Sequencing Of Endocrine Therapy In Post-Menopausal Women With Early Breast Cancer (FAST)

This study has been completed.

Sponsor:

Information provided by:

Pfizer

ClinicalTrials.gov Identifier:

NCT01050634

First received: January 13, 2010

Last updated: June 23, 2010

Last verified: June 2010

History of Changes

Results First Received: April 26, 2010

Study Type:	Observational
Study Design:	Observational Model: Case-Only; Time Perspective: Prospective
Condition:	Post Menopausal Women With Early Breast Cancer
Intervention:	Drug: Aromasin (exemestane)

Participant Flow

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Recruitment Details

Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
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Pre-Assignment Details

Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
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Reporting Groups

	Description
Aromasin (Exemestane)	The recommended dosage of exemestane was 25mg once a day.

Participant Flow: Overall Study

	Aromasin (Exemestane)
STARTED	980
Received Treatment	924
COMPLETED	852
NOT COMPLETED	128
Enrolled, but Not Treated	56
Death	2
Adverse Event	42
Lost to Follow-up	2
Unknown	21
Ongoing at Date of Cut-Off	5

Baseline Characteristics

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Reporting Groups

	Description
Aromasin (Exemestane)	The recommended dosage of exemestane was 25 mg once a day.

Baseline Measures

	Aromasin (Exemestane)
Number of Participants [units: participants]	924
Age, Customized [units: Participants]
18-44 years	24
45-64 years	450
>= 65 years	417
Unspecified	33
Gender [units: Participants]
Female	924
Male	0

Outcome Measures

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1. Primary:

Change From Baseline in International Breast Cancer Study Group (IBCSG) Linear Analogues Self-Assessment (LASA) Quality of Life (QoL) Core Questionnaire Scores [ Time Frame: Baseline, Month 12 ]

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2. Primary:

Change From Baseline in Thickness of Endometrium [ Time Frame: Baseline, Month 12 ]

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Measure Type	Primary
Measure Title	Change From Baseline in Thickness of Endometrium
Measure Description	Ultrasound measurement. New derived variable for normalization of endometrium thickness: 1 = Endometrium thickness <=5mm 0 = Endometrium thickness >5mm
Time Frame	Baseline, Month 12
Safety Issue	No

Population Description

Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
FAS. Missing values were imputed by LOCF. Number of participants analyzed=Number of subjects with Baseline and Final Visit (LOCF) values.

Reporting Groups

	Description
Aromasin (Exemestane)	The recommended dosage of exemestane was 25 mg once a day.

Measured Values

	Aromasin (Exemestane)
Number of Participants Analyzed [units: participants]	437
Change From Baseline in Thickness of Endometrium [units: mm] Mean ± Standard Deviation	-1.1 ± 6.1

No statistical analysis provided for Change From Baseline in Thickness of Endometrium

3. Primary:

Change From Baseline in IBCSG LASA Items Scores - QoL Module 24-26 [ Time Frame: Baseline, Month 12 ]

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4. Primary:

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 [ Time Frame: Baseline, Month 12 ]

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5. Primary:

Change From Baseline in IBCSG Vaginal Symptoms - QoL Module 24-26 [ Time Frame: Baseline, Month 12 ]

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Serious Adverse Events

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Other Adverse Events

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More Information

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Certain Agreements:

Principal Investigators are NOT employed by the organization sponsoring the study.

There IS an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

The agreement is:

	The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is less than or equal to 60 days. The sponsor cannot require changes to the communication and cannot extend the embargo.
	The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is more than 60 days but less than or equal to 180 days. The sponsor cannot require changes to the communication and cannot extend the embargo.
	Other disclosure agreement that restricts the right of the PI to discuss or publish trial results after the trial is completed. Restriction Description: Pfizer has the right to review disclosures, requesting a delay of less than 60 days. Investigator will postpone single center publications until after disclosure of pooled data (all sites), less than 12 months from study completion/termination at all participating sites. Investigator may not disclose previously undisclosed confidential information other than study results.

Limitations and Caveats

Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
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Results Point of Contact:

Name/Title: Pfizer ClinicalTrials.gov Call Center
Organization: Pfizer, Inc.
phone: 1-800-718-1021
e-mail: ClinicalTrials.gov_Inquiries@pfizer.com

No publications provided

Responsible Party:	Director, Clinical Trial Disclosure Group, Pfizer, Inc.
ClinicalTrials.gov Identifier:	NCT01050634 History of Changes
Other Study ID Numbers:	A5991079
Study First Received:	January 13, 2010
Results First Received:	April 26, 2010
Last Updated:	June 23, 2010
Health Authority:	United States: Institutional Review Board

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