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Treatment of alopecia areata with Diphenylcyclopropenone: methodology based on the principles of allergic contact dermatitis* * Study conducted at the Clínica de Dermatologia, Irmandade da Santa Casa de Misericórdia de São Paulo, São Paulo, SP, Brazil.

Dear Editor,

Diphenylcyclopropenone (DPCP) is a chemical substance that induces a cellular immune response and, therefore, allergic contact dermatitis (ACD). Its action is based on the concept of antigenic competition, inducing the formation of TCD8 lymphocytes, which inhibit the active perifollicular immune response, allowing hair growth.11 Rokhsar CK, Shupack JL, Vafai JJ, Washenik K. Efficacy of topical sensitizers in the treatment of alopecia areata. J Am Acad Dermatol. 1998;39:751-61.

DPCP is a therapeutic for alopecia areata (AA), especially in extensive cases, with a variable response, but repilation rates in more than 50% of cases.11 Rokhsar CK, Shupack JL, Vafai JJ, Washenik K. Efficacy of topical sensitizers in the treatment of alopecia areata. J Am Acad Dermatol. 1998;39:751-61. Side effects are common, sometimes severe, such as acute eczematous reactions, in addition to lymphadenopathy, pruritus, hyperpigmentation, and flu-like symptoms, among others.22 Lee S, Kim BJ, Lee YB, Lee WS. Hair regrowth outcomes of contact immunotherapy for patients with alopecia areata: a systematic review and meta-analysis. JAMA Dermatol. 2018;154:1145-51.

Drug utilization varies, lacking methodological standardization.22 Lee S, Kim BJ, Lee YB, Lee WS. Hair regrowth outcomes of contact immunotherapy for patients with alopecia areata: a systematic review and meta-analysis. JAMA Dermatol. 2018;154:1145-51.

3 Choe AJ, Lee S, Pi LQ, Keum DI, Lee CH, Kim BJ, et al. Subclinical sensitization with diphenylcyclopropenone is sufficient for the treatment of alopecia areata: retrospective analysis of 159 cases. J Am Acad Dermatol. 2018;78:515-21.
-44 Strazzulla LC, Wang EHC, Avila L, Sicco KL, Brinster N, Christiano AM, et al. Alopecia areata: an appraisal of new treatment approaches and overview of current therapies. J Am Acad Dermatol. 2018;78:15-24. This service uses a methodology based on the principles of ACD. This case report aims to demonstrate the steps of DPCP use in AA. This standardization allowed comparing data and reducing side effects due to drug inappropriate use.

The product is purchased at 2% in acetone and stored in the refrigerator in a dark bottle. The dilutions are prepared during the appointments and applied weekly with moistened flexible swabs.

A 44-year-old male with universal AA was sensitized with 2% DPCP on 2 × 2 cm filter paper on the back for 48 hours, inducing the ACD induction phase. After 2 weeks, he was submitted to a patch test with DPCP, at 0.1%; 0.05%, and 0.02% concentrations, with readings after 48 and 96 hours, and responses 3+, 2+ and 2+ (Fig. 1) respectively, according to the previously established standardization. The 0.02% concentration was used on the scalp, where it remained covered and unwashed for 48 hours. The concentration was increased weekly to 0.1% when moderate pruritus and erythema were obtained. Repilation was acceptable after 24 weeks, without severe reactions (Fig. 2).

Figure 1
Reading of the patch test after 72 hours.

Figure 2
(A), At start of treatment; (B), after 24 weeks of DPCP treatment.

The patch test assesses whether there was sensitization to the product and predicts the best concentration with which to start treatment, choosing the one with the lowest positivity, minimizing adverse effects. If the responses are intense, the concentrations are reduced, and sometimes the applications are spaced out at intervals of two to four weeks. The concentrations depend on the response of each individual.

Therapeutic failure, that is, the absence of repilation, is considered after 180 days of regular application. If there is a response, the applications are maintained until the best possible effect is attained (up to one year).

DPCP is a drug that provides good response rates in severe cases; however, the protocols are not yet standardized. Due to common and sometimes severe side effects, strict monitoring of sensitization and control of the concentrations are necessary throughout the treatment. Moreover, no industry manufactures DPCP in accordance with regulatory standards for drug development.55 Bulock KG, Cardia JP, Pavco PA, Levis WR. Diphencyprone treatment of alopecia areata: postulated mechanism of action and prospects for therapeutic synergy with RNA interference. J Investig Dermatol Symp Proc. 2015;17:16-8. In the present environment, there is no regulation for its use, although it has been part of the therapeutic arsenal for AA treatment for many years.

  • Financial support
    None declared.

References

  • 1
    Rokhsar CK, Shupack JL, Vafai JJ, Washenik K. Efficacy of topical sensitizers in the treatment of alopecia areata. J Am Acad Dermatol. 1998;39:751-61.
  • 2
    Lee S, Kim BJ, Lee YB, Lee WS. Hair regrowth outcomes of contact immunotherapy for patients with alopecia areata: a systematic review and meta-analysis. JAMA Dermatol. 2018;154:1145-51.
  • 3
    Choe AJ, Lee S, Pi LQ, Keum DI, Lee CH, Kim BJ, et al. Subclinical sensitization with diphenylcyclopropenone is sufficient for the treatment of alopecia areata: retrospective analysis of 159 cases. J Am Acad Dermatol. 2018;78:515-21.
  • 4
    Strazzulla LC, Wang EHC, Avila L, Sicco KL, Brinster N, Christiano AM, et al. Alopecia areata: an appraisal of new treatment approaches and overview of current therapies. J Am Acad Dermatol. 2018;78:15-24.
  • 5
    Bulock KG, Cardia JP, Pavco PA, Levis WR. Diphencyprone treatment of alopecia areata: postulated mechanism of action and prospects for therapeutic synergy with RNA interference. J Investig Dermatol Symp Proc. 2015;17:16-8.

Publication Dates

  • Publication in this collection
    18 Feb 2022
  • Date of issue
    2022

History

  • Received
    02 June 2020
  • Accepted
    11 Aug 2020
  • Published
    06 Dec 2021
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