Imlunestrant, an Oral Selective Estrogen Receptor Degrader, as Monotherapy and in Combination With Targeted Therapy in Estrogen Receptor–Positive, Human Epidermal Growth Factor Receptor 2–Negative Advanced Breast Cancer: Phase Ia/Ib EMBER Study

Imlunestrant, as monotherapy or in combination with targeted therapy, had a manageable safety profile with evidence of preliminary antitumor activity in ER+/HER2- ABC.

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Institutions

Publication Details

Journal
Journal of Clinical Oncology
Published
2024-09-06
DOI
https://doi.org/10.1200/jco.23.02733
Citations
31
Primary Topic
Advanced Breast Cancer Therapies
Type
article
Field-Weighted Citation Impact
12.99

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article

Imlunestrant, an Oral Selective Estrogen Receptor Degrader, as Monotherapy and in Combination With Targeted Therapy in Estrogen Receptor–Positive, Human Epidermal Growth Factor Receptor 2–Negative Advanced Breast Cancer: Phase Ia/Ib EMBER Study

Erika Hamilton, J. Thaddeus Beck, Manali Ajay Bhave, Timothy Larson et al.
31 citations
Journal of Clinical Oncology
Advanced Breast Cancer Therapies
12.99
article

Imlunestrant, an Oral Selective Estrogen Receptor Degrader, as Monotherapy and in Combination With Targeted Therapy in Estrogen Receptor–Positive, Human Epidermal Growth Factor Receptor 2–Negative Advanced Breast Cancer: Phase Ia/Ib EMBER Study

Erika Hamilton, J. Thaddeus Beck, Manali Ajay Bhave, Timothy Larson, Patrick Neven, Yen‐Shen Lu, Muralidhar Beeram, Ajay Dhakal, Sarah Sammons, Peter A. Kaufman, Jean‐Yves Pierga, Roohi Ismail‐Khan, Bastien Nguyen, Kan Yonemori, Yolanda Jerez, Sung‐Bae Kim, Joohyuk Sohn, Aditya Bardia, Cynthia X. Ma, Shawn T. Estrem, Luís Manso, Komal L. Jhaveri, Kathleen Harnden, Kostandinos Sideras, Rinath M. Jeselsohn, Eunice Yuen, Seock‐Ah Im, Jessica J. Tao, Philippe Aftimos, Cynthia R. Osborne, Vanessa Rodrik-Outmezguine, Cristina Saura, Elgene Lim, Lillian M. Smyth, Yujia Li, Hwei-Chung Wang, Francesca Bacchion, Ritesh Parajuli
article en
31 citations

Abstract

Imlunestrant, as monotherapy or in combination with targeted therapy, had a manageable safety profile with evidence of preliminary antitumor activity in ER+/HER2- ABC.

Journal of Clinical OncologyVol. 42(35)
University of Vermont (US), Ulsan College (KR), McKesson (United States) (US), Université Libre de Bruxelles (BE), Memorial Sloan Kettering Cancer Center (US), Garvan Institute of Medical Research (AU), Johns Hopkins University (US), Emory University (US), Eli Lilly (United States) (US), China Medical University (TW), Yonsei University (KR), University of California, Irvine (US), Washington University in St. Louis (US), Université Paris Cité (FR), Cornell University (US), Severance Hospital (KR), Texas Oncology (US), Universitair Ziekenhuis Leuven (BE), Jacksonville College (US), Asan Medical Center (KR), Institut Jules Bordet (BE), WinnMed (US), Seoul National University Hospital (KR), University of Rochester Medical Center (US), Hospital General Universitario Gregorio Marañón (ES), UNSW Sydney (AU), University of Ulsan (KR), Massachusetts General Hospital (US), Virginia Cancer Institute (US), Sarah Cannon (US), Hospital Universitario 12 De Octubre (ES), Highlands Oncology Group (US), Dana-Farber Cancer Institute (US), South Texas Accelerated Research Therapeutics (US), St Vincent's Clinic (AU), Duke Medical Center (US), China Medical University Hospital (TW), Vall d'Hebron Hospital Universitari (ES), National Taiwan University Hospital (TW), Tennessee Oncology (US), Center for Health Care Services (US), Mayo Clinic in Florida (US), The US Oncology Network (US), Tokyo National Hospital (JP), Centro de Investigación Biomédica en Red de Cáncer (ES), Sidney Kimmel Comprehensive Cancer Center (US), Minnesota Oncology (US), Vall d'Hebron Institute of Oncology (ES), Institut Curie (FR)
Eli Lilly and Company, Memorial Sloan-Kettering Cancer Center
Good health and well-being
Openalex Percentile: Top 1%
Advanced Breast Cancer Therapies
12.99
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