Literature DB >> 32564417

Systemic or biologic treatment in psoriasis patients does not increase the risk of a severe form of COVID-19.

A-C Fougerousse1, M Perrussel2, P-A Bécherel3, E Begon4, V Pallure5, I Zaraa6, G Chaby7, J Parier8,9, M Kemula10,11, L Mery-Bossard12, C Poreaux13, C Taieb14, F Maccari1,8, Z Reguiai15.   

Abstract

Entities:  

Mesh:

Substances:

Year:  2020        PMID: 32564417      PMCID: PMC7323155          DOI: 10.1111/jdv.16761

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN: 0926-9959            Impact factor:   9.228


× No keyword cloud information.
Dear Editor Some systemic and biologic psoriasis treatments [SBT] have been associated with an increased risk of infection. To date, more and more data regarding the risk of COVID‐19 infection in patients receiving SBT become available. , , , To enrich these data, we evaluated the frequency of severe COVID‐19 infections, defined as hospitalization or death, in psoriasis patients receiving SBT, especially during the 4 months following SBT initiation. From 27 April to 7 May 2020, we conducted a national, multicentre, cross‐sectional study during consultations or teleconsultations, including adult psoriasis patients receiving SBT. The following elements were collected: gender, age, current psoriasis treatment, treatment period (initiation [up to 4 months] or maintenance [from 5th month]), treatment continued or stopped during the pandemic. Moreover, we collected data about comorbidities such as obesity, hypertension and diabetes putting patients at risk of a severe form of COVID‐19 infection, and information about a clinically confirmed diagnosis of COVID‐19 defined as acute febrile respiratory infection, or sudden onset of headache, myalgia, ageusia, anosmia or asthenia, as well as COVID‐19 confirmation by PCR testing and hospitalization. Overall, data from 1418 patients were included. Patient characteristics are detailed in Table 1. Of the included patients, 300 were receiving methotrexate, 26 cyclosporine, 4 acitretin, 48 apremilast, 25 etanercept, 165 adalimumab, 40 infliximab, 8 certolizumab pegol, 240 ustekinumab, 206 secukinumab, 112 ixekizumab, 38 brodalumab, 146 guselkumab, 25 risankizumab and 35 combination of methotrexate and biologic. In total, 22.4% of patients on systemic therapy and 13.8% on biologics discontinued treatment during the pandemic.
Table 1

Patient characteristics

Overall populationTreatment initiation periodMaintenance treatment period
n % n % n %
141810023016.22118883.78
Sex
Men79756.2913156.9666656.16
Women61943.719943.0452043.84
Missing data202
Treatment
Systemic33023.276226.8426840.18
Biologic100570.8715667.53849127.29
Anti‐TNF23816.78146.0622418.86
Anti‐interleukin76754.0914261.4762552.61
Apremilast483.39104.33383.20
Combination of methotrexate and biologic352.4720.87332.78
Risk factor for severe COVID‐19 infection
Diabetes1117.83125.15998.32
Obesity (BMI> 30)24517.28275.1521818.32
HTA23216.363113.3020116.89
None92064.8816369.9675763.61

Treatment initiation period defined as the 4 months following treatment initiation. Maintenance treatment period defined as starting the 5th month of treatment. Systemic treatment: acitretin, methotrexate, cyclosporine. Anti‐TNF: etanercept, adalimumab, infliximab, certolizumab pegol. Anti‐interleukin: ustekinumab, secukinumab, ixekizumab, brodalumab, guselkumab, risankizumab.

Patient characteristics Treatment initiation period defined as the 4 months following treatment initiation. Maintenance treatment period defined as starting the 5th month of treatment. Systemic treatment: acitretin, methotrexate, cyclosporine. Anti‐TNF: etanercept, adalimumab, infliximab, certolizumab pegol. Anti‐interleukin: ustekinumab, secukinumab, ixekizumab, brodalumab, guselkumab, risankizumab. We reported five patients with COVID‐19 infection requiring hospitalization: a 27‐year‐old obese woman with Crohn’s disease treated with adalimumab, a 36‐year‐old man treated with guselkumab, a 53‐year‐old man treated with methotrexate, and two patients required intensive care: a 71‐year‐old obese woman treated with methotrexate and etanercept, a 34‐year‐old obese man treated with ustekinumab. No deaths were reported. In all, 54 patients presented with a possible COVID‐19 infection; confirmation by PCR testing was performed for 12 patients. The frequency of cases according to treatment and treatment period is specified in Table 2.
Table 2

Frequency of COVID‐19 infection cases according to treatment and treatment period

