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Bone Loss after Allogeneic Haematopoietic Stem Cell Transplantation: A Pilot Study on the Use of Zoledronic Acid

Purpose. Bone loss is a common phenomenon following allogeneic haematopoietic stem cell transplantation (allo-HSCT). The study aimed on tolerance and efficacy of zoledronic acid (ZA) in patients after allo-HSCT. Methods. 40 patients' with osteoporosis or osteopenia were recruited on this phase...

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Autores principales: Hausmann, Andreas, Hill, Wolfgang, Stemmler, Hans Joachim, Ledderose, Georg, Baur-Melnyk, Andrea, Fritsch, Susanne, Ullmann, Johanna, Kolb, Hans-Jochem, Geiger, Sandra, Tischer, Johanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3328888/
https://www.ncbi.nlm.nih.gov/pubmed/22550587
http://dx.doi.org/10.1155/2012/858590
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author Hausmann, Andreas
Hill, Wolfgang
Stemmler, Hans Joachim
Ledderose, Georg
Baur-Melnyk, Andrea
Fritsch, Susanne
Ullmann, Johanna
Kolb, Hans-Jochem
Geiger, Sandra
Tischer, Johanna
author_facet Hausmann, Andreas
Hill, Wolfgang
Stemmler, Hans Joachim
Ledderose, Georg
Baur-Melnyk, Andrea
Fritsch, Susanne
Ullmann, Johanna
Kolb, Hans-Jochem
Geiger, Sandra
Tischer, Johanna
author_sort Hausmann, Andreas
collection PubMed
description Purpose. Bone loss is a common phenomenon following allogeneic haematopoietic stem cell transplantation (allo-HSCT). The study aimed on tolerance and efficacy of zoledronic acid (ZA) in patients after allo-HSCT. Methods. 40 patients' with osteoporosis or osteopenia were recruited on this phase II study. ZA was given at a dose of 4 mg IV every 3 months for 2 years (yrs). BMD was determined by dual-energy X-ray absorptiometry (LS lumbar spine, FH femur hip). Patients were evaluated for deoxypyridinoline (Dpd) and calcium excretion by longitudinal measurements. Results. 36 patients who had received at least 3 doses of ZA were evaluable. 26 patients had at least two BMD measurements since baseline (BMD group). Among these patients, BMD increased from 0.97 ± 0.15 to 1.10 ± 0.18 g/cm² (LS baseline—2 yrs, Δ+11.6 ± 6.0%, P < 0.001) and from 0.82 ± 0.10 to 0.91 ± 0.10 g/cm(²) (FH baseline—2 yrs, Δ+7.5 ± 7.0%, P < 0.001). Factors associated with an increase in BMD were younger age, female donor sex, and immunosuppression with CSA/MTX. Conclusion. ZA was generally well tolerated; it increases BMD and reduces Dpd excretion significantly in patients with bone loss after allo-HSCT.
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spelling pubmed-33288882012-05-01 Bone Loss after Allogeneic Haematopoietic Stem Cell Transplantation: A Pilot Study on the Use of Zoledronic Acid Hausmann, Andreas Hill, Wolfgang Stemmler, Hans Joachim Ledderose, Georg Baur-Melnyk, Andrea Fritsch, Susanne Ullmann, Johanna Kolb, Hans-Jochem Geiger, Sandra Tischer, Johanna Chemother Res Pract Clinical Study Purpose. Bone loss is a common phenomenon following allogeneic haematopoietic stem cell transplantation (allo-HSCT). The study aimed on tolerance and efficacy of zoledronic acid (ZA) in patients after allo-HSCT. Methods. 40 patients' with osteoporosis or osteopenia were recruited on this phase II study. ZA was given at a dose of 4 mg IV every 3 months for 2 years (yrs). BMD was determined by dual-energy X-ray absorptiometry (LS lumbar spine, FH femur hip). Patients were evaluated for deoxypyridinoline (Dpd) and calcium excretion by longitudinal measurements. Results. 36 patients who had received at least 3 doses of ZA were evaluable. 26 patients had at least two BMD measurements since baseline (BMD group). Among these patients, BMD increased from 0.97 ± 0.15 to 1.10 ± 0.18 g/cm² (LS baseline—2 yrs, Δ+11.6 ± 6.0%, P < 0.001) and from 0.82 ± 0.10 to 0.91 ± 0.10 g/cm(²) (FH baseline—2 yrs, Δ+7.5 ± 7.0%, P < 0.001). Factors associated with an increase in BMD were younger age, female donor sex, and immunosuppression with CSA/MTX. Conclusion. ZA was generally well tolerated; it increases BMD and reduces Dpd excretion significantly in patients with bone loss after allo-HSCT. Hindawi Publishing Corporation 2012 2012-04-10 /pmc/articles/PMC3328888/ /pubmed/22550587 http://dx.doi.org/10.1155/2012/858590 Text en Copyright © 2012 Andreas Hausmann et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Hausmann, Andreas
Hill, Wolfgang
Stemmler, Hans Joachim
Ledderose, Georg
Baur-Melnyk, Andrea
Fritsch, Susanne
Ullmann, Johanna
Kolb, Hans-Jochem
Geiger, Sandra
Tischer, Johanna
Bone Loss after Allogeneic Haematopoietic Stem Cell Transplantation: A Pilot Study on the Use of Zoledronic Acid
title Bone Loss after Allogeneic Haematopoietic Stem Cell Transplantation: A Pilot Study on the Use of Zoledronic Acid
title_full Bone Loss after Allogeneic Haematopoietic Stem Cell Transplantation: A Pilot Study on the Use of Zoledronic Acid
title_fullStr Bone Loss after Allogeneic Haematopoietic Stem Cell Transplantation: A Pilot Study on the Use of Zoledronic Acid
title_full_unstemmed Bone Loss after Allogeneic Haematopoietic Stem Cell Transplantation: A Pilot Study on the Use of Zoledronic Acid
title_short Bone Loss after Allogeneic Haematopoietic Stem Cell Transplantation: A Pilot Study on the Use of Zoledronic Acid
title_sort bone loss after allogeneic haematopoietic stem cell transplantation: a pilot study on the use of zoledronic acid
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3328888/
https://www.ncbi.nlm.nih.gov/pubmed/22550587
http://dx.doi.org/10.1155/2012/858590
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