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Effects of treatment interruption due to patient convenience on treatment of once a week teriparatide

OBJECTIVES: Once-weekly teriparatide (W-TPTD) is an effective drug for patients with osteoporosis; however, some patients discontinue W-TPTD owing to its adverse drug reactions (ADRs). Sequential treatment with W-TPTD and antiresorptive therapy may be effective in treating such patients. In this stu...

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Autores principales: Katahira, Genichiro, Akiba, Kotaro, Takada, Junichi, Iba, Kousuke, Yamashita, Toshihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Osteoporosis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093683/
https://www.ncbi.nlm.nih.gov/pubmed/32226827
http://dx.doi.org/10.1016/j.afos.2020.01.001
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author Katahira, Genichiro
Akiba, Kotaro
Takada, Junichi
Iba, Kousuke
Yamashita, Toshihiko
author_facet Katahira, Genichiro
Akiba, Kotaro
Takada, Junichi
Iba, Kousuke
Yamashita, Toshihiko
author_sort Katahira, Genichiro
collection PubMed
description OBJECTIVES: Once-weekly teriparatide (W-TPTD) is an effective drug for patients with osteoporosis; however, some patients discontinue W-TPTD owing to its adverse drug reactions (ADRs). Sequential treatment with W-TPTD and antiresorptive therapy may be effective in treating such patients. In this study, we evaluate the efficacy of this sequential treatment regimen. METHODS: This retrospective study was conducted at a single institution in Japan. The target subjects were patients with osteoporosis who started W-TPTD treatment. The subjects who received W-TPTD for 6 months or more were divided into 3 groups: TTT (W-TPTD for 18 months); TBT (sequential treatment of W-TPTD/bisphosphonates/W-TPTD; each for 6 months); and TET (sequential treatment of W-TPTD/elcatonin/W-TPTD, each for 6 months) groups. The efficacy endpoints were bone mineral densities (BMD) in the lumbar spine and femur. RESULTS: Lumbar spine BMD in group TBT increased significantly by 1.6% (P = 0.023), 2.9% (P = 0.001), and 4.4% (P < 0.001) after 6, 12, and 18 months, respectively, compared with baseline values. In group TET, it increased by 2.1%, (P = 0.001), 1.3% (P = 0.066), and 3.0% (P = 0.015) after 6, 12, and 18 months, respectively. A significant increase was observed only after 6 and 18 months. In group TTT, it increased significantly by 3.3% (P = 0.023), 5.1% (P = 0.019), and 7.1% (P = 0.010) after 6, 12, and 18 months, respectively. However, no significant difference in total hip BMD was observed among all three groups. No serious ADRs were reported. CONCLUSION: In patients who discontinue treatment with W-TPTD due to ADRs, sequential treatment with W-TPTD and antiresorptive therapy would be beneficial.
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spelling pubmed-70936832020-03-27 Effects of treatment interruption due to patient convenience on treatment of once a week teriparatide Katahira, Genichiro Akiba, Kotaro Takada, Junichi Iba, Kousuke Yamashita, Toshihiko Osteoporos Sarcopenia Original Article OBJECTIVES: Once-weekly teriparatide (W-TPTD) is an effective drug for patients with osteoporosis; however, some patients discontinue W-TPTD owing to its adverse drug reactions (ADRs). Sequential treatment with W-TPTD and antiresorptive therapy may be effective in treating such patients. In this study, we evaluate the efficacy of this sequential treatment regimen. METHODS: This retrospective study was conducted at a single institution in Japan. The target subjects were patients with osteoporosis who started W-TPTD treatment. The subjects who received W-TPTD for 6 months or more were divided into 3 groups: TTT (W-TPTD for 18 months); TBT (sequential treatment of W-TPTD/bisphosphonates/W-TPTD; each for 6 months); and TET (sequential treatment of W-TPTD/elcatonin/W-TPTD, each for 6 months) groups. The efficacy endpoints were bone mineral densities (BMD) in the lumbar spine and femur. RESULTS: Lumbar spine BMD in group TBT increased significantly by 1.6% (P = 0.023), 2.9% (P = 0.001), and 4.4% (P < 0.001) after 6, 12, and 18 months, respectively, compared with baseline values. In group TET, it increased by 2.1%, (P = 0.001), 1.3% (P = 0.066), and 3.0% (P = 0.015) after 6, 12, and 18 months, respectively. A significant increase was observed only after 6 and 18 months. In group TTT, it increased significantly by 3.3% (P = 0.023), 5.1% (P = 0.019), and 7.1% (P = 0.010) after 6, 12, and 18 months, respectively. However, no significant difference in total hip BMD was observed among all three groups. No serious ADRs were reported. CONCLUSION: In patients who discontinue treatment with W-TPTD due to ADRs, sequential treatment with W-TPTD and antiresorptive therapy would be beneficial. Korean Society of Osteoporosis 2020-03 2020-02-14 /pmc/articles/PMC7093683/ /pubmed/32226827 http://dx.doi.org/10.1016/j.afos.2020.01.001 Text en © 2020 The Korean Society of Osteoporosis. Publishing services by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Katahira, Genichiro
Akiba, Kotaro
Takada, Junichi
Iba, Kousuke
Yamashita, Toshihiko
Effects of treatment interruption due to patient convenience on treatment of once a week teriparatide
title Effects of treatment interruption due to patient convenience on treatment of once a week teriparatide
title_full Effects of treatment interruption due to patient convenience on treatment of once a week teriparatide
title_fullStr Effects of treatment interruption due to patient convenience on treatment of once a week teriparatide
title_full_unstemmed Effects of treatment interruption due to patient convenience on treatment of once a week teriparatide
title_short Effects of treatment interruption due to patient convenience on treatment of once a week teriparatide
title_sort effects of treatment interruption due to patient convenience on treatment of once a week teriparatide
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093683/
https://www.ncbi.nlm.nih.gov/pubmed/32226827
http://dx.doi.org/10.1016/j.afos.2020.01.001
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