Overall populationTreatment initiation periodMaintenance treatment period
n % n % n %
Overall population
Probable case543.8162.58484.04
Case confirmed by PCR120.8510.43110.93
Case confirmed by PCR and hospitalized50.3510.4340.34
Systemic treatments
Probable case175.1523.17155.60
Case confirmed by PCR30.9100.0031.12
Case confirmed by PCR and hospitalized10.3000.0010.37
Biologics
Probable case333.2831.92303.53
Case confirmed by PCR80.8010.6470.82
Case confirmed by PCR and hospitalized30.3010.6420.24
Apremilast
Probable case36.25110.0025.26
Case confirmed by PCR00.0000.0000.00
Case confirmed by PCR and hospitalized00.0000.0000.00
Combination of methotrexate and biologics
Probable case12.8600.0013.03
Case confirmed by PCR12.8600.0013.03
Case confirmed by PCR and hospitalized12.8600.0013.03

Probable case defined as acute febrile respiratory infection, or sudden onset of headache, myalgia, ageusia, anosmia or asthenia. Treatment initiation period defined as 4 months following treatment initiation. Maintenance treatment period defined as starting the 5th month of treatment. PCR: polymerase chain reaction.

Frequency of COVID‐19 infection cases according to treatment and treatment period Probable case defined as acute febrile respiratory infection, or sudden onset of headache, myalgia, ageusia, anosmia or asthenia. Treatment initiation period defined as 4 months following treatment initiation. Maintenance treatment period defined as starting the 5th month of treatment. PCR: polymerase chain reaction. In our study, 0.35% of patients had a severe form of COVID‐19 requiring hospitalization, 60% of whom (all in intensive care units) presented with other risk factors for severe infection. Two patients were hospitalized, due to their SBT, considered at the beginning of the pandemic as a risk factor for a severe form of COVID‐19 infection. Our data are consistent with those collected and analysed in Italy: Damiani et al. reported 5 hospitalizations out of 1193 patients treated by biologic or small molecules for their psoriasis, and no death was reported. Gisondi et al. reported in Northern Italy 4 hospitalizations out of 5206 patients receiving biologic treatment for psoriasis, again no death was reported. There was no over‐risk of hospitalization in intensive care and death reported for patients receiving biological psoriasis treatment when compared to the general population. Moreover, biologic treatment using immunosuppressive drugs such as guselkumab, ustekinumab, adalimumab, secukinumab, brodalumab or ixekizumab may even protect against the onset and evolution of COVID‐19 infection. , , [Correction added on 28 August 2020, after first online publication: On paragraph 8, the word ‘brodalumab’ has been added in this version.] We did not observe a significant difference in the number severe cases of COVID‐19, according to whether the patient was in the treatment initiation period (1 out of 230 patients) or in the maintenance period (4 out of 1188 patients), Fisher test P = 0.58, OR = 1.29 [95%CI 0.03–13.4]. The absence of a control group and no PCR or serologic confirmations of all probable cases were limitations of this study. In conclusion, our study provides first data showing that there is no increased incidence of severe COVID‐19 in psoriasis patients receiving SBT in the treatment initiation period compared to those in the maintenance period. Results may allow physicians to initiate, on a case‐by‐case basis, SBT in patients with severe psoriasis in the context of COVID‐19 pandemic.

Conflict of interest

None.

Funding sources

None.
  6 in total

1.  Risk of Serious Infection With Biologic and Systemic Treatment of Psoriasis: Results From the Psoriasis Longitudinal Assessment and Registry (PSOLAR).

Authors:  Robert E Kalb; David F Fiorentino; Mark G Lebwohl; John Toole; Yves Poulin; Arnon D Cohen; Kavitha Goyal; Steven Fakharzadeh; Stephen Calabro; Marc Chevrier; Wayne Langholff; Yin You; Craig L Leonardi
Journal:  JAMA Dermatol       Date:  2015-09       Impact factor: 10.282

2.  Biologics increase the risk of SARS-CoV-2 infection and hospitalization, but not ICU admission and death: Real-life data from a large cohort during red-zone declaration.

Authors:  Giovanni Damiani; Alessia Pacifico; Nicola L Bragazzi; Piergiorgio Malagoli
Journal:  Dermatol Ther       Date:  2020-05-19       Impact factor: 2.851

3.  Evolution of COVID-19 infection in four psoriatic patients treated with biological drugs.

Authors:  A Conti; C Lasagni; L Bigi; G Pellacani
Journal:  J Eur Acad Dermatol Venereol       Date:  2020-06-08       Impact factor: 9.228

4.  The impact of the COVID-19 pandemic on patients with chronic plaque psoriasis being treated with biological therapy: the Northern Italy experience.

