Use of Systemic Therapies for Treatment of Psoriasis in People Living with Controlled HIV: Inference-Based Guidance from a Multidisciplinary Expert Panel.

Evidence-based dermatology HIV Human immunodeficiency virus Immunodeficiency Immunosuppression Immunotherapy Medical education Psoriasis

Journal

Dermatology and therapy
ISSN: 2193-8210
Titre abrégé: Dermatol Ther (Heidelb)
Pays: Switzerland
ID NLM: 101590450

Informations de publication

Date de publication:
May 2022
Historique:
received: 04 03 2022
accepted: 30 03 2022
pubmed: 22 4 2022
medline: 22 4 2022
entrez: 21 4 2022
Statut: ppublish

Résumé

People living with human immunodeficiency virus (PLHIV) have a similar prevalence of psoriasis as the general population, though incidence and severity correlate with HIV viral load. Adequately treating HIV early renders the infection a chronic medical condition and allows PLHIV with a suppressed viral load (PLHIV-s) to live normal lives. Despite this, safety concerns and a lack of high-level data have hindered the use of systemic psoriasis therapies in PLHIV-s. We aim to provide a structured framework that supports healthcare professionals and patients discussing the risks and benefits of systemic psoriasis therapy in PLHIV-s. Our goal was to address the primary question, are responses to systemic therapies for the treatment of psoriasis in PLHIV-s similar to those in the non-HIV population? We implemented an inference-based approach relying on indirect evidence when direct clinical trial data were absent. In this instance, we reviewed indirect evidence supporting inferences on the status of immune function in PLHIV. Recommendations on systemic treatment for psoriasis in PLHIV were derived using an inferential heuristic. We identified seven indirect indicators of immune function informed by largely independent bodies of evidence: (1) functional assays, (2) vaccine response, (3) life expectancy, (4) psoriasis manifestations, (5) rate of infections, (6) rate of malignancies, and (7) organ transplant outcomes. Drug-related benefits and risks when treating a patient with systemic psoriasis therapies are similar for non-HIV patients and PLHIV with a suppressed viral load and normalized CD4 counts. Prior to initiating psoriasis treatment in PLHIV, HIV replication should be addressed by an HIV specialist. Exercise additional caution for patients with a suppressed viral load and discordant CD4 responses on antiretroviral therapy. People living with human immunodeficiency virus (PLHIV) develop psoriasis as often as everyone else. We asked: what are effective and safe treatments when PLHIV need systemic therapy (pills or injections) for their psoriasis?HIV infection attacks the immune system. When HIV is not treated, the immune system declines. A less effective immune system makes it harder for the body to fight infections and certain cancers. Psoriasis is a skin condition caused by overactive immune cells. Effective psoriasis treatments reduce immune-cell activity. There are some concerns that treatments for psoriasis may not work and could worsen infections or cancers.To answer the question, we gathered 11 dermatologists and 4 HIV specialists. We reviewed the international scientific literature on PLHIV and psoriasis. The absence of direct evidence and volume of information to review made the process challenging. The end results were worthwhile.We concluded that people who are diagnosed early and take antiretroviral therapy to control their HIV infection (PLHIV-c) can live long, healthy lives. Accordingly, we determined that PLHIV-c can likely expect the same safety and efficacy for systemic psoriasis treatments as the general population. Treatment decisions should be made on a case-by-case basis through consultation with the patient and treating physician(s).Pillars of modern medicine are evidence-based care and collaborative decision-making. Too often, neither care provider nor patient are adequately informed. We have tried to fill one information gap for PLHIV and psoriasis. This process may help answer questions in other disease populations where direct evidence is scarce or absent.

Sections du résumé

BACKGROUND BACKGROUND
People living with human immunodeficiency virus (PLHIV) have a similar prevalence of psoriasis as the general population, though incidence and severity correlate with HIV viral load. Adequately treating HIV early renders the infection a chronic medical condition and allows PLHIV with a suppressed viral load (PLHIV-s) to live normal lives. Despite this, safety concerns and a lack of high-level data have hindered the use of systemic psoriasis therapies in PLHIV-s.
OBJECTIVES OBJECTIVE
We aim to provide a structured framework that supports healthcare professionals and patients discussing the risks and benefits of systemic psoriasis therapy in PLHIV-s. Our goal was to address the primary question, are responses to systemic therapies for the treatment of psoriasis in PLHIV-s similar to those in the non-HIV population?
METHODS METHODS
We implemented an inference-based approach relying on indirect evidence when direct clinical trial data were absent. In this instance, we reviewed indirect evidence supporting inferences on the status of immune function in PLHIV. Recommendations on systemic treatment for psoriasis in PLHIV were derived using an inferential heuristic.
RESULTS RESULTS
We identified seven indirect indicators of immune function informed by largely independent bodies of evidence: (1) functional assays, (2) vaccine response, (3) life expectancy, (4) psoriasis manifestations, (5) rate of infections, (6) rate of malignancies, and (7) organ transplant outcomes.
CONCLUSIONS CONCLUSIONS
Drug-related benefits and risks when treating a patient with systemic psoriasis therapies are similar for non-HIV patients and PLHIV with a suppressed viral load and normalized CD4 counts. Prior to initiating psoriasis treatment in PLHIV, HIV replication should be addressed by an HIV specialist. Exercise additional caution for patients with a suppressed viral load and discordant CD4 responses on antiretroviral therapy.
People living with human immunodeficiency virus (PLHIV) develop psoriasis as often as everyone else. We asked: what are effective and safe treatments when PLHIV need systemic therapy (pills or injections) for their psoriasis?HIV infection attacks the immune system. When HIV is not treated, the immune system declines. A less effective immune system makes it harder for the body to fight infections and certain cancers. Psoriasis is a skin condition caused by overactive immune cells. Effective psoriasis treatments reduce immune-cell activity. There are some concerns that treatments for psoriasis may not work and could worsen infections or cancers.To answer the question, we gathered 11 dermatologists and 4 HIV specialists. We reviewed the international scientific literature on PLHIV and psoriasis. The absence of direct evidence and volume of information to review made the process challenging. The end results were worthwhile.We concluded that people who are diagnosed early and take antiretroviral therapy to control their HIV infection (PLHIV-c) can live long, healthy lives. Accordingly, we determined that PLHIV-c can likely expect the same safety and efficacy for systemic psoriasis treatments as the general population. Treatment decisions should be made on a case-by-case basis through consultation with the patient and treating physician(s).Pillars of modern medicine are evidence-based care and collaborative decision-making. Too often, neither care provider nor patient are adequately informed. We have tried to fill one information gap for PLHIV and psoriasis. This process may help answer questions in other disease populations where direct evidence is scarce or absent.

