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Phototoxicity of B-RAF inhibitors: Exclusively due to UVA radiation and rapidly regressive

  • Investigative Report
  • Published:
European Journal of Dermatology Aims and scope

Abstract

Background

New targeted melanoma therapies such as B-RAF inhibitors have shown high and promising clinical benefit but have cutaneous side-effects, including photosensitivity, which is triggered in the UVA radiation spectrum. However, visible spectrum implication has not yet been investigated.We conducted a study to determine whether visible light also contributes to the phototoxicity action spectrum of vemurafenib. The secondary end points were to determine the time to complete regression of the phototoxicity post-vemurafenib discontinuation and whether there was a significant difference between the UVA radiation immediate reactivity cut-offs, in patients treated with vemurafenib vs. those treated with dabrafenib.

Method

This prospective, observational study included patients with B-RAF mutant metastatic melanoma: 34 patients treated with vemurafenib and 9 with dabrafenib.

Results

The visible-light phototest results in patients treated with vemurafenib were all negative before and after 2 months of treatment. The UVA radiation phototests conducted 1 or 2 weeks post-vemurafenib discontinuation in 4 patients showed a normalised UVA-radiation reactivity cut-off. UVA radiation phototests after 2 months of treatment were conducted for all patients. The UVA radiation reactivity cut-off had been lowered for 30 patients (88%) on vemurafenib and 3 patients (33%) on dabrafenib. The median UVA radiation reactivity cut-off was 12 J/cm2 for the patients on vemurafenib and 20 J/cm2 for the patients on dabrafenib.

Conclusion

B-RAF inhibitor phototoxicity is exclusively triggered byUVAradiation and resolves rapidly post-treatment discontinuation. A significant difference between the UVA immediate reactivity cut-offs, vemurafenib vs. dabrafenib, explains the difference in the clinical photosensitivity rates reported in the clinical trials.

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References

  1. Chapman PB, Hauschild A, Robert C, et al. Improved survival with vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med 2011; 364: 2507–16.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  2. Hauschild A, Grob J-J, Demidov LV, et al. Dabrafenib in BRAFmutated metastatic melanoma: a multicentre, open-label, phase 3 randomised controlled trial. Lancet 2012; 380: 358–65.

    Article  PubMed  CAS  Google Scholar 

  3. Anforth R, Fernandez-Pe˜nas P, Long GV. Cutaneous toxicities of RAF inhibitors. Lancet Oncol 2013; 14: e11–8.

    Article  PubMed  CAS  Google Scholar 

  4. Flaherty KT, Puzanov I, Kim KB, et al. Inhibition of mutated, activated BRAF in metastatic melanoma. N Engl J Med 2010; 363: 809. 19.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  5. Sosman JA, Kim KB, Schuchter L, et al. Survival in BRAF V600-mutant advanced melanoma treated with vemurafenib. N Engl J Med 2012; 366: 707–14.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  6. Ascierto PA, Minor D, Ribas A, et al. Phase II trial (BREAK-2) of the BRAF inhibitor dabrafenib (GSK2118436) in patients with metastatic melanoma. J Clin Oncol 2013; 31: 3205–11.

    Article  PubMed  CAS  Google Scholar 

  7. Dummer R, Rinderknecht J, Goldinger SM. Ultraviolet A and photosensitivity during vemurafenib therapy. N Engl J Med 2012; 366: 480. 1.

    Article  PubMed  CAS  Google Scholar 

  8. Gelot P, Dutartre H, Khammari A, et al. Vemurafenib: an unusual UVA-induced photosensitivity. Exp Dermatol 2013; 22: 297–8.

    Article  PubMed  CAS  Google Scholar 

  9. Brugière C, Stefan A, Morice C, Cornet E, Moreau A, Allouche S, et al. Vemurafenib skin phototoxicity is indirectly linked to ultraviolet A minimal erythema dose decrease. Br J Dermatol 2014; 171: 1529–32.

    Article  PubMed  Google Scholar 

  10. Du-Thanh A, Debu A, Lalheve P, Guillot B, Dereure O, Peyron J-L. Solar urticaria: a time-extended retrospective series of 61 patients and review of literature. Eur J Dermatol 2013; 23: 202–7.

    PubMed  Google Scholar 

  11. Boussemart L, Routier E, Mateus C, et al. Prospective study of cutaneous side-effects associated with the BRAF inhibitor vemurafenib: a study of 42 patients. Ann Oncol 2013; 24: 1691–7.

    Article  PubMed  CAS  Google Scholar 

  12. Mattei PL, Alora-Palli MB, Kraft S, Lawrence DP, Flaherty KT, Kimball AB. Cutaneous effects of BRAF inhibitor therapy: a case series. Ann Oncol 2013; 24: 530–7.

    Article  PubMed  CAS  Google Scholar 

  13. Moseley H, Naasan H, Dawe RS, Woods J, Ferguson J. Population reference intervals for minimal erythemal doses in monochromator phototesting. Photodermatol Photoimmunol Photomed 2009; 25: 8–11.

    Article  PubMed  Google Scholar 

  14. Béani JC. [Interpretation of photobiologic tests]. Ann Dermatol Venereol 1987; 114: 123–6.

    PubMed  Google Scholar 

  15. Committee for Medicinal Products for Human Use (CHMP). Assessment Report of Zelboraf, vemurafenib. EMA/CHMP/926998/2011. 2011.

    Google Scholar 

  16. FDA/Center for Drug Evaluation and Research, Division of Drug Oncology Products (HFD-150) 2011. Pharmacology and Toxicology NDA Review and Evaluation of Zelboraf, vemurafenib. 2011.

    Google Scholar 

  17. Boudon SM, Plappert-Helbig U, Odermatt A, Bauer D. Characterization of vemurafenib phototoxicity in a mouse model. Toxicol Sci Off J Soc Toxicol 2014; 137: 259–67.

    Article  CAS  Google Scholar 

  18. Shah N, Iyer RM, Mair H-J, et al. Improved human bioavailability of vemurafenib, a practically insoluble drug, using an amorphous polymer-stabilized solid dispersion prepared by a solvent-controlled coprecipitation process. J Pharm Sci 2013; 102: 967–81.

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Brigitte Dreno.

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Gabeff, R., Dutartre, H., Khammari, A. et al. Phototoxicity of B-RAF inhibitors: Exclusively due to UVA radiation and rapidly regressive. Eur J Dermatol 25, 452–456 (2015). https://doi.org/10.1684/ejd.2015.2628

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  • DOI: https://doi.org/10.1684/ejd.2015.2628

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