Carcinoma ex pleomorphic adenoma: case report and options for systemic therapy

被引:12
作者
Chooback, N. [1 ]
Shen, Y. [2 ]
Jones, M. [2 ]
Kasaian, K. [2 ]
Martin, M. [3 ]
Ng, T. [4 ]
Thomson, T. [5 ]
Marra, M. [2 ]
Laskin, J. [1 ]
Ho, C. [1 ]
机构
[1] BC Canc Agcy, Dept Med Oncol, Vancouver, BC, Canada
[2] BC Canc Res Ctr, Vancouver, BC, Canada
[3] BC Canc Agcy, Dept Diagnost Imaging, Vancouver, BC, Canada
[4] Vancouver Coastal Hlth Res Inst, Dept Pathol & Lab Med, Vancouver, BC, Canada
[5] BC Canc Agcy, Dept Pathol & Lab Med, Vancouver, BC, Canada
关键词
Carcinoma ex pleomorphic adenoma; chemotherapy; cyclophosphamide; doxorubicin; cisplatin; SALIVARY DUCT CARCINOMA; MALIGNANT-TRANSFORMATION; GLAND; EXPRESSION; CHEMOTHERAPY; PLAG1; CYCLOPHOSPHAMIDE; DOXORUBICIN; CISPLATIN; PATIENT;
D O I
10.3747/co.24.3588
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The most common benign salivary tumour is a pleomorphic adenoma. Transformation to malignancy, carcinoma ex pleomorphic adenoma (CXPA), occurs in 6% of cases. Management focuses on surgical resection and radiotherapy; however, rare cases require systemic management. We present the case of a 60-year-old woman with a CXPA of the left parotid gland who required systemic therapy for locally recurrent disease. Treatment options were guided by the literature concerning malignant salivary gland tumour and by whole-genome and transcriptome sequencing of the tumour. The patient received multiple systemic agents during the course of her disease, with cyclophosphamide-doxorubicin-cisplatin providing the best control (partial response). Genome-and transcriptome-directed therapy, including sorafenib and vismodegib, were utilized with limited clinical benefit. Malignant transformation in CXPA is a complex process, and therapy directed at a single tumour pathway might not be sufficient to control disease.
引用
收藏
页码:E251 / E254
页数:4
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