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Reassessment of fracture risk in women after 3 years of treatment with zoledronic acid: when is it reasonable to discontinue treatment?

Identifieur interne : 003510 ( Ncbi/Merge ); précédent : 003509; suivant : 003511

Reassessment of fracture risk in women after 3 years of treatment with zoledronic acid: when is it reasonable to discontinue treatment?

Auteurs : Felicia Cosman ; Jane A. Cauley ; Richard Eastell ; Steven Boonen ; Lisa Palermo ; Ian R. Reid ; Steven R. Cummings ; Dennis M. Black

Source :

RBID : pubmed:25215556

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English descriptors

Abstract

Data are needed to guide therapeutic decisions about stopping bisphosphonates after an initial treatment period.

DOI: 10.1210/jc.2014-1971
PubMed: 25215556

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pubmed:25215556

Le document en format XML

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<term>Bone Density Conservation Agents (therapeutic use)</term>
<term>Diphosphonates (administration & dosage)</term>
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<div type="abstract" xml:lang="en">Data are needed to guide therapeutic decisions about stopping bisphosphonates after an initial treatment period.</div>
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<Month>12</Month>
<Day>06</Day>
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<DateCompleted>
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<Month>10</Month>
<Day>07</Day>
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<Year>2017</Year>
<Month>11</Month>
<Day>06</Day>
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<Title>The Journal of clinical endocrinology and metabolism</Title>
<ISOAbbreviation>J. Clin. Endocrinol. Metab.</ISOAbbreviation>
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<ArticleTitle>Reassessment of fracture risk in women after 3 years of treatment with zoledronic acid: when is it reasonable to discontinue treatment?</ArticleTitle>
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<AbstractText Label="CONTEXT" NlmCategory="BACKGROUND">Data are needed to guide therapeutic decisions about stopping bisphosphonates after an initial treatment period.</AbstractText>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">To define significant predictors of fracture and quantify fracture incidence in risk factor-defined subgroups of women who discontinue zoledronic acid (ZOL) after 3 years of treatment. To determine if continuing ZOL reduces fracture risk in subgroups.</AbstractText>
<AbstractText Label="DESIGN" NlmCategory="METHODS">This study is based on data from the 3 year extension of HORIZON.</AbstractText>
<AbstractText Label="SETTING" NlmCategory="METHODS">Subjects were in the ZOL arm of the Multicenter HORIZON trial.</AbstractText>
<AbstractText Label="PARTICIPANTS" NlmCategory="METHODS">One thousand two hundred thirty three women who previously received 3 ZOL treatments during the Core trial.</AbstractText>
<AbstractText Label="INTERVENTION" NlmCategory="METHODS">Randomization to three additional annual ZOL (Z6, n = 616) or placebo infusions (Z3P3, n = 617).</AbstractText>
<AbstractText Label="MAIN OUTCOMES" NlmCategory="RESULTS">The risk of morphometric vertebral fractures (MorphVertFx) and clinical nonvertebral fractures (NVF).</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The incidence of MorphVertFx in Z3P3 was predicted by femoral neck (FN) t-score ≤-2.5 [OR 3.3 (1.4, 8.0), p = .008], total hip (TH) t-score ≤-2.5 [OR 4.0 (1.8, 9.0), p = .0007], and incident MorphVertFx during Core [OR 4.75 (1.4, 16.8), p < .015]. Incidence of NVF was predicted by TH t-score [for 1 decline, HR 1.7 (1.2, 2.6), p = .008], incident NVF during Core [HR 2.5 (1.2, 5.3), p = .014], and prevalent vertebral fracture [HR 3.0 (1.4, 6.3), p = .005]. For MorphVertFx, there were no significant treatment subgroup interactions; absolute fracture reductions with continued ZOL were greatest in high-risk subgroups. For NVF, there were no significant treatment reductions overall or in subgroups and no significant interactions.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">After 3 years of ZOL, in women who have a TH t-score above -2.5, no recent incident fracture and no more than one risk factor (almost 55% of the population), risk for subsequent fracture (over three additional years) is low if treatment is discontinued (for MorphVertFx, average risk 3.2% and for NVF, average risk 5.8%). In these patients, discontinuation for up to 3 years is reasonable.</AbstractText>
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<RefSource>Ann Clin Biochem. 2015 Jan;52(1):183</RefSource>
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