Title: Steering Committee meeting, 24th September 2005
1Steering Committee meeting, 24th September
2005 University of Oxford Examination Schools
2ATLAS and aTTom
adjuvant Tamoxifen Treatment offer more?
3ATLAS and aTTom study design
- After several years on adjuvant tamoxifen,
- patient and doctor both SUBSTANTIALLY UNCERTAIN
- about whether to stop now or continue
- RANDOMISE
- STOP tamoxifen now CONTINUE for at least
- 5 more years
4Sample size sought
- To confirm, or refute, a 3 difference in
absolute survival (e.g. 75 to 78), 8,000
patients would have to be randomised to have a
90 chance of detecting this difference (at a 5
statistical significance level) between the two
groups. - To detect a 2 difference in absolute survival
(e.g. 75 to 77), 20,000 patients would be
needed.
5Completion of recruitment phase in ATLAS and aTTom
- January 2005 ATLAS Steering Committee (TSC) with
the aTTom TSC decided to close accrual - gt 20,000 women now randomised in studies of 10 vs
5 years of tamoxifen - aTTom and ATLAS closed to recruitment in March
2005.
612898
2354
715 254 women randomised from 30 countries
largest cancer treatment trial so far!
8Cumulative recruitment figures into aTTom by
prior duration of tamoxifen
9Accrual in trials of 10 vs 5 years of tamoxifen
10Baseline data of women randomised in ATLAS
- Identifiers
- Responsible doctor
- Patient name
- Date of birth
- Hospital number
- National identification number
- Address
- Alternative contact details
- Clinical
- Date of diagnosis
- ER status
- Nodal status
- Recurrence (including contralateral breast
cancer) - Other primary cancer
- Menopausal status
- Ovarian ablation
- Dose of tamoxifen (daily) and prior duration
11AGE DISTRIBUTION
STOP CONTINUE
12NODAL STATUS
STOP CONTINUE
13ER status
14Distribution of ER status in ATLAS
- ATLAS
- Older (n2354)
- ER poor 9
- ER unknown 68
- ER positive 23
- Newer (n12898)
- ER poor 10
- ER unknown 37
- ER positive 53
15Survival among women in the older and newer
components of ATLAS
NB Women in STOP and CONTINUE arms combined in
each component ie this is non-randomised
16Survival in ATLAS by nodal status
17Survival in ATLAS by ER status
18ATLAS the next few years
- Compliance with random allocation
- Completeness of follow-up
- At present, women with a prior duration of 4 or
more years of tamoxifen before randomisation have
a median follow-up of 3 years. - An absolute minimum of five more years of
follow-up is needed for a proper assessment of
the benefits and risks of long-term tamoxifen.
19Numbers of women where follow-up should be data
available
Denominators for main breast cancer analyses H
Denominators for main side-effect analyses
20Compliance in older part of ATLAS
21Compliance in newer part of ATLAS
22Completeness of follow-up data
- We must have up to date information on all women
especially with respect to - - Compliance
- - Recurrence
- - Death (and if died, date and cause of death)
- - Other primary cancers
23Quality of follow-up data
- All forms should be completed in full!
- At least 80 of the ATLAS offices time is spent
chasing follow-up queries
24Most common problems with follow-up forms
- Not returned!
- Not completed in full
- Doctors writing Lost to follow-up
- Dates of events missing
- Cause of death not provided
- Hospital admission diagnosis and date missing
25Use the information we have to help ensure
long-term follow-up
- Identifiers
- Responsible doctor
- Patient name
- Date of birth
- Hospital number
- National identification number
- Address
- Alternative contact details
26 SummaryLong-term follow-up and good
compliance are required in ATLASIf we can get
these, we will get a reliable answer on whether
longer versus shorter tamoxifen improves survival
among women with early breast cancer
27(No Transcript)
28- I want to thank everyone personally for all they
have done to make this collaboration work! - Dr Christina Davies, ATLAS Coordinator
- For further information on any of this
presentation, please contact atlas_at_ctsu.ox.ac.uk