Sequencing Of Endocrine Therapy In Post-Menopausal Women With Early Breast Cancer (FAST)
- Conditions
- Post Menopausal Women With Early Breast Cancer
- Interventions
- Registration Number
- NCT01050634
- Lead Sponsor
- Pfizer
- Brief Summary
Quality of life under therapy with Aromasin® (exemestane) according to IBCSG (International Breast Cancer Study Group) questionnaire.
Change of the endometrium after switching from tamoxifen to Aromasin® (exemestane).
Deeper knowledge of Adverse Events during routine administration.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 980
- Early Breast Cancer, post-menopausal, 2-3 yrs adjuvant tamoxifen therapy.
- Not applicable.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Observational Aromasin (exemestane) -
- Primary Outcome Measures
Name Time Method Change From Baseline in International Breast Cancer Study Group (IBCSG) Linear Analogues Self-Assessment (LASA) Quality of Life (QoL) Core Questionnaire Scores Baseline, Month 12 10 single-item in LASA format(100mm scale): Physical wellbeing (good to lousy); Mood (happy to miserable); Tiredness, Hot flushes, Feeling sick, Use of arm restricted - all none to a lot; Appetite (good to none); Effort to cope with illness (no effort to great deal of effort); Supported by people (much to not at all); Rating life in current condition (perfect to worst health). Individual items scored by measuring distance in mm between left scale anchor and patient's mark, where best QoL=0mm, worst QoL =100mm, and negative changes from baseline=improvement in QoL.Score range=0-100
Change From Baseline in Thickness of Endometrium Baseline, Month 12 Ultrasound measurement. New derived variable for normalization of endometrium thickness:
1 = Endometrium thickness \<=5mm 0 = Endometrium thickness \>5mmChange From Baseline in IBCSG LASA Items Scores - QoL Module 24-26 Baseline, Month 12 Assessment of severity of 13 items (Being irritable, Sweats, Vaginal discharge, dryness, and itching/irritation, Sleep disturbance, Feeling dizzy, Headaches, Bone or joint pain, Troubled by weight gain, Loss of sexual interest, Difficulties in becoming aroused - all from none to severe, and Bothered by treatment related difficulties (not at all to severely). Individual items scored by measuring distance in mm between left scale anchor and patient's mark, where no severity=0mm, maximum severity=100mm and negative changes from baseline=lessening of severity.Score range=0-100
Change From Baseline in 12-Item Short Form Health Survey (SF-12) Summary Subscales (Physical Summary Scale Derived From Items 1-5, 8 and Mental Summary Scale Derived From Items 6, 7, 9-11) Scores Baseline, Month 12 Items: 1.General health 1=poor to 5=excellent 2.Limited moderate activities \& 3.Climbing of stairs 1=lot to 3=not at all 4.Accomplished less \& 5.Limited in kind of work due to physical health, 6.Accomplished less \& 7.Work done less carefully due to emotional problems 1=yes, 2=no 8.Pain interfered with work 1=extremely to 5=not at all 9.Felt calm \& 10.Had lot of energy 1=none to 6=all time 11.Felt downhearted \& 12.Physical health/emotional problems interfered with social activities 1=all time to 6=none of the time. Higher scores=better QoL, positive changes from baseline=improvement in QoL.
Change From Baseline in IBCSG Vaginal Symptoms - QoL Module 24-26 Baseline, Month 12 The 3 LASA items concerning vaginal symptoms (discharge, dryness, itching/irritation) were combined as the sum of these 3 items. Lower scores corresponded to better QoL, with negative changes from baseline corresponding to improvements in vaginal symptoms. Total overall score range=0-300, Best score=0, Worst score=300
- Secondary Outcome Measures
Name Time Method