Abstract

To assess the prognostic value of the PAM50 risk-of-recurrence (ROR) score on late distant recurrence (beyond 5 years after diagnosis and treatment) in a large cohort of postmenopausal, endocrine-responsive breast cancer patients. The PAM50 assay was performed on formalin-fixed paraffin-embedded whole-tumor sections of patients who had been enrolled in the Austrian Breast and Colorectal Cancer Study Group Trial 8 (ABCSG-8). RNA expression levels of the PAM50 genes were determined centrally using the nCounter Dx Analysis System. Late distant recurrence-free survival (DRFS) was analyzed using Cox models adjusted for clinical and pathologic parameters. PAM50 analysis was successfully performed in 1,246 ABCSG-8 patients. PAM50 ROR score and ROR-based risk groups provided significant additional prognostic information with respect to late DRFS compared with a combined score of clinical factors alone (ROR score: ΔLRχ(2) 15.32, P < 0.001; ROR-based risk groups: ΔLRχ(2) 14.83, P < 0.001). Between years 5 and 15, we observed an absolute risk of distant recurrence of 2.4% in the low ROR-based risk group, as compared with 17.5% in the high ROR-based risk group. The DRFS differences according to the PAM50 ROR score were observed for both node-positive and node-negative disease. PAM50 ROR score and ROR-based risk groups can differentiate patients with breast cancer with respect to their risk for late distant recurrence beyond what can be achieved with established clinicopathologic risk factors.

Highlights

  • More than two-thirds of breast cancers express estrogen receptor (ER) and/or progesterone receptor (PgR; ref. 1).These patients are candidates for treatment with drugs targeting ER signaling either by interfering with ligand binding, blockade of estrogen biosynthesis, or ER downregulation

  • Between years 5 and 15, we observed an absolute risk of distant recurrence of 2.4% in the low ROR-based risk group, as compared with 17.5% in the high ROR-based risk group

  • The distant recurrence-free survival (DRFS) differences according to the PAM50 ROR score were observed for both node-positive and node-negative disease

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Summary

Introduction

More than two-thirds of breast cancers express estrogen receptor (ER) and/or progesterone receptor These patients are candidates for treatment with drugs targeting ER signaling either by interfering with ligand binding (tamoxifen), blockade of estrogen biosynthesis (aromatase inhibitors or gonadotropin-releasing hormone analogs), or ER downregulation (fulvestrant). Adjuvant treatment with tamoxifen reduces the risk-of-recurrence (ROR) in patients with ER-positive breast cancer over all time periods by 39% [1]. 50% of recurrences in ER-positive disease will occur after the first 5 years beyond initial diagnosis and tamoxifen treatment [1]. Mortality and recurrence risk vary over time according to molecular and clinical risk factors. In contrast with ERnegative tumors, which usually develop metastases early (mostly within 5 years) after initial diagnosis and treatment, the annual recurrence rates of ER-positive breast cancers are

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