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Drug holiday in patients with polycystic liver disease treated with somatostatin analogues

BACKGROUND: Somatostatin analogues (SAs) reduce liver volume and relief symptoms in polycystic liver disease (PLD). Its effect wears off after continuing therapy suggesting development of SA tolerance in patients on chronic therapy. We postulate that a drug holiday resensitizes the liver to its acut...

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Autores principales: van Aerts, René M. M., Kolkman, Marieke, Kievit, Wietske, Gevers, Tom J. G., Nevens, Frederik, Drenth, Joost P. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6172936/
https://www.ncbi.nlm.nih.gov/pubmed/30302127
http://dx.doi.org/10.1177/1756284818804784
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author van Aerts, René M. M.
Kolkman, Marieke
Kievit, Wietske
Gevers, Tom J. G.
Nevens, Frederik
Drenth, Joost P. H.
author_facet van Aerts, René M. M.
Kolkman, Marieke
Kievit, Wietske
Gevers, Tom J. G.
Nevens, Frederik
Drenth, Joost P. H.
author_sort van Aerts, René M. M.
collection PubMed
description BACKGROUND: Somatostatin analogues (SAs) reduce liver volume and relief symptoms in polycystic liver disease (PLD). Its effect wears off after continuing therapy suggesting development of SA tolerance in patients on chronic therapy. We postulate that a drug holiday resensitizes the liver to its acute pharmacological effects. Therefore, this study examines the liver volume-reducing effect of SAs after a drug holiday. METHODS: Patients were identified from the International PLD Registry and included in our analysis when (1) treated with SAs during two cycles separated by a drug holiday and (2) height-adjusted total liver volume (hTLV) was available at start and end of each cycle. For our primary outcome we compared the effect of SAs (in % per 6 months) on hTLV between the first and second treatment cycle. RESULTS: In 34 patients, initial liver volume-reducing effect was similar to that after rechallenge [−2.6% per 6 months (interquartile range, −3.8–0.8) versus −1.6% per 6 months (interquartile range, −3.1–1.1), p = 0.510]. Cessation of treatment led to a rebound effect, but liver volume remained stable compared with the baseline with intermittent therapy in responders to SA [−0.6% (interquartile range, −7.4–5.7) after 46.5 months]. CONCLUSIONS: PLD patients treated with SAs benefit from retreatment after a drug holiday. The significant increase of liver volume after cessation of treatment complicates widespread use of a drug holiday as new treatment strategy. Our results contribute to a better understanding of the pharmacological effect of SAs and help to identify patients who might benefit.
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spelling pubmed-61729362018-10-09 Drug holiday in patients with polycystic liver disease treated with somatostatin analogues van Aerts, René M. M. Kolkman, Marieke Kievit, Wietske Gevers, Tom J. G. Nevens, Frederik Drenth, Joost P. H. Therap Adv Gastroenterol Original Research BACKGROUND: Somatostatin analogues (SAs) reduce liver volume and relief symptoms in polycystic liver disease (PLD). Its effect wears off after continuing therapy suggesting development of SA tolerance in patients on chronic therapy. We postulate that a drug holiday resensitizes the liver to its acute pharmacological effects. Therefore, this study examines the liver volume-reducing effect of SAs after a drug holiday. METHODS: Patients were identified from the International PLD Registry and included in our analysis when (1) treated with SAs during two cycles separated by a drug holiday and (2) height-adjusted total liver volume (hTLV) was available at start and end of each cycle. For our primary outcome we compared the effect of SAs (in % per 6 months) on hTLV between the first and second treatment cycle. RESULTS: In 34 patients, initial liver volume-reducing effect was similar to that after rechallenge [−2.6% per 6 months (interquartile range, −3.8–0.8) versus −1.6% per 6 months (interquartile range, −3.1–1.1), p = 0.510]. Cessation of treatment led to a rebound effect, but liver volume remained stable compared with the baseline with intermittent therapy in responders to SA [−0.6% (interquartile range, −7.4–5.7) after 46.5 months]. CONCLUSIONS: PLD patients treated with SAs benefit from retreatment after a drug holiday. The significant increase of liver volume after cessation of treatment complicates widespread use of a drug holiday as new treatment strategy. Our results contribute to a better understanding of the pharmacological effect of SAs and help to identify patients who might benefit. SAGE Publications 2018-10-03 /pmc/articles/PMC6172936/ /pubmed/30302127 http://dx.doi.org/10.1177/1756284818804784 Text en © The Author(s), 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
van Aerts, René M. M.
Kolkman, Marieke
Kievit, Wietske
Gevers, Tom J. G.
Nevens, Frederik
Drenth, Joost P. H.
Drug holiday in patients with polycystic liver disease treated with somatostatin analogues
title Drug holiday in patients with polycystic liver disease treated with somatostatin analogues
title_full Drug holiday in patients with polycystic liver disease treated with somatostatin analogues
title_fullStr Drug holiday in patients with polycystic liver disease treated with somatostatin analogues
title_full_unstemmed Drug holiday in patients with polycystic liver disease treated with somatostatin analogues
title_short Drug holiday in patients with polycystic liver disease treated with somatostatin analogues
title_sort drug holiday in patients with polycystic liver disease treated with somatostatin analogues
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6172936/
https://www.ncbi.nlm.nih.gov/pubmed/30302127
http://dx.doi.org/10.1177/1756284818804784
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