» Articles » PMID: 32206360

Response to Dabrafenib and Trametinib of a Patient with Metaplastic Breast Carcinoma Harboring a BRAF V600E Mutation

Overview
Publisher Wiley
Specialty Oncology
Date 2020 Mar 25
PMID 32206360
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Metaplastic breast carcinomas are rare and carry poor prognoses. They are also more aggressive than other breast cancers and are known for their resistance to chemotherapy. Prolonged treatment with dabrafenib and trametinib is a therapy for malignant melanoma that improves the progression-free survival and overall survival. Such molecular-targeted therapies are also being developed for cancers with BRAF mutation, a driver of malignant melanoma. . A 57-year-old woman with metaplastic breast cancer and chemotherapy-refractory massive pleural effusion. After contained anthracycline regimen failure, her breast cancer progressed to an advanced stage. We ordered next-generation sequencing- (NGS-) based tumor molecular profiling from core needle biopsy of the breast. The NGS report indicated the presence of a BRAF V600E mutation. After initiation of dabrafenib and trametinib, her symptom and the pleural effusion were decreased. The first assessment of CT scans showed a decreased pleural effusion and shrunken subcutaneous lesions. Approximately 2 weeks later, a new lesion appeared. She died from 12 weeks after initiation of dabrafenib and trametinib treatment.

Conclusion: To the best of our knowledge, this is the first report of BRAF mutation breast cancer treated with dabrafenib and trametinib and it heralds the possibility of targeted therapy for rare breast cancers.

Citing Articles

Potential Drug Synergy Through the ERBB2 Pathway in HER2+ Breast Tumors.

Rojas-Salazar Y, Gomez-Montanez E, Rojas-Salazar J, Anda-Jauregui G, Hernandez-Lemus E Int J Mol Sci. 2024; 25(23).

PMID: 39684551 PMC: 11641395. DOI: 10.3390/ijms252312840.


Dissection of triple-negative breast cancer microenvironment and identification of potential therapeutic drugs using single-cell RNA sequencing analysis.

Cheng W, Mi W, Wang S, Wang X, Jiang H, Chen J J Pharm Anal. 2024; 14(8):100975.

PMID: 39263352 PMC: 11388705. DOI: 10.1016/j.jpha.2024.100975.


DeepDRA: Drug repurposing using multi-omics data integration with autoencoders.

Mohammadzadeh-Vardin T, Ghareyazi A, Gharizadeh A, Abbasi K, Rabiee H PLoS One. 2024; 19(7):e0307649.

PMID: 39058696 PMC: 11280260. DOI: 10.1371/journal.pone.0307649.


Translational Aspects in Metaplastic Breast Carcinoma.

Barrientos-Toro E, Ding Q, Raso M Cancers (Basel). 2024; 16(7).

PMID: 38611109 PMC: 11011105. DOI: 10.3390/cancers16071433.


Lung Fibroblasts Take up Breast Cancer Cell-derived Extracellular Vesicles Partially Through MEK2-dependent Macropinocytosis.

Wan Y, Zhao Y, Cao M, Wang J, Tran S, Song Z Cancer Res Commun. 2024; 4(1):170-181.

PMID: 38259097 PMC: 10802141. DOI: 10.1158/2767-9764.CRC-23-0316.


References
1.
Reis-Filho J, Milanezi F, Carvalho S, Simpson P, Steele D, Savage K . Metaplastic breast carcinomas exhibit EGFR, but not HER2, gene amplification and overexpression: immunohistochemical and chromogenic in situ hybridization analysis. Breast Cancer Res. 2005; 7(6):R1028-35. PMC: 1410747. DOI: 10.1186/bcr1341. View

2.
Solit D, Rosen N . Resistance to BRAF inhibition in melanomas. N Engl J Med. 2011; 364(8):772-4. DOI: 10.1056/NEJMcibr1013704. View

3.
Reis-Filho J, Pinheiro C, Lambros M, Milanezi F, Carvalho S, Savage K . EGFR amplification and lack of activating mutations in metaplastic breast carcinomas. J Pathol. 2006; 209(4):445-53. DOI: 10.1002/path.2004. View

4.
Pezzi C, Patel-Parekh L, Cole K, Franko J, Klimberg V, Bland K . Characteristics and treatment of metaplastic breast cancer: analysis of 892 cases from the National Cancer Data Base. Ann Surg Oncol. 2006; 14(1):166-73. DOI: 10.1245/s10434-006-9124-7. View

5.
Okada N, Hasebe T, Iwasaki M, Tamura N, Akashi-Tanaka S, Hojo T . Metaplastic carcinoma of the breast. Hum Pathol. 2010; 41(7):960-70. DOI: 10.1016/j.humpath.2009.11.013. View