Abstract 364P
Background
Endocrine therapy plus a CDK4/6 inhibitor (ET+CDK4/6i) is the mainstay in 1st-line ER+, HER2- mBC; however, tumors often develop resistance. In EMERALD, single-agent elacestrant was associated with significantly prolonged PFS with manageable safety vs standard-of-care (SOC) ET in pts with ER+, HER2-, ESR1-mut mBC previously treated with ET+CDK4/6i (HR = 0.55; 95% CI, 0.39-0.77; P = 0.0005) (Bidard, 2022), resulting in the first oral SERD approved. The rationale for ELECTRA (NCT05386108) is to combine elacestrant + abemaciclib to overcome additional resistance mechanisms, improve efficacy, and enable an all-oral treatment option that can delay chemotherapy-based regimens, including ADCs.
Methods
Eligible pts have ER+, HER2- mBC. For phase 1b, brain mets are not required. For phase 2, the presence of ≥1 active and measurable brain mets per RECIST v1.1 is required. In the mBC setting, pts must have previously received ≥1 ET, ≤2 chemotherapy regimens, and 0-2 prior CDK4/6i (excluding abemaciclib). Phase 1b primary objective is to determine the recommended phase 2 dose (RP2D) of elacestrant + abemaciclib. Phase 2 will evaluate the efficacy and safety of the combination in pts with brain mets as both compounds have also been shown to cross the BBB (Conlan, 2020; Tolaney, 2020).
Results
As of April 2024, 27 pts were enrolled in phase 1b, none with brain mets. The most common all-grade AEs at the selected RP2D (elacestrant 345 mg QD + abemaciclib 150 mg BID) are shown in Table. No Grade 4 AEs or Grade 3 diarrhea were observed. Updated safety will be reported. Table: 364P
Treatment-emergent adverse events (≥35%) at the RP2D
Elacestrant 345 mg QD + Abemaciclib 150 mg BID; n=12 | ||
Preferred term, n (%) | All Grade | Grade 3 |
Diarrhea | 10 (83) | 0 |
Neutropenia/neutrophil count decreased - Related to abemaciclib only - Related to elacestrant + abemaciclib | 8 (67)5 (42)3 (25) | 7 (58)5 (42)2 (17) |
Nausea | 7 (58) | 1 (8) |
Anemia | 5 (42) | 1 (8) |
Conclusions
The elacestrant + abemaciclib combination shows a manageable/predictable safety profile and favorable efficacy. Elacestrant has the potential to become the ET backbone for combination regimens. The Phase 2 portion of the study is currently enrolling.
Clinical trial identification
NCT05386108.
Editorial acknowledgement
Editorial assistance was provided by Mark Phillips, PharmD, MBA of The Phillips Group Oncology Communications, Inc.
Legal entity responsible for the study
Menarini Group.
Funding
Menarini Group.
Disclosure
E.M. Ciruelos: Financial Interests, Personal, Other, Speakers Bureau. Educational activities: Roche; Financial Interests, Personal, Invited Speaker, Symposia and Educational activities: Roche; Financial Interests, Personal, Advisory Board, Non-permanent advisor: Roche, Lilly, Novartis, Pfizer, Daiichi Sankyo, MSD; Financial Interests, Personal, Invited Speaker, Symposia and Education: Lilly; Financial Interests, Personal, Invited Speaker, Educational activities: Pfizer; Financial Interests, Personal, Advisory Board, Non-permanent advisor, Travel accommodation: AstraZeneca; Financial Interests, Personal, Other, Advisory Board: Gilead; Financial Interests, Personal, Other, Advisory Board, Invited speaker: Seagen; Financial Interests, Institutional, Funding, PI for Patricia 2 trial (sponsor: SOLTI Group): Pfizer; Financial Interests, Institutional, Funding, PI for Prometeo 2 trial (sponsor: SOLTI Group): Pfizer; Financial Interests, Institutional, Funding, PI for TATEN trial (sponsor: SOLTI Group): MSD; Financial Interests, Institutional, Funding, PI for ATREZZO trial (sponsor: SOLTI Group): Roche; Non-Financial Interests, Member of Board of Directors, Non-profit organization dedicated to breast cancer research: SOLTI Cooperative Group; Non-Financial Interests, Advisory Role, Scientific Evaluator at ISCIII (Spanish Government Academic Research Platform): Instituto de Salud Carlos III. E.P. Hamilton: Financial Interests, Institutional, Other, Consulting/Advisory Role: Genentech/Roche, Novartis, Lilly, Pfizer, Mersana, Olema Pharmaceuticals, Stemline Therapeutics, AstraZeneca, Daiichi Sankyo, Ellipses Pharma, Tubulis, Verascity Science, Theratechnologies; Financial Interests, Institutional, Other, Consulting: Accutar Biotechnology, Entos, Fosun Pharma, Gilead Sciences, Jazz Pharmaceuticals, Jefferies LLC, Medical Pharma Services, Tempus Labs, Zentalis Pharmaceuticals; Financial Interests, Institutional, Research Grant: Oncomed, Genentech/Roche, Zymeworks, Rgenix, Arqule, Clovis, Millennium, Acerta Pharma, Sermonix Pharmaceuticals, Black Diamond, Karyopharm, Curis, Syndax, Novartis, Boehringer Ingelheim, Immunomedics, FujiFilm, Taiho, Deciphera, Molecular Templates, Dana Farber Cancer Inst, Hutchinson