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PTCH1 突变与转移性透明细胞样去分化癌患者相关。

PTCH1 Mutation in a Patient With Metastatic Undifferentiated Carcinoma With Clear Cell Change.

机构信息

Melanoma and Skin Cancer Program, UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, California.

Oschsner Clinical School, University of Queensland, New Orleans, Louisiana; and.

出版信息

J Natl Compr Canc Netw. 2019 Jul 1;17(7):778-783. doi: 10.6004/jnccn.2019.7313.

Abstract

Clear cell basal cell carcinoma (BCC) is an unusual variant of BCC. Its pathogenesis, prognosis, and optimal management remain poorly described due to its rarity. This report presents a 51-year-old man with a history of excised BCC and cutaneous squamous cell carcinomas of the face, with multiple recurrent poorly differentiated carcinomas with clear cell changes of the shoulder for which further classification using conventional histologic means was not possible. His tumor tissue was sent to Foundation Medicine for testing, which revealed a high number of pathogenic genomic alterations, including a mutation in PTCH1. He was diagnosed with dedifferentiated BCC and started on vismodegib. He developed lung metastases while receiving vismodegib, and his disease continued to progress while he was undergoing treatment in a phase I clinical trial. Given the high number of pathogenic alterations suggestive of high tumor mutational burden, immunotherapy was considered and off-label authorization was obtained for treatment with a PD-1 antibody (pembrolizumab). He had a dramatic disease response after 4 infusions of pembrolizumab. Molecular testing was instrumental in determining the correct diagnosis and formulating appropriate treatment options for this patient. Molecular profiling of metastatic BCCs and its subtypes is essential to the development of effective targeted therapies and combination approaches.

摘要

透明细胞基底细胞癌(BCC)是一种不常见的 BCC 变体。由于其罕见性,其发病机制、预后和最佳治疗方法仍描述不佳。本报告介绍了一名 51 岁男性,他曾患有切除的 BCC 和面部皮肤鳞状细胞癌,肩部有多个复发性低分化癌,伴有透明细胞改变,常规组织学方法无法进一步分类。他的肿瘤组织被送到 Foundation Medicine 进行检测,结果显示存在大量致病性基因组改变,包括 PTCH1 突变。他被诊断为去分化 BCC,并开始使用维莫德吉治疗。他在接受维莫德吉治疗时发生了肺转移,并且在接受 I 期临床试验治疗时疾病继续进展。鉴于大量致病性改变提示肿瘤突变负担高,考虑进行免疫治疗,并获得了 PD-1 抗体(pembrolizumab)的非适应证治疗批准。在接受 pembrolizumab 治疗 4 次后,他的疾病有了显著缓解。分子检测对确定该患者的正确诊断和制定适当的治疗方案至关重要。对转移性 BCC 及其亚型进行分子谱分析对于开发有效的靶向治疗和联合治疗方法至关重要。

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