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SDHB 相关性恶性嗜铬细胞瘤对替莫唑胺-卡培他滨有显著反应。

A SDHB malignant paraganglioma with dramatic response to temozolomide-capecitabine.

机构信息

Hospices Civils de Lyon, Hôpital Edouard Herriot, Fédération des Spécialités Digestives, Place d'Arsonval, Lyon cedex 03, France.

出版信息

Eur J Endocrinol. 2012 Jun;166(6):1107-11. doi: 10.1530/EJE-11-1098. Epub 2012 Mar 19.

Abstract

Ten percent of paragangliomas are malignant and one-third occurs in a genetic background. We report a case of succinate dehydrogenase subunit B (SDHB)-related malignant paraganglioma with dramatic response to temozolomide and capecitabine regimen (decrease in tumor size of 70% with RECIST criteria). Tumor cells harbored a new mutation in SDHB gene and showed aberrant hypermethylation of O6-methylguanine-DNA-methyltransferase promoter. Our report suggests the importance of molecular predictive factors of response for the selection of chemotherapeutic as well as targeted agents. This observation points to a possible genotype response to treatment relationships, which could help to design tailor-made treatments in the future.

摘要

10%的副神经节瘤为恶性肿瘤,三分之一发生于遗传背景中。我们报告了一例琥珀酸脱氢酶亚基 B(SDHB)相关的恶性副神经节瘤,该肿瘤对替莫唑胺和卡培他滨方案(RECIST 标准下肿瘤大小缩小 70%)有显著反应。肿瘤细胞携带 SDHB 基因的新突变,并表现出 O6-甲基鸟嘌呤-DNA-甲基转移酶启动子的异常高甲基化。我们的报告表明了对化疗和靶向药物选择的分子预测因素的重要性。这一观察结果表明了可能存在的基因型与治疗反应的关系,这有助于未来设计定制化的治疗方案。

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