A long-term surviving patient with recurrent low-grade serous ovarian carcinoma treated with the MEK1/2 inhibitor, selumetinib.

Gynecologic oncology research and practice Pub Date : 2016-05-05 eCollection Date: 2016-01-01 DOI:10.1186/s40661-016-0026-5
Munetaka Takekuma, Kwong K Wong, Robert L Coleman
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引用次数: 16

Abstract

Background: Selumetinib is a potent, selective, orally available, and non-ATP competitive small molecule inhibitor of mitogen-activated protein kinase kinase 1/2 (MEK1/2) that has demonstrated single agent activity in a number of solid tumor including recurrent low-grade serous ovarian carcinoma (LGSOC). However, the long-term prognosis of patients who receive selumetinib, as well as the late toxicity of the agent, have not yet been described.

Case presentation: In this case report, we present a patient with recurrent LGSOC with KRAS mutation whose tumor has not progressed and who has maintained a good general condition without severe toxicities following treatment with selumetinib for more than 7 years. Next generation sequencing of her tumor revealed a G12V mutation in KRAS. MAPK signaling inhibition plays a role in the biology of LGSOC.

Conclusions: Although biomarkers have yet to definitively define patients with LGSOC who are likely to respond to therapy, exploration of specific alterations should be pursued in an excersie to develop a reliable companion diagnostic test.

Abstract Image

Abstract Image

长期存活的复发性低级别浆液性卵巢癌患者接受MEK1/2抑制剂selumetinib治疗。
背景:Selumetinib是一种有效的,选择性的,口服的,非atp竞争性的丝裂原活化蛋白激酶1/2 (MEK1/2)的小分子抑制剂,已被证明在许多实体肿瘤中具有单药活性,包括复发性低级别浆液性卵巢癌(LGSOC)。然而,接受selumetinib治疗的患者的长期预后,以及该药物的晚期毒性,尚未被描述。病例介绍:在本病例报告中,我们报告了一位复发性LGSOC合并KRAS突变的患者,其肿瘤未进展,并且在接受selumetinib治疗超过7年后,总体状况良好,无严重毒性。她的肿瘤的下一代测序显示KRAS的G12V突变。MAPK信号抑制在LGSOC的生物学中起作用。结论:尽管生物标志物尚未明确定义可能对治疗有反应的LGSOC患者,但应该在一项试验中探索特定的改变,以开发可靠的伴随诊断测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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