The Phase II MutHER Study of Neratinib Alone and in Combination with Fulvestrant in HER2-Mutated, Non-amplified Metastatic Breast CancerNeratinib and Fulvestrant in HER2-Mutated Breast Cancer
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Ma, Cynthia X, et al. The Phase Ii Muther Study of Neratinib Alone and In Combination with Fulvestrant In Her2-mutated, Non-amplified Metastatic Breast Cancerneratinib and Fulvestrant In Her2-mutated Breast Cancer. American Association for Cancer Research (AACR), 2022. https://doi.org/10.17615/kd1v-9129APA
Ma, C., Luo, J., Freedman, R., Pluard, T., Nangia, J., Lu, J., Valdez Albini, F., Cobleigh, M., Jones, J., Lin, N., Winer, E., Marcom, P., Thomas, S., Anderson, J., Haas, B., Bucheit, L., Bryce, R., Lalani, A., Carey, L., Goetz, M., Gao, F., Kimmick, G., Pegram, M., Ellis, M., & Bose, R. (2022). The Phase II MutHER Study of Neratinib Alone and in Combination with Fulvestrant in HER2-Mutated, Non-amplified Metastatic Breast CancerNeratinib and Fulvestrant in HER2-Mutated Breast Cancer. American Association for Cancer Research (AACR). https://doi.org/10.17615/kd1v-9129Chicago
Ma, Cynthia X., Jingqin Luo, Rachel A Freedman, Timothy J Pluard, Julie R Nangia, Janice Lu, Frances Valdez Albini et al. 2022. The Phase Ii Muther Study of Neratinib Alone and In Combination with Fulvestrant In Her2-Mutated, Non-Amplified Metastatic Breast Cancerneratinib and Fulvestrant In Her2-Mutated Breast Cancer. American Association for Cancer Research (AACR). https://doi.org/10.17615/kd1v-9129- Creator
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Ma, Cynthia X.
- Other Affiliation: Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri
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Luo, Jingqin
- ORCID: https://orcid.org/0000-0003-2759-3072
- Other Affiliation: Siteman Cancer Center, St. Louis, Missouri
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Freedman, Rachel A.
- ORCID: https://orcid.org/0000-0003-0460-674X
- Other Affiliation: Dana-Farber Cancer Institute, Boston, Massachusetts
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Pluard, Timothy J.
- ORCID: https://orcid.org/0000-0002-3640-3077
- Other Affiliation: Saint Luke's Cancer Institute, Kansas City, Missouri
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Nangia, Julie R.
- ORCID: https://orcid.org/0000-0002-8326-2254
- Other Affiliation: Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas
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Lu, Janice
- Other Affiliation: University of Southern California, Los Angeles, California
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Valdez-Albini, Frances
- Other Affiliation: University of Miami, Coral Gables, Florida
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Cobleigh, Melody
- ORCID: https://orcid.org/0000-0001-6385-4693
- Other Affiliation: Rush University Medical Center, Chicago, Illinois
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Jones, Jason M.
- Other Affiliation: Avera Cancer Institute, Sioux Falls, South Dakota
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Lin, Nancy U.
- Other Affiliation: Dana-Farber Cancer Institute, Boston, Massachusetts
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Winer, Eric P.
- Other Affiliation: Dana-Farber Cancer Institute, Boston, Massachusetts
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Marcom, P. Kelly
- ORCID: https://orcid.org/0000-0001-5302-6368
- Other Affiliation: Duke Cancer Institute, Durham, North Carolina
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Thomas, Shana
- Other Affiliation: Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri
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Anderson, Jill
- Other Affiliation: Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri
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Haas, Brittney
- Other Affiliation: Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri
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Bucheit, Leslie
- ORCID: https://orcid.org/0000-0001-8826-0357
- Other Affiliation: Guardant Health Inc, Redwood City, California
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Bryce, Richard
- Other Affiliation: Puma Biotechnology, Los Angeles, California
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Lalani, Alshad S.