Authors:  P Gisondi; P Facheris; P Dapavo; S Piaserico; A Conti; L Naldi; S Cazzaniga; P Malagoli; A Costanzo
Journal:  Br J Dermatol       Date:  2020-05-28       Impact factor: 11.113

5.  SARS-CoV-2 infection in a psoriatic patient treated with IL-17 inhibitor.

Authors:  R Balestri; G Rech; C R Girardelli
Journal:  J Eur Acad Dermatol Venereol       Date:  2020-06-08       Impact factor: 9.228

6.  Improvement of SARS-CoV-2 symptoms following Guselkumab injection in a psoriatic patient.

Authors:  F Benhadou; V Del Marmol
Journal:  J Eur Acad Dermatol Venereol       Date:  2020-06-04       Impact factor: 9.228

  6 in total
  15 in total

1.  A survey of psoriasis patients on biologics during COVID-19: a high-epidemic area experience - Franche Comté, France.

Authors:  Irène Gallais-Serezal; Eve Puzenat; Joséphine Moreau; Flora Dresco; Fabien Pelletier; Charlée Nardin; François Aubin
Journal:  Eur J Dermatol       Date:  2021-02-01       Impact factor: 3.328

Review 2. 

Authors:  Stephan Grabbe; Stefan Beissert; Alexander Enk
Journal:  J Dtsch Dermatol Ges       Date:  2020-08       Impact factor: 5.584

3.  Use of Methotrexate in the Treatment of Moderate to Severe Plaque Psoriasis in France: A Practice Survey.

Authors:  Anne-Claire Fougerousse; Laure Mery-Bossard; Josiane Parier; Charles Taieb; Antoine Bertolotti; Francois Maccari
Journal:  Clin Cosmet Investig Dermatol       Date:  2021-04-23

4.  Furin Expression in Patients With Psoriasis-A Patient Cohort Endangered to SARS-COV2?

Authors:  Thomas Graier; Nicole Golob-Schwarzl; Wolfgang Weger; Theresa Benezeder; Clemens Painsi; Wolfgang Salmhofer; Peter Wolf
Journal:  Front Med (Lausanne)       Date:  2021-02-10

5.  COVID-19 patients with psoriasis and psoriatic arthritis on biologic immunosuppressant therapy vs apremilast in North Spain.

Authors:  Rubén Queiro Silva; Susana Armesto; Carmen González Vela; Cristina Naharro Fernández; Miguel Angel González-Gay
Journal:  Dermatol Ther       Date:  2020-07-27       Impact factor: 3.858

6.  COVID-19 and immune-mediated inflammatory diseases: Why don't our patients get worse?

Authors:  Víctor M Martínez-Taboada; Marcos López-Hoyos; Javier Crespo; José L Hernández
Journal:  Autoimmun Rev       Date:  2020-10-27       Impact factor: 9.754

Review 7.  Biologics for Psoriasis during the COVID-19 Pandemic.

Authors:  Koji Kamiya; Mayumi Komine; Mamitaro Ohtsuki
Journal:  J Clin Med       Date:  2021-03-30       Impact factor: 4.241

8.  Concerns related to the coronavirus disease 2019 pandemic in adult patients with atopic dermatitis and psoriasis treated with systemic immunomodulatory therapy: a Danish questionnaire survey.

Authors:  N D Loft; A-S Halling; L Iversen; C Vestergaard; M Deleuran; M K Rasmussen; C Zachariae; J P Thyssen; L Skov
Journal:  J Eur Acad Dermatol Venereol       Date:  2020-09-17       Impact factor: 9.228

Review 9.  Systemic immunosuppression in times of COVID-19: Do we need to rethink our standards?

Authors:  Stephan Grabbe; Stefan Beissert; Alexander Enk
Journal:  J Dtsch Dermatol Ges       Date:  2020-08-02       Impact factor: 5.231

10.  National Psoriasis Foundation COVID-19 Task Force Guidance for Management of Psoriatic Disease During the Pandemic: Version 1.

Authors:  Joel M Gelfand; April W Armstrong; Stacie Bell; George L Anesi; Andrew Blauvelt; Cassandra Calabrese; Erica D Dommasch; Steve R Feldman; Dafna Gladman; Leon Kircik; Mark Lebwohl; Vincent Lo Re; George Martin; Joseph F Merola; Jose U Scher; Sergio Schwartzman; James R Treat; Abby S Van Voorhees; Christoph T Ellebrecht; Justine Fenner; Anthony Ocon; Maha N Syed; Erica J Weinstein; Jessica Smith; George Gondo; Sue Heydon; Samantha Koons; Christopher T Ritchlin
Journal:  J Am Acad Dermatol       Date:  2020-09-04       Impact factor: 15.487

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.