Literature DB >> 28176386

Long-Term Randomized Trial of Intensive Versus Symptomatic Management in Paget's Disease of Bone: The PRISM-EZ Study.

Adrian Tan1, Kirsteen Goodman2, Allan Walker2, Jemma Hudson3, Graeme S MacLennan3, Peter L Selby4,5, William D Fraser6, Stuart H Ralston1,2.   

Abstract

It has been suggested that normalization of bone turnover may improve clinical outcome in Paget's disease of bone (PDB) by preventing complications such as fractures and the development of osteoarthritis. Here we investigated the long-term effects of a treatment strategy that aimed to normalize bone turnover in PDB with that of symptomatic treatment. The study group comprised 502 subjects who were enrolled into a 3-year extension of the Paget's Disease: Randomized Trial of Intensive versus Symptomatic Management (PRISM) study. Intensive bisphosphonate therapy was continued in 270 of these subjects with the aim of normalizing bone turnover using zoledronic acid as the treatment of first choice. Symptomatic treatment continued in 232 subjects in whom bisphosphonates were only given for the treatment of bone pain. The primary outcome was fracture and secondary outcomes were orthopedic procedures, quality of life, and bone pain, adjusted for baseline characteristics. Serum total alkaline phosphatase (ALP) concentrations were significantly lower in the intensive group on entry to the study and the differences between groups increased as the study progressed. There were no clinically important differences in quality of life measures or bone pain between the treatment groups. Intensive treatment was associated with a nonsignificant increase in fracture risk (hazard ratio = 1.90; 95% CI, 0.91 to 3.98; p = 0.087), orthopedic procedures (1.81; 95% CI, 0.71 to 4.61; p = 0.214), and serious adverse events (relative risk 1.28; 95% CI, 0.96 to 1.42). We conclude that long-term intensive bisphosphonate therapy confers no clinical benefit over symptomatic therapy and is associated with a nonsignificant increase in the risk of fractures, orthopedic events, and serious adverse events. The results of this study suggest that in patients with established PDB, bisphosphonate therapy should focus on control of symptoms rather than suppression of bone turnover.
© 2016 American Society for Bone and Mineral Research. © 2016 American Society for Bone and Mineral Research.

Entities:  

Keywords:  BISPHOSPHONATES; CLINICAL TRIAL; PAGET'S DISEASE OF BONE; QUALITY OF LIFE; TREATMENT

Mesh:

Substances:

Year:  2017        PMID: 28176386     DOI: 10.1002/jbmr.3066

Source DB:  PubMed          Journal:  J Bone Miner Res        ISSN: 0884-0431            Impact factor:   6.741


  14 in total

1.  Long-term control of Paget's disease of bone with low-dose, once-weekly, oral bisphosphonate preparations, in a "real world" setting.

Authors:  Yair Liel; Muhammad Abu Tailakh
Journal:  Endocrine       Date:  2018-11-08       Impact factor: 3.633

Review 2.  Paget's Disease of Bone.

Authors:  Luigi Gennari; Domenico Rendina; Alberto Falchetti; Daniela Merlotti
Journal:  Calcif Tissue Int       Date:  2019-01-23       Impact factor: 4.333

Review 3.  [Paget's disease of bone-a current review of clinical aspects, diagnostics and treatment].

Authors:  P Klemm; G Dischereit; S von Gerlach; U Lange
Journal:  Z Rheumatol       Date:  2020-10-01       Impact factor: 1.372

4.  Epigenetic DNA Methylation Signatures Associated With the Severity of Paget's Disease of Bone.

Authors:  Ilhame Diboun; Sachin Wani; Stuart H Ralston; Omar M E Albagha
Journal:  Front Cell Dev Biol       Date:  2022-06-13

Review 5.  Bisphosphonates for Paget's disease of bone in adults.

Authors:  Luis Corral-Gudino; Adrian Jh Tan; Javier Del Pino-Montes; Stuart H Ralston
Journal:  Cochrane Database Syst Rev       Date:  2017-12-01

6.  Antibody Response to Paramyxoviruses in Paget's Disease of Bone.

Authors:  Micaela Rios Visconti; Ricardo Usategui-Martín; Stuart H Ralston
Journal:  Calcif Tissue Int       Date:  2017-03-31       Impact factor: 4.333

7.  Paget's Disease: Skeletal Manifestations and Effect of Bisphosphonates.

Authors:  Ho Kang; Young-Chang Park; Kyu Hyun Yang
Journal:  J Bone Metab       Date:  2017-05-31

8.  Zoledronic acid prevents pagetic-like lesions and accelerated bone loss in the p62P394L mouse model of Paget's disease.

Authors:  Anna Daroszewska; Lorraine Rose; Nadine Sarsam; Gemma Charlesworth; Amanda Prior; Kenneth Rose; Stuart H Ralston; Robert J van 't Hof
Journal:  Dis Model Mech       Date:  2018-08-23       Impact factor: 5.758

Review 9.  Diagnosis and Management of Paget's Disease of Bone in Adults: A Clinical Guideline.

Authors:  Stuart H Ralston; Luis Corral-Gudino; Cyrus Cooper; Roger M Francis; William D Fraser; Luigi Gennari; Núria Guañabens; M Kassim Javaid; Robert Layfield; Terence W O'Neill; R Graham G Russell; Michael D Stone; Keith Simpson; Diana Wilkinson; Ruth Wills; M Carola Zillikens; Stephen P Tuck
Journal:  J Bone Miner Res       Date:  2019-02-25       Impact factor: 6.741

10.  Zoledronate in the prevention of Paget's (ZiPP): protocol for a randomised trial of genetic testing and targeted zoledronic acid therapy to prevent SQSTM1-mediated Paget's disease of bone.

Authors:  Owen Cronin; Laura Forsyth; Kirsteen Goodman; Steff C Lewis; Catriona Keerie; Allan Walker; Mary Porteous; Roseanne Cetnarskyj; Lakshminarayan R Ranganath; Peter L Selby; Geeta Hampson; Rama Chandra; Shu Ho; Jon H Tobias; Steven Young-Min; Malachi J McKenna; Rachel K Crowley; William D Fraser; Luigi Gennari; Ranuccio Nuti; Maria Luisa Brandi; Javier Del Pino-Montes; Jean-Pierre Devogelaer; Anne Durnez; Giancarlo Isaia; Marco Di Stefano; Núria Guañabens; Josep Blanch; Markus J Seibel; John P Walsh; Mark A Kotowicz; Geoffrey C Nicholson; Emma L Duncan; Gabor Major; Anne Horne; Nigel L Gilchrist; Maarten Boers; Gordon D Murray; Keith Charnock; Diana Wilkinson; R Graham G Russell; Stuart H Ralston
Journal:  BMJ Open       Date:  2019-09-04       Impact factor: 2.692

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