Literature DB >> 29235161

Management of actinic keratosis at specific body sites in patients at high risk of carcinoma lesions: expert consensus from the AKTeam™ of expert clinicians.

M A Richard1, J M Amici2,3, N Basset-Seguin4, J P Claudel5,6, B Cribier7, B Dreno8.   

Abstract

Actinic keratoses (AK) arise on sun-exposed regions of the skin. If left untreated, AK may progress to invasive squamous cell carcinoma (SCC), although the rate of progression is low. A practical treatment algorithm for the treatment of AK in standard situations has been published by the AKTeam™ expert panel. However, management of particular situations of AK with increasing/higher carcinoma risk or AK progressing into carcinomas with increased aggressiveness due to their anatomical location (risky areas), or in patients with an increased risk of SCC requires further discussion. These include AK on the dorsal hands, forearms, legs, periorbital region, eyelids, ears, or lips, and organ transplant recipients, patients undergoing treatment with carcinogenic agents and patients with chronic lymphocytic leukaemia. The main objective was to propose therapeutic strategies for the treatment of AK located in risky areas and in patients with more invasive/aggressive lesions and a higher risk of progression to SCC. A systematic review of the literature was initially performed, and results were discussed by the experts to propose best management practices in specific situations. Finally, adapted management strategies for AK occurring in risky areas and in high-risk patients are presented, taking into account the experts' own clinical experience and current guidelines. In most of these 'at-risk' situations, patients can be treated according to the AKTeam™ treatment algorithm. Difficult-to-treat lesions should be treated more aggressively due to their higher risk of transformation. For patients with skin that is highly susceptible to actinic damage, monitoring and sun protection strategies are mandatory, and patients should undergo more regular follow-up. Further assessment of newer therapies in clinical trials is necessary to determine optimal treatment conditions. This expert consensus provides guidance for the management of AK in risky body sites and in patients with an increasing/higher risk for SCCs.
© 2017 European Academy of Dermatology and Venereology.

Entities:  

Mesh:

Year:  2018        PMID: 29235161     DOI: 10.1111/jdv.14753

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN: 0926-9959            Impact factor:   6.166


  5 in total

1.  A Single-Arm, Open-Label, Phase IV Study to Evaluate the Efficacy of a Topical Formulation for Hyperkeratotic Actinic Keratosis Lesions.

Authors:  Maria Pia De Padova; Barbara Marzani; Daniela Pinto; Fabio Rinaldi
Journal:  Dermatol Ther (Heidelb)       Date:  2018-07-27

2.  Evaluation of modified Interferon alpha mRNA constructs for the treatment of non-melanoma skin cancer.

Authors:  Sarah Hochmann; Michaela Mittermeir; Radmila Santic; Frieder Koszik; Lanay Griessner; Alina Sarah Sonderegger; Thomas Hoffmann; Elisabeth Russe; Sandra Scheiblhofer; Richard Weiss; Markus Mandler; Achim Schneeberger; Dirk Strunk
Journal:  Sci Rep       Date:  2018-08-28       Impact factor: 4.379

3.  Predicting keratinocyte carcinoma in patients with actinic keratosis: development and internal validation of a multivariable risk-prediction model.

Authors:  S Tokez; M Alblas; T Nijsten; L M Pardo; M Wakkee
Journal:  Br J Dermatol       Date:  2020-02-26       Impact factor: 9.302

4.  Comparison of Actinic Keratosis and Severity Index with Physician Global Assessment and Total Lesion Count and the Ability to Predict Skin Cancer.

Authors:  Ayda Acar; Isil Karaarslan
Journal:  Dermatol Pract Concept       Date:  2022-01-01

5.  Topical Treatment of Actinic Keratosis and Metalloproteinase Expression: A Clinico-Pathological Retrospective Study.

Authors:  Elena Campione; Monia Di Prete; Cosimo Di Raimondo; Gaetana Costanza; Vincenzo Palumbo; Virginia Garofalo; Sara Mazzilli; Chiara Franceschini; Emi Dika; Luca Bianchi; Augusto Orlandi
Journal:  Int J Mol Sci       Date:  2022-09-26       Impact factor: 6.208

  5 in total

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