ibcsg trial viii · 2019. 11. 15. · ibcsg viii: rationale of the study in the mid-1980ies: •...
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IBCSG Trial VIIIAdjuvant Chemotherapy, Goserelin,
or Their Sequential Combinationfor Pre/Perimenopausal Patients with
Node-negative Breast Cancer
International Breast Cancer Study Group
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IBCSG VIII:Rationale of the Study
In the mid-1980ies:• Some beneficial effect of ovarian ablation,
considered overtreatment for N-• Chemotherapy beneficial especially for
premenopausal women with N+ disease• The majority of patients with N- disease were
offered no adjuvant treatment after surgery• CT-induced amenorrhea associated with
improved DFS (limited duration and permanent)
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IBCSG VIII: Aims
To test the therapeutic role of short duration ovarian function suppression in pre-/perimenopausal patients with N- breast cancer by asking the following questions:
• Could LH-RH analogue (x 24) be as effective as CMF x 6 alone?
• Could the sequence (CMF x 6 → LH-RH analogue x 18) improve results compared with CMF alone?
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IBCSG Trial VIIIPre/perimenopausal, node-negative diseaseAccrual: 1990-1999; Total patients: 1111
StrataRANDOMIZE
No adjuvant therapy (drop 4/92)
Goserelin x 24 mos.
CMFx6
CMFx6 → Goserelin x 18 mos.
Institution
ER status
RT
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IBCSG VIII: Statistical Considerations
• Primary endpoint: DFS• 224 events for 80% power• 202 events in current analysis• Median follow-up: 5.8 years
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IBCSG VIII: Patient CharacteristicsGoserelin
x 24CMF x 6 CMF x 6 →
Goserelin x 18Patients 346 360 357
Age at entry≤ 39 y 20% 19% 21%40 – 49 y 63% 66% 61%≥ 50 y 17% 15% 18%
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IBCSG VIII: Patient Characteristics
Goserelin CMF x 6 CMF x 6x 24 Goserelin x 18
Tumor size≤ 2 cm 61% 60% 63%> 2 cm 38% 39% 36%unknown 1% 1% 1%
Nodes examinedmedian 16 16 16
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IBCSG VIII: Patient Characteristics
Goserelin CMF x6 CMFx6x 24 Goserelin x 18
ER-status
Absent: 0 11% 10% 11%
Low: 1-9 19% 19% 17%
Positive: 10+ 66% 68% 68%
Unknown 4% 3% 3%
ER-absent plus ER-low were stratified as ER-negative
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IBCSG VIII: ComplianceGoserelin
Goserelin x 24 CMF x 6 Goserelin x 18
Total patients 346 357Completed goserelin 281 (82%) 274 (77%)No goserelin 10 (3%) 36 (10%)Incomplete goserelin 55 (15%) 48 (13%)
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IBCSG VIII: ComplianceCMF
CMFx6 CMFx6 Goserelin x 18
Total Patients 360 357Completed CMFx6 327 (90%) 320 (89%)No Chemotherapy 6 (2%) 11 (3%)<6 cycles of CMF 28 (8%) 27 (8%)
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IBCSG VIII: Cessation of Menses Age ≥ 40
No Rx Gos CMFx6 CMF-Gos
0
10
20
30
40
50
60
70
80
90
100
1 4 7 10 13 16 19 22 25 28 31 34
Month from Randomization
Perc
ent w
ithou
t Men
ses
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IBCSG VIII: Cessation of MensesAge ≤ 39
0
10
20
30
40
50
60
70
80
90
100
1 4 7 10 13 16 19 22 25 28 31 34
Month from Randomization
Perc
ent w
ithou
t Men
ses
No Rx Gos CMFx6 CMF-Gos
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IBCSG VIII: DFS and OS
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IBCSG VIII: DFS by ER
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IBCSG VIII: DFS for ER+ by Age
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IBCSG VIII: STEPP for ER+ CMF vs. Goserelin
Median Age of Subpopulations
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IBCSG VIII: STEPP for ER+ CMF→ Goserelin vs. CMF
Median Age of Subpopulations
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IBCSG VIII: STEPP for ER+ CMF→ Goserelin vs. Goserelin
Median Age of Subpopulations
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IBCSG VIII Conclusions (1)
• IBCSG VIII: patient selection by risk (N-) rather than endocrine responsiveness
• Treatment effects appear to differ according to ER-status and age.
• As expected now, goserelin alone is less effective than CMF containing regimens for the ER– cohort.
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IBCSG VIII Conclusions (2)
For ER+ cohort (conclusions less certain):
• No tamoxifen was given and goserelinwas only administered for up to 2 years.
• Results for goserelin and CMF are similar.
• The sequence of CMF → goserelin may reduce the risk of an event compared with either modality alone, especially for younger patients.
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Tailored Treatment InvestigationsPremenopausal patients with endocrine-responsive disease
(ER > 10% and/or PgR > 10%)
SOFT: Suppression of Ovarian Function Trial (BIG 2-02)tamoxifen vs OFS + tamoxifen vs OFS + exemestane
TEXT: Tamoxifen and Exemestane Trial (BIG 3-02)OFS + tamoxifen vs OFS + exemestane
PERCHE: Premenopausal Endocrine-Responsive Chemotherapy Trial (BIG 4–02)
CT + OFS + tam/exe vs OFS + tam/exe
SOFT and TEXT include North American Intergroup participationCoordinating Group: International Breast Cancer Study Group (IBCSG)Pharmaceutical Partner: Pharmacia
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Thanks to patients, physicians, nurses, and data managers of the IBCSG
• Australia New Zealand (ANZ 5 centers)• Swiss Group (SAKK 8 centers)• Ljubljana (Slovenia)• Aviano (Italy)• Madrid (Spain)• Cape Town (R. of S. Africa)• Göteborg (Sweden)• Milan (Italy)• Brescia (Italy)• Vicenza (Italy)• …and many other members of the IBCSG