Abstract CT237: A randomized phase 2 non-inferiority trial of (Z)-endoxifen + goserelin and exemestane + goserelin as neoadjuvant treatment for premenopausal women with ER+/HER2- breast cancer (EVANGELINE)
Abstract Background: Endocrine therapy (ET) with aromatase inhibitors (AI) plus ovarian function suppression (OFS) is standard for premenopausal women with ER+/HER2- breast cancer. However, many premenopausal women are intolerant of AI + OFS, leaving tamoxifen (with or without OFS) as their only option. Extensive studies have demonstrated that premenopausal women treated with neoadjuvant ET whose tumors exhibit Ki-67 ≤ 10% following 4 weeks of therapy (defined as endocrine sensitive disease (ESD)) achieve 5-year distant disease-free survival > 96%. Problematically, only 41% of patients reach this ESD threshold with tamoxifen compared to 78% with AI+OFS (Nitz JCO 2022). (Z)-endoxifen (ENDX) is a potent selective estrogen receptor modulator (SERM) that inhibits ERα at plasma concentrations of 3-5 ng/ml and dually targets PKCβ1, a suspected oncogene in breast tumors, at concentrations ≥ 500 ng/ml. We therefore developed the EVANGELINE study (NCT05607004) is an open label, randomized neoadjuvant phase II study that includes a pharmacokinetic (PK) Run-in, aiming to evaluate whether ENDX +/- goserelin is non-inferior to exemestane plus goserelin with respect to ESD rate. Following the completed PK run-in portion of the study, where 40mg/day or 80mg/day ENDX were assessed, the 40 mg/day dose was selected for further evaluation in the second part of the trial. The second part is comprised of a randomized treatment cohort, for patients with a Ki-67% >10% at preregistration randomized to either 40mg (Z)-endoxifen + goserelin or exemestane + goserelin neoadjuvant treatment and a Single Arm Treatment Cohort for patients who have a Ki-67 ≤ 10% at pre-registration assigned to 40mg/day (Z)-endoxifen monotherapy neoadjuvant treatment. Methods: To investigate ENDX further in premenopausal women, a multicenter study in the United States, was designed(EVANGELINE; NCT05607004). This phase 2, open-label, randomized, neoadjuvant trial includes a PK run-in phase designed to assess whether the 4-week ESD rate with (Z)-endoxifen + goserelin is non-inferior to that of exemestane + goserelin in premenopausal women with Stage IIA or IIB ER+/HER2- breast cancer with diagnostic Ki67 > 10%. Additionally, a single arm Phase 2, open-label neoadjuvant Cohort was designed to assess the 4-week ESD rate with ENDX monotherapy in premenopausal women with Stage IIA or IIB ER+/HER2- BC with diagnostic Ki67 ≤10%. Subjects will undergo neoadjuvant treatment for six months before receiving surgical treatment in the involved breast. This study will additionally assess safety, tolerability, response rates, surgical outcomes, and monitor disease progression. Comprehensive biomarker evaluations will be conducted using paired tumor biopsies and blood samples collected at baseline and week four, as well as 6 month surgical specimens. Enrollment in the PK run-in phase (n-22) was completed in Fall 2024 with the second portion of the trial slated to begin early in 2025. Citation Format: Matthew P. Goetz, Vera J. Suman, Claudia Lopez, Hayley Erickson, Lonnissa Nguyen, Sandra S. Hammer, Lida Mina, Pooja Advani, Roberto Leon-Ferre, Karthik Giridhar, Felipe Batalini, Daniel Flora, Jason M. Jones, Nusayba A. Bagegni, Katie N. Hunt, Mara Piltin, Amy Degnim, James N. Ingle, Judy C. Boughey, Sarah A. Buhrow, Joel M. Reid, Matthew Schellenberg, John R. Hawse, Steven C. Quay. A randomized phase 2 non-inferiority trial of (Z)-endoxifen + goserelin and exemestane + goserelin as neoadjuvant treatment for premenopausal women with ER+/HER2- breast cancer (EVANGELINE) [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_2):Abstract nr CT237.
Authors
- Steven C. Quay (ORCID: https://orcid.org/0000-0002-0363-7651)
- Matthew J. Schellenberg (ORCID: https://orcid.org/0000-0001-7036-5943)
- Matthew P. Goetz (ORCID: https://orcid.org/0000-0002-4383-270X)
- Pooja Prem Advani (ORCID: https://orcid.org/0009-0007-5470-3149)
- Sarah A. Buhrow (ORCID: https://orcid.org/0009-0003-5723-5409)
- Amy C. Degnim (ORCID: https://orcid.org/0000-0002-2303-4946)
- Daniel Flora (ORCID: https://orcid.org/0000-0002-0762-5041)
- Felipe Batalini (ORCID: https://orcid.org/0000-0003-3354-308X)
- Joel M. Reid (ORCID: https://orcid.org/0000-0003-2872-3123)
- Jason M. Jones (ORCID: https://orcid.org/0000-0001-6460-8427)
- Judy C. Boughey (ORCID: https://orcid.org/0000-0003-3820-3228)
- John R. Hawse (ORCID: https://orcid.org/0000-0003-3406-470X)
- Katie N. Hunt (ORCID: https://orcid.org/0000-0003-2889-3528)
- Nusayba Ali Bagegni (ORCID: https://orcid.org/0000-0001-9322-2451)
- Roberto A. Leon‐Ferre (ORCID: https://orcid.org/0000-0003-0594-4441)
- Lida A. Mina (ORCID: https://orcid.org/0000-0003-2606-9922)
- Mara A. Piltin (ORCID: https://orcid.org/0000-0002-0863-8258)
- Clàudia López
- Vera J. Suman (ORCID: https://orcid.org/0000-0002-9640-5189)
- James N. Ingle (ORCID: https://orcid.org/0000-0003-1257-7731)
- Karthik V. Giridhar (ORCID: https://orcid.org/0000-0003-4640-9197)
- Lonnissa Nguyen
- H. Erickson
- Sandra S. Hammer (ORCID: https://orcid.org/0009-0003-7760-4582)
Institutions
- Mayo Clinic (US)
- Avera Health (US)
- St. Elizabeth Healthcare (US)
- Aptevo Therapeutics (United states) (US)
- Mayo Clinic in Arizona (US)
- Atossa Therapeutics (United States) (US)
- Mayo Clinic in Florida (US)
Publication Details
- Journal
- Cancer Research
- Published
- 2025-04-25
- DOI
- https://doi.org/10.1158/1538-7445.am2025-ct237
- Primary Topic
- Advanced Breast Cancer Therapies
- Type
- article
- Field-Weighted Citation Impact
- 0.00