Time-varying hazard rates reveal patterns of progression in HR+/HER2– metastatic breast cancer: Towards risk-adapted monitoring

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Authors: Linda Cucciniello, Fabiola Giudici, Lorenzo Foffano, Alessandra Franzoni, Brenno Pastò, Elisabetta Molteni, Serena Della Rossa, Gaetano Pascoletti, Simon Spazzapan, Lorena Musco, Gabriele Di Giustino, Lucia Da Ros
+9 more Riccardo Vida, Elena Poletto, Elena Nascimbeni, Marta Bonotto, Alessandro Marco Minisini, Barbara Belletti, Giuseppe Damante, Lorenzo Gerratana, Fabio Puglisi
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References: 30

Abstract

BACKGROUND: optimal imaging intervals for patients with hormone receptor-positive/HER2-negative metastatic breast cancer (MBC) remains undefined. Aim of this study was to analyze the temporal patterns of disease progression to identify high risk subgroups that may benefit from intensified monitoring. METHODS: we analyzed 149 hormone receptor-positive/HER2-negative MBC patients prospectively enrolled in the MAGNETIC.1 trial (NCT05814224) and treated with first line endocrine therapy. Hazard rates (HR) for disease progression were determined according to clinico-pathological and liquid biopsy features. RESULTS: in the overall population, two distinct progression-risk peaks emerged at 2-3 months (32.9/1000 person-months) and at 24 months (28.0/1000). Higher risk of progression was observed in lobular carcinoma (61.1) [HR 61.12 per 1000 person month (pm)], progesterone receptor-negative status (HR 39.07), fulvestrant-based treatment (HR 46.88), liver metastases (HR 59.00), and presence of ≥ 3 metastatic sites (HR 40.10). CONCLUSIONS: Hazard distribution in hormone receptor-positive/HER2-negative MBC is biphasic and modulated by readily available clinical variables. High-risk subgroups may benefit from intensified radiologic and liquid-biopsy surveillance during the first three months and around two years after treatment start.

Fields of Study & Subjects

Advanced Breast Cancer Therapies Breast Cancer Treatment Studies Cancer-related Molecular Pathways

Publication details

Journal / source
Translational Oncology
Volume
72
Pages
102960–102960
Publication date
28 July 2026
Language
EN