Cargando…
Safety and tolerability of dienogest in endometriosis: pooled analysis from the European clinical study program
BACKGROUND: In four randomized, controlled, European trials, dienogest 2 mg once daily demonstrated significant efficacy for lesion reduction and reduction in pain intensity in endometriosis. We describe a pooled analysis of the safety and tolerability data from these trials to confirm and further c...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403681/ https://www.ncbi.nlm.nih.gov/pubmed/25926759 http://dx.doi.org/10.2147/IJWH.S77202 |
_version_ | 1782367363208839168 |
---|---|
author | Strowitzki, Thomas Faustmann, Thomas Gerlinger, Christoph Schumacher, Ulrike Ahlers, Christiane Seitz, Christian |
author_facet | Strowitzki, Thomas Faustmann, Thomas Gerlinger, Christoph Schumacher, Ulrike Ahlers, Christiane Seitz, Christian |
author_sort | Strowitzki, Thomas |
collection | PubMed |
description | BACKGROUND: In four randomized, controlled, European trials, dienogest 2 mg once daily demonstrated significant efficacy for lesion reduction and reduction in pain intensity in endometriosis. We describe a pooled analysis of the safety and tolerability data from these trials to confirm and further characterize the safety profile of dienogest in the treatment of endometriosis. METHODS: All 332 women treated with dienogest 2 mg who participated in the four clinical trials were included in the pooled analyses for safety assessments, including adverse events, laboratory tests, vital signs, body weight, and bleeding patterns. Safety variables were analyzed using descriptive statistics. RESULTS: Pooled analyses of this large patient population confirmed that dienogest 2 mg is well tolerated, with a favorable safety profile extending over a period up to 65 weeks in women with endometriosis. The most common adverse drug reactions were headache, breast discomfort, depressed mood, and acne, each occurring in <10% of women. All these adverse events were generally of mild-to-moderate intensity and associated with low discontinuation rates. The bleeding pattern associated with dienogest 2 mg was well tolerated, and only two women (0.6%) reported bleeding events as the primary reason for premature discontinuation. Laboratory and vital sign assessments indicated no safety concerns for dienogest. Estradiol levels were maintained within the low-physiological range, in support of previous evidence indicating that dienogest 2 mg demonstrates therapeutic efficacy without inducing estradiol deficiency. CONCLUSION: In this pooled analysis of 332 women with endometriosis, dienogest was well tolerated with a favorable safety profile extending over a period of up to 65 weeks. There is a paucity of randomized trial evidence to support the use of many treatments in endometriosis. These pooled analyses from four clinical trials of dienogest 2 mg represent a contribution to evidence-based medicine in endometriosis, providing outcomes of potential relevance to daily practice. |
format | Online Article Text |
id | pubmed-4403681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44036812015-04-29 Safety and tolerability of dienogest in endometriosis: pooled analysis from the European clinical study program Strowitzki, Thomas Faustmann, Thomas Gerlinger, Christoph Schumacher, Ulrike Ahlers, Christiane Seitz, Christian Int J Womens Health Original Research BACKGROUND: In four randomized, controlled, European trials, dienogest 2 mg once daily demonstrated significant efficacy for lesion reduction and reduction in pain intensity in endometriosis. We describe a pooled analysis of the safety and tolerability data from these trials to confirm and further characterize the safety profile of dienogest in the treatment of endometriosis. METHODS: All 332 women treated with dienogest 2 mg who participated in the four clinical trials were included in the pooled analyses for safety assessments, including adverse events, laboratory tests, vital signs, body weight, and bleeding patterns. Safety variables were analyzed using descriptive statistics. RESULTS: Pooled analyses of this large patient population confirmed that dienogest 2 mg is well tolerated, with a favorable safety profile extending over a period up to 65 weeks in women with endometriosis. The most common adverse drug reactions were headache, breast discomfort, depressed mood, and acne, each occurring in <10% of women. All these adverse events were generally of mild-to-moderate intensity and associated with low discontinuation rates. The bleeding pattern associated with dienogest 2 mg was well tolerated, and only two women (0.6%) reported bleeding events as the primary reason for premature discontinuation. Laboratory and vital sign assessments indicated no safety concerns for dienogest. Estradiol levels were maintained within the low-physiological range, in support of previous evidence indicating that dienogest 2 mg demonstrates therapeutic efficacy without inducing estradiol deficiency. CONCLUSION: In this pooled analysis of 332 women with endometriosis, dienogest was well tolerated with a favorable safety profile extending over a period of up to 65 weeks. There is a paucity of randomized trial evidence to support the use of many treatments in endometriosis. These pooled analyses from four clinical trials of dienogest 2 mg represent a contribution to evidence-based medicine in endometriosis, providing outcomes of potential relevance to daily practice. Dove Medical Press 2015-04-15 /pmc/articles/PMC4403681/ /pubmed/25926759 http://dx.doi.org/10.2147/IJWH.S77202 Text en © 2015 Strowitzki et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Strowitzki, Thomas Faustmann, Thomas Gerlinger, Christoph Schumacher, Ulrike Ahlers, Christiane Seitz, Christian Safety and tolerability of dienogest in endometriosis: pooled analysis from the European clinical study program |
title | Safety and tolerability of dienogest in endometriosis: pooled analysis from the European clinical study program |
title_full | Safety and tolerability of dienogest in endometriosis: pooled analysis from the European clinical study program |
title_fullStr | Safety and tolerability of dienogest in endometriosis: pooled analysis from the European clinical study program |
title_full_unstemmed | Safety and tolerability of dienogest in endometriosis: pooled analysis from the European clinical study program |
title_short | Safety and tolerability of dienogest in endometriosis: pooled analysis from the European clinical study program |
title_sort | safety and tolerability of dienogest in endometriosis: pooled analysis from the european clinical study program |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403681/ https://www.ncbi.nlm.nih.gov/pubmed/25926759 http://dx.doi.org/10.2147/IJWH.S77202 |
work_keys_str_mv | AT strowitzkithomas safetyandtolerabilityofdienogestinendometriosispooledanalysisfromtheeuropeanclinicalstudyprogram AT faustmannthomas safetyandtolerabilityofdienogestinendometriosispooledanalysisfromtheeuropeanclinicalstudyprogram AT gerlingerchristoph safetyandtolerabilityofdienogestinendometriosispooledanalysisfromtheeuropeanclinicalstudyprogram AT schumacherulrike safetyandtolerabilityofdienogestinendometriosispooledanalysisfromtheeuropeanclinicalstudyprogram AT ahlerschristiane safetyandtolerabilityofdienogestinendometriosispooledanalysisfromtheeuropeanclinicalstudyprogram AT seitzchristian safetyandtolerabilityofdienogestinendometriosispooledanalysisfromtheeuropeanclinicalstudyprogram |