Evidence map›Paper›PMID 32935170›Full record

Trial reportOsteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA2021

Forearm bone mineral density and fracture incidence in postmenopausal women with osteoporosis: results from the ACTIVExtend phase 3 trial.

N B Watts, R K Dore, S Baim, B Mitlak, G Hattersley, Y Wang, T D Rozental, M S LeBoff

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase III
In one paragraph

Trial report in Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01657162 (An Extension Study to Evaluate 24 Months of Standard-of-Care Osteoporosis Management Following Completion of 18 Months of BA058 or Placebo Treatment in Protocol BA058-05-003), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01657162 phase3completednot on this map

An Extension Study to Evaluate 24 Months of Standard-of-Care Osteoporosis Management Following Completion of 18 Months of BA058 or Placebo Treatment in Protocol BA058-05-003

TypeinterventionalSponsorRadius Health, Inc.Ran2012 to 2016Enrolled1,139ConditionsPostmenopausal OsteoporosisArmsAlendronate
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. New Challenges: Use and Interpretation of Radius Bone Mineral Density.The Journal of clinical endocrinology and metabolism · 2024
    Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 6 institutions in 1 country.

N B WattsMercy Health Osteoporosis and Bone Health Services, Cincinnati, OH, USA.ORCID https://orcid.org/0000-0003-0719-9801
R K DoreRobin K. Dore, MD, Inc., Tustin, CA, USA.ORCID https://orcid.org/0000-0003-4890-4423
S BaimRush University Medical Center, Chicago, IL, USA.ORCID https://orcid.org/0000-0002-6721-1318
B MitlakRadius Health, Inc., 950 Winter Street, Waltham, MA, 02451, USA. bmitlak@radiuspharm.com.ORCID https://orcid.org/0000-0001-7050-0703
G HattersleyRadius Health, Inc., 950 Winter Street, Waltham, MA, 02451, USA.ORCID https://orcid.org/0000-0001-5487-7703
Y WangRadius Health, Inc., 950 Winter Street, Waltham, MA, 02451, USA.ORCID https://orcid.org/0000-0002-5741-9836
T D RozentalBeth Israel Deaconess Medical Center, Boston, MA, USA.ORCID https://orcid.org/0000-0002-5003-0924
M S LeBoffBrigham and Women's Hospital, Boston, MA, USA.ORCID https://orcid.org/0000-0001-5797-4947
Radius Health (United States) · USBeth Israel Deaconess Medical Center · USBrigham and Women's Hospital · USMercy Health · USRobin Medical (United States) · USRush University Medical Center · US

Funding

Radius Health Inc NCT01657162
6 · The paper itself

Abstract

Abaloparatide increased ultradistal radius bone mineral density (BMD) in the Abaloparatide Comparator Trial in Vertebral Endpoints (ACTIVE) trial. Over the subsequent 24 months in ACTIVExtend, ultradistal radius BMD gains were maintained with alendronate. Conversely, 1/3 radius BMD remained stable during ALN treatment in ACTIVExtend after decreasing during ACTIVE.

introductionAbaloparatide (ABL) increased femoral neck, total hip, and lumbar spine bone mineral density (BMD) in postmenopausal women with osteoporosis and decreased the risk of vertebral and nonvertebral fractures in ACTIVE. Effects on fracture risk and BMD were maintained subsequently with alendronate (ALN) in ACTIVExtend. In a prespecified subanalysis of ACTIVE, ABL also increased BMD at the ultradistal radius. Our objective was to determine the efficacy of ABL followed by ALN vs placebo (PBO) followed by ALN on forearm BMD and fracture risk over 43 months in ACTIVExtend.

methodsUltradistal and 1/3 radius BMD (ACTIVE baseline to month 43) were measured (ABL/ALN, n = 213; PBO/ALN, n = 233). Wrist fracture rates were estimated for the ACTIVExtend intent-to-treat population (ABL/ALN, n = 558; PBO/ALN, n = 581) by Kaplan-Meier (KM) method.

resultsAt cumulative month 25, mean increase from ACTIVE baseline in ultradistal radius BMD was 1.1% (standard error, 0.49%) with ABL/ALN vs - 0.8% (0.43%) with PBO/ALN (P < 0.01). BMD increases with ABL were maintained with ALN through month 43 in ACTIVExtend. BMD decreases at the 1/3 radius in ACTIVE (similar with ABL and PBO) were maintained through 24 months of ALN treatment in ACTIVExtend. Wrist fractures over 43 months occurred in 15 women with ABL/ALN (KM estimate, 2.8%) and 20 with PBO/ALN (KM estimate, 3.6%) (HR = 0.77, 95% CI 0.39, 1.50; P = not significant).

conclusionUltradistal radius BMD gains following treatment with ABL in ACTIVE were maintained over 24 months of ALN treatment in ACTIVExtend. Conversely, 1/3 radius BMD remained stable during ALN treatment in ACTIVExtend after decreasing during ACTIVE.

trial registrationClinicalTrials.gov : NCT01657162 submitted July 31, 2012.

Indexed as

AlendronateBone Density Conservation AgentsOsteoporosis, PostmenopausalOsteoporotic FracturesAgedBone DensityDouble-Blind MethodFemaleForearmHumansIncidenceMiddle AgedPostmenopauseAlendronateBone Density Conservation AgentsAbaloparatideAlendronateBone mineral densityOsteoporosisWrist fracture

Identifiers

PMID32935170
PMCPMC7755646
OpenAlexW3085442632

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.