The "Personalising Actinic Keratosis Treatment for Immunocompromised Patients" (IM-PAKT) Project: An Expert Panel Opinion
- PMID: 38902589
- PMCID: PMC11264500
- DOI: 10.1007/s13555-024-01215-y
The "Personalising Actinic Keratosis Treatment for Immunocompromised Patients" (IM-PAKT) Project: An Expert Panel Opinion
Abstract
Actinic keratosis (AK) is an intraepithelial condition characterized by the development of scaly, erythematous lesions after repeated exposure to ultraviolet radiation. Significant immunosuppression is a risk factor for the development of AK and subsequent lesion progression to squamous cell carcinoma. Immunocompromised patients (ICPs), particularly organ transplant recipients, often have more advanced or complex AK presentations and an increased risk of skin carcinomas versus non-ICPs with AK, making lesions more difficult to treat and resulting in worse treatment outcomes. The recent "Personalising Actinic Keratosis Treatment" (PAKT) consensus reported that delivering patient-centric care may play a role in supporting better clinical outcomes and patient satisfaction with treatments for chronic dermatologic conditions such as AK, which require repeated cycles of treatment. Additionally, currently published guidance and recommendations were considered by the PAKT panel to be overly broad for managing ICPs with their unique and complex needs. Therefore, the "Personalising Actinic Keratosis Treatment for Immunocompromised Patients" (IM-PAKT) panel was established to build upon general recommendations from the PAKT consensus. The panel identified current gaps in guidance for AK care in ICPs, offered practical care approaches based on typical ICP scenarios, and highlighted the need to adapt AK management to optimize care and improve treatment outcomes in ICPs. In particular, dermatologists should establish collaborative and transparent relationships with patients' multidisciplinary teams to enhance overall care for patients' comorbidities: given their increased risk of progression to malignancy, earlier assessments/interventions and frequent follow-ups are vital.The panel also developed a novel "triage" tool outlining effective treatment follow-up and disease surveillance plans tailored to patients' risk profiles, guided by current clinical presentation and relevant medical history. Additionally, we present the panel's expert opinion on three fictional ICP scenarios to explain their decision-making process for assessing and managing typical ICPs that they may encounter in clinical practice.
Keywords: Actinic keratosis; Expert testimony; Immunocompromised host; Organ transplantation; Treatment outcomes.
© 2024. The Author(s).
Conflict of interest statement
Rolf Markus Szeimies has received grants from Almirall, Biofrontera, Dr. Wolff-Group, Galderma, Leo Pharma, Novartis, and Photonamic for clinical studies, has received consulting fees and speaker honoraria from Abbvie, Almirall, Eli Lilly, Galderma, Janssen, and Leo Pharma, and is Vice-President of the EURO-PDT Society. Claas Ulrich has received study grants and/or has served as speaker and advisor for AlphaTau, Almirall, Beiersdorf, BMS, Galderma, GME, Hans Karrer AG, Novartis, Philogen, Pierre Fabre, Regeneron, Sanofi, Sun Pharma. Carla Ferrándiz-Pulido declares to have participated in advisory boards and/or received honoraria from Almirall, Pierre Fabre, Sanofi, and Sun Pharma. Gunther Hofbauer has received research support from the Swiss National Fund, has acted as a speaker for AbbVie, Galderma Spirig, LEO Pharma, L’Oréal, Louis Widmer, MEDA, Merck, Novartis, Permamed, Pfizer, Pierre Fabre, Sanofi Genzyme, and acted as a consultant for AbbVie, Almirall, Biofrontera/Louis Widmer, Galderma Spirig, Hoffmann-La Roche, LEO Pharma, MEDA, Novartis, Sanofi Genzyme. John Thomas Lear has acted as an advisor and received honoraria from Almirall, Galderma, and Leo Pharma. Celeste Lebbé has served as a consultant for Bristol Myers Squibb, Galderma, Immunocore, MSD, Novartis, and Pierre Fabre. Stefano Piaserico has no conflicts of interest relating to the publication of this manuscript. Merete Hædersdal has received research grants from or acted as a consultant for Galderma, Leo Pharma, L’Oréal/La Roche-Posay, Lutronic, Procter & Gamble, and Venus Concept, has acted as a lecturer for Galderma, and has received equipment from Cherry Imaging, Cynosure, GME Medical, Lutronic, MiraDry, and Venus Concept.
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