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Changes in Knee Articular Cartilage Volume in Women on Aromatase Inhibitors

Assessment of Knee Joint Articular Cartilage Volume Change, Bone Loss and Change in Body Composition in Women Treated With Anastrozole or Letrozole and Comparison With Untreated Controls

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00111241
Enrollment
115
Registered
2005-05-19
Start date
2005-05-31
Completion date
2011-12-31
Last updated
2018-12-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthralgia

Keywords

bone fracture, cartilage, osteoporosis, breast cancer, aromatase inhibitors, knee articular cartilage volume

Brief summary

Many women with breast cancer are treated with a class of drugs called aromatase inhibitors (mainly letrozole or anastrozole), which lowers the amount of estrogen being produced in the body. Women on aromatase inhibitors appear to experience joint pains and arthralgia. The aim of this study is to determine whether the joint pains experienced by some women on aromatase inhibitors is associated with more defects in their cartilage, compared to women not receiving this therapy. Using the magnetic resonance imaging (MRI) technique, the knee joint will be examined to assess changes in cartilage volume over time.

Detailed description

The mechanism of increased bone loss and fracture risk is clearly related to the depletion of estrogen production in the bone. But why there is a higher rate of reporting arthralgia, fracture and joint pain amongst women on aromatase inhibitors is not understood. Using magnetic resonance imaging (MRI) to measure knee articular cartilage volume, we have demonstrated that post menopausal hormone therapy used for at least five years is associated with retention of articular cartilage in the knee, indicating that oestrogen may protect against the development of osteoarthritis in post menopausal women. Furthermore, we have recently observed that free testosterone is associated with loss of tibial cartilage, after taking into account age, body mass index, baseline tibial cartilage volume, tibial plateau area and total bone mineral content in healthy men. Whether an excess of testosterone to oestrogen as a consequence of aromatase inhibition has an adverse effect on articular cartilage volume warrants further investigation. This study will include non-hysterectomised women aged 40 to 65 years who have undergone breast surgery and then commenced on aromatase inhibitors within the preceding 12 weeks. The control group (which has been fully recruited) included non-hysterectomised, healthy women aged 40 to 65 years. A MRI of the dominant knee will be used to compare changes in knee articular volume over time. A MRI will be done at baseline and again at 2 years. Changes in knee articular volume is the primary outcome. We will also use this opportunity to compare menopausal symptoms (assessed using the Menopause Quality of Life (MENQOL)questionnaire) between women treated with aromatase inhibitors and those who are not. Well-being will also be assessed using the Psychological General Well-Being index.

Interventions

DRUGaromatase inhibitors (letrozole, anastrozole)

Women prescribed an aromatase inhibitor by their clinician were compared with healthy controls in the community who had been recruited to a prior study

Sponsors

Monash University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
40 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Group 1 : * Aged 40 - 65 * Non-hysterectomised women who have undergone breast surgery * Women on aromatase inhibitors within preceding 12 weeks Group 2 : control group * Healthy, non-hysterectomised women aged 40-65 .

Exclusion criteria

* Previous knee injury requiring non-weight bearing treatment for \> 24 hrs or surgery (including arthroscopy) * Inability to complete the study (eg proposed relocation) * Contraindication to undergoing an MRI including pacemaker, metal sutures, presence of shrapnel, iron filings in eye * Claustrophobia Additional Exclusions for Group 1 * Treatment with tamoxifen for \> 8 weeks prior to commencement * Knee pain lasting for \>24 hours in the last 5 years (prior to commencement on anastrozole or letrozole) * Anastrazole or Letrozole therapy for \> 12 weeks

Design outcomes

Primary

MeasureTime frameDescription
Knee Cartilage VolumeBaseline, two yearschange in medial and lateral articular tibial cartilage volume over two years

Secondary

MeasureTime frameDescription
Knee Subchondral Bone ExpansionBaseline, Two yearschange in subchondral bone expansion area over two years

Countries

Australia

Participant flow

Participants by arm

ArmCount
Women With Breast Cancer on Aromatase Inhibitor Therapy
women with hormone receptor positive breast cancer prescribed an aromatase inhibitor
45
Control
healthy postmenopausal aged-matched controls from prior data base
70
Total115

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyAdverse Event10
Overall StudyLost to Follow-up10
Overall StudyProtocol Violation98
Overall StudyWithdrawal by Subject40

Baseline characteristics

CharacteristicWomen With Breast Cancer on Aromatase Inhibitor TherapyControlTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
45 Participants70 Participants115 Participants
Region of Enrollment
Australia
45 participants70 participants115 participants
Sex: Female, Male
Female
45 Participants70 Participants115 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 450 / 70
serious
Total, serious adverse events
0 / 450 / 70

Outcome results

Primary

Knee Cartilage Volume

change in medial and lateral articular tibial cartilage volume over two years

Time frame: Baseline, two years

ArmMeasureValue (MEAN)Dispersion
Women With Breast CancerKnee Cartilage Volume2042 mm³Standard Deviation 151
ControlKnee Cartilage Volume1971 mm³Standard Deviation 207
Secondary

Knee Subchondral Bone Expansion

change in subchondral bone expansion area over two years

Time frame: Baseline, Two years

ArmMeasureValue (MEAN)Dispersion
Women With Breast CancerKnee Subchondral Bone Expansion2020 mm²Standard Deviation 180
ControlKnee Subchondral Bone Expansion1992 mm²Standard Deviation 204

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026