Sustained Regression of Hydroxycarbamide Induced Actinic Keratoses after Switching to Anagrelide

Hydroxycarbamide (HC) is the first-line treatment for certain myeloproliferative neoplasms, such as polycythemia vera and essential thrombocytosis (ET). In a subset of these patients long-term treatment with HC can result in the development of confluent actinic keratoses (AK) followed by invasive ke...

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Main Authors: Georgios Gaitanis, Dora Gougopoulou, Eleni Kapsali, Ioannis D. Bassukas
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Case Reports in Dermatological Medicine
Online Access:http://dx.doi.org/10.1155/2018/2874012
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author Georgios Gaitanis
Dora Gougopoulou
Eleni Kapsali
Ioannis D. Bassukas
author_facet Georgios Gaitanis
Dora Gougopoulou
Eleni Kapsali
Ioannis D. Bassukas
author_sort Georgios Gaitanis
collection DOAJ
description Hydroxycarbamide (HC) is the first-line treatment for certain myeloproliferative neoplasms, such as polycythemia vera and essential thrombocytosis (ET). In a subset of these patients long-term treatment with HC can result in the development of confluent actinic keratoses (AK) followed by invasive keratinocytic carcinomas (“squamous dysplasia”), preferentially on sun-exposed skin. Discontinuation or dose reduction of HC may result in partial improvement. A 59-year-old farmer after 14 years on HC (2 gr/d) and acetylsalicylic acid (100 mg/d) for ET, was referred for numerous, hyperkeratotic AK on face, scalp, and hands that could not be controlled with repeated (N=15) cryosurgery sessions in the previous 3 years. Acitretin (0.32 mg/kg daily) and topical treatments (cryosurgery with ingenol mebutate) were initiated with only marginal improvement after 3 months. Acitretin dose was doubled and HC was switched to anagrelide (0.5 mg twice daily). Within a month the AK load regressed significantly and, at 3 months follow-up, complete clinical remission was achieved and acitretin was discontinued. Twenty months later the patient is clear from AK. In conclusion, the impressive and sustainable AK remission under anagrelide draws attention to a possible role of the phosphodiesterase 3 pathway, the major pharmacological target of anagrelide, as a potential therapeutic target for keratinocytic cancers.
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spelling doaj-art-7ce3d8a719d641b8ac33c41873f21c942025-02-03T05:53:50ZengWileyCase Reports in Dermatological Medicine2090-64632090-64712018-01-01201810.1155/2018/28740122874012Sustained Regression of Hydroxycarbamide Induced Actinic Keratoses after Switching to AnagrelideGeorgios Gaitanis0Dora Gougopoulou1Eleni Kapsali2Ioannis D. Bassukas3Department of Skin and Venereal Diseases, Faculty of Medicine, School of Health Sciences, University of Ioannina, Ioannina, GreeceHematology Clinic, Department of Internal Medicine, Faculty of Medicine, School of Health Sciences, University of Ioannina, Ioannina, GreeceHematology Clinic, Department of Internal Medicine, Faculty of Medicine, School of Health Sciences, University of Ioannina, Ioannina, GreeceDepartment of Skin and Venereal Diseases, Faculty of Medicine, School of Health Sciences, University of Ioannina, Ioannina, GreeceHydroxycarbamide (HC) is the first-line treatment for certain myeloproliferative neoplasms, such as polycythemia vera and essential thrombocytosis (ET). In a subset of these patients long-term treatment with HC can result in the development of confluent actinic keratoses (AK) followed by invasive keratinocytic carcinomas (“squamous dysplasia”), preferentially on sun-exposed skin. Discontinuation or dose reduction of HC may result in partial improvement. A 59-year-old farmer after 14 years on HC (2 gr/d) and acetylsalicylic acid (100 mg/d) for ET, was referred for numerous, hyperkeratotic AK on face, scalp, and hands that could not be controlled with repeated (N=15) cryosurgery sessions in the previous 3 years. Acitretin (0.32 mg/kg daily) and topical treatments (cryosurgery with ingenol mebutate) were initiated with only marginal improvement after 3 months. Acitretin dose was doubled and HC was switched to anagrelide (0.5 mg twice daily). Within a month the AK load regressed significantly and, at 3 months follow-up, complete clinical remission was achieved and acitretin was discontinued. Twenty months later the patient is clear from AK. In conclusion, the impressive and sustainable AK remission under anagrelide draws attention to a possible role of the phosphodiesterase 3 pathway, the major pharmacological target of anagrelide, as a potential therapeutic target for keratinocytic cancers.http://dx.doi.org/10.1155/2018/2874012
spellingShingle Georgios Gaitanis
Dora Gougopoulou
Eleni Kapsali
Ioannis D. Bassukas
Sustained Regression of Hydroxycarbamide Induced Actinic Keratoses after Switching to Anagrelide
Case Reports in Dermatological Medicine
title Sustained Regression of Hydroxycarbamide Induced Actinic Keratoses after Switching to Anagrelide
title_full Sustained Regression of Hydroxycarbamide Induced Actinic Keratoses after Switching to Anagrelide
title_fullStr Sustained Regression of Hydroxycarbamide Induced Actinic Keratoses after Switching to Anagrelide
title_full_unstemmed Sustained Regression of Hydroxycarbamide Induced Actinic Keratoses after Switching to Anagrelide
title_short Sustained Regression of Hydroxycarbamide Induced Actinic Keratoses after Switching to Anagrelide
title_sort sustained regression of hydroxycarbamide induced actinic keratoses after switching to anagrelide
url http://dx.doi.org/10.1155/2018/2874012
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AT elenikapsali sustainedregressionofhydroxycarbamideinducedactinickeratosesafterswitchingtoanagrelide
AT ioannisdbassukas sustainedregressionofhydroxycarbamideinducedactinickeratosesafterswitchingtoanagrelide