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

被引:23
作者
Seo, Takuji [1 ]
Noguchi, Emi [1 ]
Yoshida, Masayuki [2 ]
Mori, Taisuke [2 ]
Tanioka, Maki [1 ]
Sudo, Kazuki [1 ]
Shimomura, Akihiko [1 ]
Yonemori, Kan [1 ]
Fujiwara, Yasuhiro [1 ]
Tamura, Kenji [1 ]
机构
[1] Natl Canc Ctr, Dept Breast & Med Oncol, Chuo Ku, 5-1-1 Tsukiji, Tokyo 1040045, Japan
[2] Natl Canc Ctr, Dept Pathol & Clin Labs, Chuo Ku, 5-1-1 Tsukiji, Tokyo 1040045, Japan
关键词
SOLID TUMORS; CANCER; MELANOMA; AMPLIFICATION; INHIBITION; SURVIVAL; GENE; EGFR;
D O I
10.1155/2020/2518383
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. Case Presentation. 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.
引用
收藏
页数:6
相关论文
共 25 条
[11]   The differences in the histological types of breast cancer and the response to neoadjuvant chemotherapy: The relationship between the outcome and the clinicopathological characteristics [J].
Nagao, Tomoya ;
Kinoshita, Takayuki ;
Hojo, Takashi ;
Tsuda, Hitoshi ;
Tamura, Kenji ;
Fujiwara, Yasuhiro .
BREAST, 2012, 21 (03) :289-295
[12]   Survival Outcomes of Metaplastic Breast Cancer Patients: Results from a US Population-based Analysis [J].
Nelson, Rebecca A. ;
Guye, Mary L. ;
Luu, Thehang ;
Lai, Lily L. .
ANNALS OF SURGICAL ONCOLOGY, 2015, 22 (01) :24-31
[13]   Metaplastic carcinoma of the breast [J].
Okada, Nao ;
Hasebe, Takahiro ;
Iwasaki, Motoki ;
Tamura, Nobuko ;
Akashi-Tanaka, Sadako ;
Hojo, Takashi ;
Shibata, Tatsuhiro ;
Sasajima, Yuko ;
Kanai, Yae ;
Kinoshita, Takayuki .
HUMAN PATHOLOGY, 2010, 41 (07) :960-970
[14]   Characteristics and treatment of metaplastic breast cancer: Analysis of 892 cases from the National Cancer Data Base [J].
Pezzi, Christopher M. ;
Patel-Parekh, Lina ;
Cole, Karin ;
Franko, Jan ;
Klimberg, V. Suzanne ;
Bland, Kirby .
ANNALS OF SURGICAL ONCOLOGY, 2007, 14 (01) :166-173
[15]   Phenotypic and molecular characterization of the claudin-low intrinsic subtype of breast cancer [J].
Prat, Aleix ;
Parker, Joel S. ;
Karginova, Olga ;
Fan, Cheng ;
Livasy, Chad ;
Herschkowitz, Jason I. ;
He, Xiaping ;
Perou, Charles M. .
BREAST CANCER RESEARCH, 2010, 12 (05)
[16]   Prognostic factors in metaplastic carcinoma of the breast: a multi-institutional study [J].
Rakha, E. A. ;
Tan, P. H. ;
Varga, Z. ;
Tse, G. M. ;
Shaaban, A. M. ;
Climent, F. ;
van Deurzen, C. H. M. ;
Purnell, D. ;
Dodwell, D. ;
Chan, T. ;
Ellis, I. O. .
BRITISH JOURNAL OF CANCER, 2015, 112 (02) :283-289
[17]   EGFR amplification and lack of activating mutations in metaplastic breast carcinomas [J].
Reis, J. S. ;
Pinheiro, C. ;
Lambros, M. B. K. ;
Milanezi, F. ;
Carvalho, S. ;
Savage, K. ;
Simpson, P. T. ;
Jones, C. ;
Swift, S. ;
Mackay, A. ;
Reis, R. M. ;
Hornick, J. L. ;
Pereira, E. M. ;
Baltazar, F. ;
Fletcher, C. D. M. ;
Ashworth, A. ;
Lakhani, S. R. ;
Schmitt, F. C. .
JOURNAL OF PATHOLOGY, 2006, 209 (04) :445-453
[18]   Metaplastic breast carcinomas exhibit EGFR, but not HER2, gene amplification and overexpression:: immunohistochemical and chromogenic in situ hybridization analysis [J].
Reis, JS ;
Milanezi, F ;
Carvalho, S ;
Simpson, PT ;
Steele, D ;
Savage, K ;
Lambros, MBK ;
Pereira, EM ;
Nesland, JM ;
Lakhani, SR ;
Schmitt, FC .
BREAST CANCER RESEARCH, 2005, 7 (06) :R1028-R1035
[19]   Improved Overall Survival in Melanoma with Combined Dabrafenib and Trametinib [J].
Robert, Caroline ;
Karaszewska, Boguslawa ;
Schachter, Jacob ;
Rutkowski, Piotr ;
Mackiewicz, Andrzej ;
Stroiakovski, Daniil ;
Lichinitser, Michael ;
Dummer, Reinhard ;
Grange, Florent ;
Mortier, Laurent ;
Chiarion-Sileni, Vanna ;
Drucis, Kamil ;
Krajsova, Ivana ;
Hauschild, Axel ;
Lorigan, Paul ;
Wolter, Pascal ;
Long, Georgina V. ;
Flaherty, Keith ;
Nathan, Paul ;
Ribas, Antoni ;
Martin, Anne-Marie ;
Sun, Peng ;
Crist, Wendy ;
Legos, Jeff ;
Rubin, Stephen D. ;
Little, Shonda M. ;
Schadendorf, Dirk .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (01) :30-39
[20]   Genomic Profiling of Advanced-Stage, Metaplastic Breast Carcinoma by Next-Generation Sequencing Reveals Frequent, Targetable Genomic Abnormalities and Potential New Treatment Options [J].
Ross, Jeffrey S. ;
Badve, Sunil ;
Wang, Kai ;
Sheehan, Christine E. ;
Boguniewicz, Ann B. ;
Otto, Geoff A. ;
Yelensky, Roman ;
Lipson, Doron ;
Ali, Siraj ;
Morosini, Deborah ;
Chliemlecki, Juliann ;
Elvin, Julia A. ;
Miller, Vincent A. ;
Stephens, Philip J. .
ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 2015, 139 (05) :642-649