- ORCID: https://orcid.org/0000-0003-4891-9983
- Other Affiliation: Puma Biotechnology, Los Angeles, California
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Carey, Lisa A.
- ORCID: https://orcid.org/0000-0003-2388-4649
- University of North Carolina at Chapel Hill
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Goetz, Matthew P.
- ORCID: https://orcid.org/0000-0002-4383-270X
- Other Affiliation: Mayo Clinic, Rochester, Minnesota
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Gao, Feng
- ORCID: https://orcid.org/0000-0002-1425-1623
- Other Affiliation: Siteman Cancer Center, St. Louis, Missouri
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Kimmick, Gretchen
- ORCID: https://orcid.org/0000-0001-7096-9624
- Other Affiliation: Duke Cancer Institute, Durham, North Carolina
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Pegram, Mark D.
- Other Affiliation: Stanford University School of Medicine, Stanford, California
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Ellis, Matthew J.
- ORCID: https://orcid.org/0000-0002-8467-8534
- Other Affiliation: Lester and Sue Smith Breast Center, Baylor College of Medicine, Houston, Texas
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Bose, Ron
- Other Affiliation: Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri
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Ma, Cynthia X.
- Abstract
PURPOSE: HER2 mutations (HER2mut) induce endocrine resistance in estrogen receptor-positive (ER+) breast cancer. PATIENTS AND METHODS: In this single-arm multi-cohort phase II trial, we evaluated the efficacy of neratinib plus fulvestrant in patients with ER+/HER2mut, HER2 non-amplified metastatic breast cancer (MBC) in the fulvestrant-treated (n = 24) or fulvestrant-naïve cohort (n = 11). Patients with ER-negative (ER-)/HER2mut MBC received neratinib monotherapy in an exploratory ER- cohort (n = 5). RESULTS: The clinical benefit rate [CBR (95% confidence interval)] was 38% (18%-62%), 30% (7%-65%), and 25% (1%-81%) in the fulvestrant-treated, fulvestrant-naïve, and ER- cohorts, respectively. Adding trastuzumab at progression in 5 patients resulted in three partial responses and one stable disease ≥24 weeks. CBR appeared positively associated with lobular histology and negatively associated with HER2 L755 alterations. Acquired HER2mut were detected in 5 of 23 patients at progression. CONCLUSIONS: Neratinib and fulvestrant are active for ER+/HER2mut MBC. Our data support further evaluation of dual HER2 blockade for the treatment of HER2mut MBC.
- Date of publication
- January 18, 2022
- Keyword
- metastatic breast cancer
- efficacy
- negatively
- response
- lobular histology
- neratinib
- alterations
- endocrine resistance
- HER2-mutant
- combination
- histology
- trastuzumab
- evaluation
- fulvestrant
- receptor-positive
- data
- ER cohort
- resistance
- cancer
- estrogen receptor-positive
- mutations
- CBR
- breast cancer
- efficacy of neratinib
- associated with lobular histology
- benefit rate
- progression
- HER2 mutations
- cohort
- phase
- neratinib monotherapy
- rate
- blockade
- monotherapy
- breast
- weeks
- treatment
- estrogen
- clinical benefit rate
- patients
- partial response
- HER2 blockade
- HER2
- DOI
- Identifier
- Dimensions ID: pub.1144795550
- PMID: 35046057
- DOI: https://dx.doi.org/10.1158/1078-0432.ccr-21-3418
- Resource type
- Article
- Rights statement
- In Copyright
- Journal title
- Clinical Cancer Research
- Journal volume
- 28
- Journal issue
- 7
- Page start
- 1258
- Page end
- 1267
- Funder
- Congressionally Directed Medical Research Programs
- ISSN
- 1557-3265
- 1078-0432
- Publisher
- American Association for Cancer Research (AACR)
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- Parents:
- In Collection:
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