A Randomized Trial of Fulvestrant, Everolimus, and Anastrozole for the Front-line Treatment of Patients with Advanced Hormone Receptor–positive Breast Cancer, SWOG S1222

富维斯特朗 阿那曲唑 依维莫司 医学 肿瘤科 内科学 乳腺癌 转移性乳腺癌 癌症 来曲唑 三苯氧胺
作者
Halle C. F. Moore,William E. Barlow,George Somlo,Julie R. Gralow,Anne F. Schott,Daniel F. Hayes,Peter Kühn,James Hicks,Lisa Welter,Philip A. Dy,Christina Yeon,Alison Conlin,Ernie Balcueva,Danika Lew,Debasish Tripathy,Lajos Pusztai,Gabriel N. Hortobágyi
出处
期刊:Clinical Cancer Research [American Association for Cancer Research]
卷期号:28 (4): 611-617 被引量:2
标识
DOI:10.1158/1078-0432.ccr-21-3131
摘要

Metastatic hormone receptor (HR)-positive, HER2-negative breast cancer is an important cause of cancer mortality. Endocrine treatment with or without additional targeted therapies has been the mainstay of treatment. This trial was designed to evaluate the combination of fulvestrant plus everolimus versus fulvestrant, everolimus, and anastrozole compared with fulvestrant alone in the first-line treatment of advanced HR-positive, HER2-negative breast cancer.This randomized placebo-controlled trial included postmenopausal women with HR-positive, HER2-negative advanced breast cancer who had received no prior systemic therapy for metastatic disease. Participants were randomized to one of three treatment arms and the primary outcome was progression-free survival (PFS), comparing combinations of fulvestrant and everolimus with or without anastrozole with fulvestrant alone. Circulating tumor cells (CTC), as measured with two different methods, and circulating tumor DNA (ctDNA) were evaluated serially prior to treatment and the beginning of the second cycle of therapy.Due in part to changes in clinical practice, the study was closed after accruing only 37 participants. There was no evidence that everolimus-containing combination treatment improved PFS or overall survival relative to fulvestrant alone. When modeled continuously, an association was observed of baseline CTC and ctDNA with poorer survival.Although power of the study was limited, the findings were unable to support the routine use of everolimus combination endocrine therapy in the first-line treatment of advanced hormone-sensitive breast cancer. Prognostic impact of baseline ctDNA and copy-number variations in CTC was demonstrated.
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