Real‐world effectiveness of adalimumab in patients with moderate‐to‐severe hidradenitis suppurativa: the 1‐year SOLACE study

Background Long‐term, real‐word data are needed to help manage patients with hidradenitis suppurativa (HS) through this recurrent, painful and debilitating disease. Objectives To primarily measure real‐world effectiveness of adalimumab in HS and to secondarily observe clinical course of HS in the li...

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Published inJournal of the European Academy of Dermatology and Venereology Vol. 35; no. 12; pp. 2431 - 2439
Main Authors Gulliver, W., Alavi, A., Wiseman, M.C., Gooderham, M.J., Rao, J., Alam, M.S., Papp, K.A., Desjardins, O., Jean, C.
Format Journal Article
LanguageEnglish
Published Hoboken John Wiley and Sons Inc 01.12.2021
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Summary:Background Long‐term, real‐word data are needed to help manage patients with hidradenitis suppurativa (HS) through this recurrent, painful and debilitating disease. Objectives To primarily measure real‐world effectiveness of adalimumab in HS and to secondarily observe clinical course of HS in the light of patients’ response. Methods In SOLACE, adults with moderate‐to‐severe HS in need for change in ongoing therapy were treated with adalimumab for up to 52 weeks as per physician’s medical practice. Treatment effectiveness was measured by Hidradenitis Suppurativa Clinical Response (HiSCR). Inflammatory nodules, abscesses and draining fistulas were counted, Hurley stage was assessed, and disease severity was rated using the International HS Severity Scoring System (IHS4). A post hoc analysis further explored the HiSCR response by abscess and inflammatory nodule (AN) count at baseline (low, medium and high) and gender. Spontaneously reported safety events were collected. Results From 23 Canadian centres, 69% of the 138 patients achieved HiSCR at week 24, which increased to 82% and 75% at week 52 in patients with medium and high AN counts, respectively. Gender (4 times the odds for female) and age at HS onset (5% decrease with each additional year) had an effect on achieving HiSCR. Treatment with adalimumab led to an important decrease in number of lesions in responders, with most gains observed in inflammatory nodules, more frequently in the lower body area of patients in the high AN count group. The IHS4 scores of responders were substantially lowered, with a larger decrease in patients of the high AN count group. No new safety signal was detected. Conclusions The effectiveness of adalimumab was maintained during this 1‐year period, and an optimal gain was documented for patients with medium and high AN counts. These real‐world data support a prompt treatment of HS patients and the use of IHS4 to monitor treatment.
Bibliography:Funding sources
Honoraria were received either in support of the present manuscript or from the past 36 months in relation to the content of the manuscript. Dr Gulliver received grants from AbbVie, Actelion, Amgen, Asana Biosciences, Arylide, Astellas, Bausch Health, Boehringer Ingelheim, Celgene, Cipher, Corrona/National Psoriasis Foundation, Devinian, Eli Lilly, Galapagos, Galderma, Janssen, LEO Pharma, Merck, Novartis, PeerVoice, Pfizer, Regeneron, Sanofi‐Genzyme, Tribute, UCB and Valeant. Dr Gooderham received grants from AbbVie, Novartis and UCB. Dr Papp received grants from AbbVie, Akros, Amgen, Anacor, Arcutis, Astellas, Avillion, Bausch Health/Valeant, Baxalta, Boehringer Ingelheim, Bristol‐Myers Squibb, Can‐Fite Biopharma, Celgene, Coherus, Dermavant, Dermira, Dice Pharmaceuticals, Dow Pharma, Eli Lilly, Evelo, Galapagos, Galderma, Genentech, Gilead, GSK, Incyte, Janssen, Kyowa Hakko Kirin, Leo, MedImmune, Meiji Seika Pharma, Merck (MSD), Merck Serono, Mitsubishi Pharma, Moberg Pharma, Novartis, Pfizer, PRCL Research, Regeneron, Roche, Sanofi‐Aventis/Genzyme, Sun Pharma, Takeda and UCB. Mr Desjardins received grants from AbbVie. Dr Jean received grants from AbbVie. Dr Alavi, Dr Wiseman, Dr Rao and Dr Alam declared no conflict of interest.
Conflict of interest
AbbVie sponsored the study; contributed to the design; and participated in the collection, analysis and interpretation of data, as well as in writing, reviewing and approving the final version of this manuscript. No honoraria or payments were made for authorship.
Linked Commentary: R.S. Gibson and A.B. Kimball. J Eur Acad Dermatol Venereol 2021; 35: 2342. https://doi.org/10.1111/jdv.17741.
ISSN:0926-9959
1468-3083
DOI:10.1111/jdv.17598