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治疗中断后联合BRAF/MEK抑制控制颅内黑色素瘤转移的快速进展:一项临床挑战。

Rapid progression of intracranial melanoma metastases controlled with combined BRAF/MEK inhibition after discontinuation of therapy: a clinical challenge.

作者信息

Cagney Daniel N, Alexander Brian M, Hodi F Stephen, Buchbinder Elizabeth I, Ott Patrick A, Aizer Ayal A

机构信息

Department of Radiation Oncology, Brigham and Women's Hospital, Harvard Medical School, 75 Francis Street, Boston, MA, 02115, USA.

Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

出版信息

J Neurooncol. 2016 Sep;129(3):389-393. doi: 10.1007/s11060-016-2196-8. Epub 2016 Jul 11.

Abstract

Novel systemic therapies with anti-tumor activity in the brain including small molecules targeting BRAF and MEK, and immune checkpoint inhibition, offer the possibility of improved control of intracranial disease. A number of prospective trials support the judicious use of modern systemic therapies in patients with melanoma and limited brain metastases .The intracranial clinical course of patients who progress extracranially on BRAF/MEK inhibition remains poorly described in the literature. In this report, we highlight a series of clinical cases, with rapid progression of intracranial disease following discontinuation of dabrafenib/trametinib for extracranial disease progression or toxicity, a previously unreported finding in the medical literature with significant implications for patient care.

摘要

具有脑内抗肿瘤活性的新型全身治疗方法,包括靶向BRAF和MEK的小分子药物以及免疫检查点抑制,为改善颅内疾病的控制提供了可能性。多项前瞻性试验支持在黑色素瘤和脑转移灶有限的患者中合理使用现代全身治疗方法。BRAF/MEK抑制治疗后颅外病情进展的患者的颅内临床病程在文献中仍描述甚少。在本报告中,我们重点介绍了一系列临床病例,这些病例在因颅外疾病进展或毒性而停用达拉非尼/曲美替尼后,颅内疾病迅速进展,这是医学文献中此前未报道的发现,对患者护理具有重要意义。

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