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Clinical Trial
. 2019 Jul 1;145(1):274-283.
doi: 10.1002/ijc.32093. Epub 2019 Jan 16.

Efficacy of anastrozole after tamoxifen in early breast cancer patients with chemotherapy-induced ovarian function failure

Affiliations
Clinical Trial

Efficacy of anastrozole after tamoxifen in early breast cancer patients with chemotherapy-induced ovarian function failure

Irene E G van Hellemond et al. Int J Cancer. .

Abstract

The DATA study (NCT00301457) compared 6 and 3 years of anastrozole in postmenopausal women with hormone receptor-positive early breast cancer after 2-3 years of tamoxifen. Patients with chemotherapy-induced ovarian function failure (CIOFF) were also eligible, but could be at risk of ovarian function recovery (OFR). The current analysis compared the survival of women with CIOFF with definitely postmenopausal women and examined the influence of OFR on survival. Therefore, we selected patients from the DATA study aged 45-57 years at randomization who had received (neo)adjuvant chemotherapy. They were classified by reversibility of postmenopausal status: possibly reversible in case of CIOFF (n = 395) versus definitely postmenopausal (n = 261). The former were monitored by E2 measurements for OFR. The occurrence of OFR was incorporated as a time-dependent covariate in a Cox-regression model for calculating the hazard ratio (HR). We used the landmark method to calculate residual 5-year survival rates. When comparing CIOFF women with definitely postmenopausal women, the survival was not different. Among CIOFF women with available E2 follow-up values (n = 329), experiencing OFR (n = 39) had an unfavorable impact on distant recurrence-free survival (HR 2.27 [95% confidence interval [CI] 0.98-5.25; p = 0.05] and overall survival (HR 2.61 [95% CI 1.11-6.13; p = 0.03]). After adjusting for tumor features, the HRs became 2.11 (95% CI 0.89-5.02; p = 0.09) and 2.24 (95% CI 0.92-5.45; p = 0.07), respectively. The residual 5-year rate for distant recurrence-free survival was 76.9% for women with OFR and 92.1% for women without OFR, and for 5-year overall survival 80.8% and 94.4%, respectively. Women with CIOFF receiving anastrozole may be at increased risk of disease recurrence if experiencing OFR.

Keywords: aromatase inhibitor; breast cancer; chemotherapy-induced amenorrhea; chemotherapy-induced ovarian function failure (CIOFF); ovarian function recovery (OFR).

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Figures

Figure 1
Figure 1
Flowchart of the patient selection out of the DATA study. CIOFF, chemotherapy‐induced ovarian function failure. [Color figure can be viewed at wileyonlinelibrary.com]
Figure 2
Figure 2
Survival curves for patients with chemotherapy‐induced ovarian function failure (CIOFF) versus definitely postmenopausal women. (a) Disease‐free survival, (b) distant recurrence‐free survival and (c) overall survival. The adjusted hazard ratios were corrected for tumor size, nodal status, tumor grade, and hormone receptor status.
Figure 3
Figure 3
Residual survival curves for chemotherapy‐induced ovarian function failure (CIOFF) patients experiencing ovarian function recovery (OFR) in the first year after randomization versus CIOFF patients who did not experience OFR. (a) Disease‐free survival, (b) distant recurrence‐free survival, and (c) overall survival. These panels show the residual survival curves from the 12‐month landmark analyses of the effect of OFR on survival. The adjusted hazard ratios were corrected for tumor size, nodal status, tumor grade, and hormone receptor status.

References

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