Autres résumés

Type: plain-language-summary (eng)
People living with human immunodeficiency virus (PLHIV) develop psoriasis as often as everyone else. We asked: what are effective and safe treatments when PLHIV need systemic therapy (pills or injections) for their psoriasis?HIV infection attacks the immune system. When HIV is not treated, the immune system declines. A less effective immune system makes it harder for the body to fight infections and certain cancers. Psoriasis is a skin condition caused by overactive immune cells. Effective psoriasis treatments reduce immune-cell activity. There are some concerns that treatments for psoriasis may not work and could worsen infections or cancers.To answer the question, we gathered 11 dermatologists and 4 HIV specialists. We reviewed the international scientific literature on PLHIV and psoriasis. The absence of direct evidence and volume of information to review made the process challenging. The end results were worthwhile.We concluded that people who are diagnosed early and take antiretroviral therapy to control their HIV infection (PLHIV-c) can live long, healthy lives. Accordingly, we determined that PLHIV-c can likely expect the same safety and efficacy for systemic psoriasis treatments as the general population. Treatment decisions should be made on a case-by-case basis through consultation with the patient and treating physician(s).Pillars of modern medicine are evidence-based care and collaborative decision-making. Too often, neither care provider nor patient are adequately informed. We have tried to fill one information gap for PLHIV and psoriasis. This process may help answer questions in other disease populations where direct evidence is scarce or absent.

Identifiants

pubmed: 35445963
doi: 10.1007/s13555-022-00722-0
pii: 10.1007/s13555-022-00722-0
pmc: PMC9110627
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1073-1089

Subventions

Organisme : AbbVie (CA)
ID : Unrestricted educational grant
Organisme : Amgen Canada
ID : Unrestricted educational grant
Organisme : Janssen Canada
ID : Unrestricted educational grant
Organisme : LEO Pharma (CA)
ID : Unrestricted educational grant
Organisme : Novartis Pharmaceuticals Canada
ID : Unrestricted educational grant
Organisme : SUN Pharmaceuticals (CA)
ID : Unrestricted educational grant

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2022. The Author(s).

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Auteurs

Kim A Papp (KA)

Probity Medical Research Inc., Waterloo, ON, Canada. kapapp@probitymedical.com.
K Papp Clinical Research, Waterloo, ON, Canada. kapapp@probitymedical.com.

Jennifer Beecker (J)

Probity Medical Research Inc., Waterloo, ON, Canada.
University of Ottawa, Ottawa, ON, Canada.
Division of Dermatology, The Ottawa Hospital, Ottawa, ON, Canada.
Ottawa Hospital Research Institute, Ottawa, ON, Canada.

Curtis Cooper (C)

University of Ottawa, Ottawa, ON, Canada.
Ottawa Hospital Research Institute, Ottawa, ON, Canada.
The Ottawa Hospital and Regional Hepatitis Program, Ottawa, ON, Canada.

Mark G Kirchhof (MG)

University of Ottawa, Ottawa, ON, Canada.
Division of Dermatology, The Ottawa Hospital, Ottawa, ON, Canada.

Anton L Pozniak (AL)

Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Juergen K Rockstroh (JK)

Department of Medicine, University of Bonn, Bonn, Germany.

Jan P Dutz (JP)

Skin Care Center, Vancouver, BC, Canada.
Department of Dermatology and Skin Science, University of British Columbia, Vancouver, BC, Canada.
BC Children's Hospital Research Institute, Vancouver, BC, Canada.

Melinda J Gooderham (MJ)

Probity Medical Research Inc., Waterloo, ON, Canada.
SKiN Centre for Dermatology, Peterborough, ON, Canada.

Robert Gniadecki (R)

Division of Dermatology, Department of Medicine, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.

Chih-Ho Hong (CH)

Probity Medical Research Inc., Waterloo, ON, Canada.
Department of Dermatology and Skin Science, University of British Columbia, Vancouver, BC, Canada.
Dr. Chih-Ho Hong Medical Inc., Surrey, BC, Canada.

Charles W Lynde (CW)

Probity Medical Research Inc., Waterloo, ON, Canada.
Lynde Institute for Dermatology, Markham, ON, Canada.

Catherine Maari (C)

Innovaderm Research Inc, Montreal, QC, Canada.

Yves Poulin (Y)

Centre de Recherche Dermatologique du Québec Métropolitain, Quebec, QC, Canada.

Ronald B Vender (RB)

Dermatrials Research Inc., Hamilton, ON, Canada.
Department of Medicine, McMaster University, Hamilton, ON, Canada.

Sharon L Walmsley (SL)

Toronto General Hospital Research Institute, Toronto, ON, Canada.
University of Toronto, Toronto, ON, Canada.
Department of Medicine, University Health Network, Toronto, ON, Canada.

Classifications MeSH