Basic Trial Information
Trial Description
     Summary
     Further Trial Information
     Eligibility Criteria
Trial Contact Information

Basic Trial Information

Phase Type Status Age Sponsor Protocol IDs Phase IV Diagnostic, Supportive care, Treatment Active 40 to 65 Other 2004/949 NCT00111241

Trial Description

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.

Further Study Information

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.

Eligibility Criteria

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

Trial Contact Information

Trial Lead Organizations/Sponsors

Monash Medical Center - Clayton Campus

Susan Davis, MBBS FRACP PhD

Principal Investigator

Australia
Victoria
	Melbourne
	Monash Medical Center - Clayton Campus
		Susan Davis, Professor	Ph: +61 3 9903 0827
			Email: susan.davis@med.monash.edu.au
		Rebecca Ades, MPH	Ph: +61 3 9903 0827
			Email: Rebecca.ades@med.monash.edu.au
		Robin Bell, MBBS PhD MPH FAFPHM	Sub-Investigator
		Susan Davis, MBBS FRACP PhD	Principal Investigator

Link to the current ClinicalTrials.gov record.
NLM Identifer NCT00111241
Information obtained from ClinicalTrials.gov on May 27, 2008