ALTERNATE: Neoadjuvant endocrine treatment (NET) approaches for clinical stage II or III estrogen receptor-positive HER2-negative breast cancer (ER+ HER2- BC) in postmenopausal (PM) women: Alliance A011106.

Authors

null

Cynthia X. Ma

Washington University School of Medicine in St. Louis, St. Louis, MO

Cynthia X. Ma , Vera J. Suman , A. Marilyn Leitch , Souzan Sanati , Kiran R. Vij , Gary Walter Unzeitig , Jeremy Hoog , Mark Watson , Olwen Mary Hahn , J. Michael Guenther , Abigail Suzanne Caudle , Travis Dockter , Larissa A. Korde , Anna Weiss , Kelly Hunt , Clifford A. Hudis , Eric P. Winer , Ann H. Partridge , Lisa A. Carey , Matthew James Ellis

Organizations

Washington University School of Medicine in St. Louis, St. Louis, MO, Mayo Clinic, Rochester, MN, The University of Texas Southwestern Medical Center, Dallas, TX, Cedars Sanai Medical Center, Los Angeles, CA, Washington University in St. Louis School of Medicine, St. Louis, MO, Laredo Breast Care, Laredo, TX, Washington University School of Medicine, St. Louis, MO, University of Chicago Medical Center, Chicago, IL, St. Elizabeth Healthcare, Edgewood, KY, The University of Texas MD Anderson Cancer Center, Houston, TX, Mayo Clinic, Department of Biostatistics, Rochester, MN, Clinical Investigations Branch, National Cancer Institute, Bethesda, MD, Dana-Farber Cancer Institute, Bethesda, MD, Memorial Sloan Kettering Cancer Center, New York, NY, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, Dana-Farber Cancer Institute, Boston, MA, University of North Carolina, Chapel Hill, NC, Lester and Sue Smith Breast Center, Baylor Clinic, Baylor College of Medicine, Houston, TX

Research Funding

Other Government Agency
U10CA180821, U10CA180882, U24CA196171; Alliance Foundation, NCI Biomarker, Imaging and Quality of Life Studies Funding Program (BIQSFP), Breast Cancer Research Foundation, Genentech, AstraZeneca, https://acknowledgments.alliancefound.org

Background: For PM patients (pts) with locally advanced ER+ HER2- BC, NET improves breast conservation surgery (BCS) rates, and modified preoperative endocrine prognostic index (mPEPI) 0, defined as pT1-2 pN0 Ki67< 2.7%, or pathologic complete response (pCR: no invasive disease in breast or lymph node) is associated with low risk of recurrence without adjuvant chemotherapy (CT). The ALTERNATE trial was initiated to assess if the endocrine-sensitive disease rate (ESDR: number of mPEPI 0 pts/number of eligible pts initiating NET) with fulvestrant (F) or F+anastrozole (A) is improved relative to A alone (reported here) and if the 5-year (yr) recurrence-free survival (RFS) rate for pts with mPEPI 0 on A alone without CT is ≥ 95% (awaits further follow-up). Methods: PM pts with clinical stage II/III ER+ HER2- BC were randomized 1:1:1 to 1 mg A po daily, 500 mg F IM every 4 week (wk)s after loading dose, or A+F for 6 months. Ki67 was tested centrally on biopsies acquired prior to NET, wk 4, wk 12 and at surgery. Pts with Ki67 >10% at wk 4 or 12 were recommended to go off protocol-directed ET and switch to CT. Pts with mPEPI 0 at surgery were recommended to continue assigned ET for 1.5 yrs followed by A for a total of 5 yrs ET (and not to receive CT). The primary endpoint of the neoadjuvant phase was ESDR. ESDR of each F arm was compared to that of the A alone arm. With 425 pts per arm, a one-tailed alpha = 0.025 chi-square test of two independent proportions has 84% power to detect an increase of ≥10% in ESDR for F or F+A compared to the A arm, assuming ESDR ≤30% in A. Results: 1362 pts (A 452; F 454; A+F 456) were enrolled Feb 2014 to Nov 2018. 63 pts were excluded (did not start NET). Of the remaining 1299 pts (A 434; F 431, A+F 434), 42% were cN1-3 and 73% were considered candidates for BCS. ESDR was 18.6% (95%CI: 15.1-22.7%) with A, 22.7% (95%CI: 18.9-27.0%) with F, and 20.5% (95%CI: 16.8-24.6%) with A+F. No significant difference in ESDR was found between A and F (p=0.15) or A and A+F (p=0.55). Among the 825 pts with wk 4 Ki67 < 10% who completed NET and surgery, ESDR and the BCS rate were 27.7% and 70.3% with A; 29.6% and 68.1% with F, and 26.8% and 69.9% with A+F, respectively. Conclusion: Neither F nor F+A significantly improved ESDR compared to A alone in PM pts with locally advanced ER+ HER2- BC. RFS data are awaited. Support: U10CA180821, U10CA180882, U24CA196171, https://acknowledgments.alliancefound.org; NCI BIQSFP, BCRF, Genentech, AstraZeneca. Clinical trial information: NCT01953588.

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Abstract Details

Meeting

2020 ASCO Virtual Scientific Program

Session Type

Oral Abstract Session

Session Title

Breast Cancer—Local/Regional/Adjuvant

Track

Breast Cancer

Sub Track

Neoadjuvant Therapy

Clinical Trial Registration Number

NCT01953588

Citation

J Clin Oncol 38: 2020 (suppl; abstr 504)

DOI

10.1200/JCO.2020.38.15_suppl.504

Abstract #

504

Abstract Disclosures