford Health SystemDermatology Research3031 W Grand BlvdDetroitMI48202

Abstract

Background

Vitiligo lesions are often challenging to repigment with conventional medical therapies. Surgical autologous melanocyte transfer methods can be utilized for stable vitiligo but demand specialized skills and equipment. A point-of-care autologous cell harvesting device was designed enabling simple preparation of autologous skin cell suspension (ASCS) containing melanocytes, keratinocytes, and fibroblasts providing a straightforward approach for cellular transplantation.

Objective

To evaluate the safety and effectiveness of ASCS for repigmentation of stable vitiligo lesions among adults.

Methods

A US multicenter, randomized, within-subject controlled trial compared ASCS to narrow band ultraviolet B only (Control) in similar vitiligo lesions. ASCS was applied after laser skin resurfacing and followed by narrow band ultraviolet B treatment. The primary effectiveness endpoint was the proportion of lesions achieving ≥80% repigmentation at week-24. Repigmentation durability was assessed at week-52.

Results

Among 25 subjects, 36% of ASCS-treated lesions achieved ≥80% repigmentation at week-24 compared to 0% for Control (P < .025), with durability through week-52. The safety profile of ASCS was acceptable, with favorable patient- and investigator-reported outcomes.

Limitations

Study sample size limited robust subgroup analyses.

Conclusion

Application of ASCS has potential as a treatment for repigmentation of stable vitiligo lesions with the potential to improve health-related quality of life and reduce burden of disease.

Il testo completo di questo articolo è disponibile in PDF.

Key words : autologous cell transfer, autologous skin cell suspension, cellular grafting, melanocyte transfer, noncultured skin cell suspension, procedural dermatology, repigmentation, vitiligo, vitiligo surgery

Abbreviations used : AE, ASCS, CRC, F-VASI, FDA, MKT, US


Mappa


 Funding sources: AVITA Medical.
 Patient consent: Consent for the publication of recognizable patient photographs or other identifiable material was obtained via the informed consent process and is available upon request.
 IRB approval status: Each study site had institutional review board oversight.


© 2024  American Academy of Dermatology, Inc.. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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