Validation of the Prognostic Performance of Breast Cancer Index in Hormone Receptor–Positive Postmenopausal Breast Cancer Patients in the TEAM Trial

Author:

Bartlett John M.S.1ORCID,Xu Keying2ORCID,Wong Jenna3ORCID,Pond Gregory4ORCID,Zhang Yi3ORCID,Spears Melanie25ORCID,Salunga Ranelle3ORCID,Mallon Elizabeth6ORCID,Taylor Karen J.1ORCID,Hasenburg Annette7ORCID,Markopoulos Christos8ORCID,Dirix Luc9ORCID,van de Velde Cornelis J.H.10ORCID,Rea Daniel11ORCID,Schnabel Catherine A.3ORCID,Treuner Kai3ORCID,Bayani Jane25ORCID

Affiliation:

1. 1Cancer Research UK Scotland Centre, University of Edinburgh, Edinburgh, United Kingdom.

2. 2Diagnostic Development, Ontario Institute for Cancer Research, Toronto, Ontario, Canada.

3. 3Biotheranostics, A Hologic Company, San Diego, California.

4. 4Department of Biostatistics, McMaster University, Hamilton, Ontario.

5. 5Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario.

6. 6Department of Pathology, Glasgow, United Kingdom.

7. 7Department of Gynecology and Obstetrics, University Center Mainz, Mainz, Germany.

8. 8National and Kapodistrian University of Athens, Medical School, Athens, Greece.

9. 9St. Augustinus Hospital, Antwerp, Belgium.

10. 10Leiden University Medical Center, Leiden, the Netherlands.

11. 11Cancer Research UK Clinical Trials Unit, University of Birmingham, Birmingham, United Kingdom.

Abstract

Abstract Purpose: Patients with early-stage hormone receptor–positive (HR+) breast cancer face a prolonged risk of recurrence even after adjuvant endocrine therapy. The Breast Cancer Index (BCI) is significantly prognostic for overall (0–10 years) and late (5–10 years) distant recurrence (DR) risk in N0 and N1 patients. Here, BCI prognostic performance was evaluated in HR+ postmenopausal women from the Tamoxifen and Exemestane Adjuvant Multinational (TEAM) trial. Experimental Design: 3,544 patients were included in the analysis (N = 1,519 N0, N = 2,025 N+). BCI risk groups were calculated using pre-specified cutoff points. Kaplan–Meier analyses and log-rank tests were used to assess the prognostic significance of BCI risk groups based on DR. Hazard ratios (HR) and confidence intervals (CI) were calculated using Cox models with and without clinical covariates. Results: For overall 10-year DR, BCI was significantly prognostic in Ni0 (N = 1,196) and N1 (N = 1,234) patients who did not receive prior chemotherapy (P < 0.001). In patients who were DR-free for 5 years, 10-year late DR rates for low- and high-risk groups were 5.4% and 9.3% (N0 cohort, N = 1,285) and 4.8% and 12.2% (N1 cohort, N = 1,625) with multivariate HRs of 2.25 (95% CI, 1.30–3.88; P = 0.004) and 2.67 (95% CI, 1.53–4.63; P < 0.001), respectively. Late DR performance was substantially improved using previously optimized cutoff points, identifying BCI low-risk groups with even lower 10-year late DR rates of 3.8% and 2.7% in N0 and N1 patients, respectively. Conclusions: The TEAM trial represents the largest prognostic validation study for BCI to date and provides a more representative assessment of late DR risk to guide individualized treatment decision-making for HR+ patients with early-stage breast cancer.

Publisher

American Association for Cancer Research (AACR)

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