MediPharma, MedImmune, Seagen, Compugen, TapImmune, Lilly, Pfizer, H3 Biomedicine, Merus, Regeneron, Arvinas, StemCentRx, Verastem, eFFECTOR Therapeutics, CytomX, InventisBio, Lycera, Mersana, Radius Health, Abbvie, Nucana, Leap Therapeutics, Zenith Epigenetics, Harpoon, Orinove, AstraZeneca, Tesaro, Macrogenics, EMD Serono, Daiichi Sankyo, Syros, Sutro, G1 Therapeutics, PharmaMar, Olema, Immunogen, Plexxicon, Amgen, Akesobio Australia, Shattuck Labs, ADC Therapeutics, Aravive, Atlas MedX, Ellipses Pharma, Incyte, Jacobio, Mabspace Biosciences, ORIC Pharmaceuticals, Pieris Pharmaceuticals, Pionyr Immunotherapeutics, Repertoire Immune Medicine, Treadwell Therapeutics, Accutar Biotechnology, Artios, BeiGene, Bliss BioPharmaceuticals, Cascadian Therapeutics, Context Therapeutics, Cullinan, Dantari, Duality Biologics, Elucida Oncology, Infinity Pharmaceuticals, K-Group Beta, Kind Pharmaceuticals, Loxo Oncology, Oncothyreon, Orum Therapeutics, Prelude Therapeutics, Profound Bio, Relay Therapeutics, Tolmar, Torque Therapeutics; Financial Interests, Institutional, Local PI: Bristol-Myers Squibb, Eisai, Fochon Pharmaceuticals, Gilead Sciences, Inspirna, Myriad Genetic Laboratories, Silverback Therapeutics, Stemline Therapeutics. S. Kim: Financial Interests, Personal, Advisory Board: Novartis, AstraZeneca, Lilly, DaeHwa Pharma, ISU Abx, Daiich-Sankyo, BeiGene, Samsung Bioepics, OBI pharma; Financial Interests, Personal, Invited Speaker: Legochem Bioscience; Financial Interests, Personal, Ownership Interest: Genopeaks; Financial Interests, Institutional, Research Grant: Novartis, Sanofi-Genzyme, DongKook Pharm Co. E. Segui Solis: Financial Interests, Personal, Invited Speaker: Novartis, Veracyte, Pfizer, Daiichi Sankyo, Eisai; Financial Interests, Personal, Advisory Board: Pfizer, Seagen; Financial Interests, Personal, Full or part-time Employment: SOLTI; Financial Interests, Personal, Research Grant: Amgen. J. Á. García Saenz: Financial Interests, Personal, Speaker, Consultant, Advisor: Novartis, AstraZeneca, Lilly, Daiichi Sankyo/AstraZeneca, Gilead Sciences, Seattle Genetics; Financial Interests, Personal, Speaker’s Bureau: Novartis; Financial Interests, Institutional, Research Funding: AstraZeneca; Financial Interests, Personal, Other, Travel: Roche, Novartis. A. Di Sanzo: Financial Interests, Personal, Full or part-time Employment: Menarini Group. M. Domínguez Lizarbe: Financial Interests, Personal, Full or part-time Employment: Menarini Group. T. Wasserman: Financial Interests, Personal, Full or part-time Employment: Menarini Group. K.P. Theall: Financial Interests, Personal, Full or part-time Employment: Menarini Group. All other authors have declared no conflicts of interest.
Resources from the same session
311P - Optimizing breast cancer staging: Redefining tumor size classification using big data analytics
Presenter: Bin Feng
Session: Poster session 14
312P - Early detection of metastatic disease in asymptomatic early-stage breast cancer patients using imaging: A cross-sectional analytic study at a tertiary hospital
Presenter: John kelvin Lalusis
Session: Poster session 14
313P - A longitudinal follow-up study on the prognosis of patients with breast cancer with delayed diagnosis during the COVID-19 pandemic
Presenter: Jae Pak Yi
Session: Poster session 14
314P - The impact of changes in tumor mutational landscape during neoadjuvant therapy on tumor-informed ctDNA testing in breast cancer patients
Presenter: Mark Magbanua
Session: Poster session 14
315P - Long-term tamoxifen benefit in pre- and postmenopausal patients of high and low risk with luminal A and B breast cancer
Presenter: Oscar Danielsson
Session: Poster session 14
316P - Differential long-term benefit of 2-year adjuvant tamoxifen therapy for luminal-type breast cancer: Insights from a 20-year follow-up analysis of the STO trials
Presenter: Magdalena Rios Romero
Session: Poster session 14
317TiP - A randomized, multicenter, open-label phase II neoadjuvant study to evaluate the safety and efficacy of HER2-ADC disitamab vedotin in combination toripalimab or sequence chemotherapy in participants with HR-negative, HER2 low-expressing breast cancer
Presenter: Zhimin Shao
Session: Poster session 14
318TiP - Neoadjuvant trastuzumab, pertuzumab and tucatinib without chemotherapy in stage II-III HER2-positive breast cancer: The TRAIN-4 study
Presenter: Fleur Louis
Session: Poster session 14
319TiP - NeoBREASTIM: A phase II study of atezolizumab plus RP1 oncolytic immunotherapy in the neoadjuvant setting of triple-negative breast cancer (TNBC)
Presenter: Etienne Bastien
Session: Poster session 14
321P - Sentinel lymph node biopsy in clinical T3-4c breast cancer: A retrospective multicenter cohort study
Presenter: Yasuaki Sagara
Session: Poster session 14