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本文引用的文献

1
RAF inhibitor resistance is mediated by dimerization of aberrantly spliced BRAF(V600E).RAF 抑制剂耐药性是由异常剪接的 BRAF(V600E)二聚化介导的。
Nature. 2011 Nov 23;480(7377):387-90. doi: 10.1038/nature10662.
2
BRAF mutations in advanced cancers: clinical characteristics and outcomes.晚期癌症中的 BRAF 突变:临床特征和结局。
PLoS One. 2011;6(10):e25806. doi: 10.1371/journal.pone.0025806. Epub 2011 Oct 19.
3
Regression does not predict nodal metastasis or survival in patients with cutaneous melanoma.回归分析无法预测皮肤黑色素瘤患者的淋巴结转移情况或生存率。
Am Surg. 2011 Aug;77(8):1009-13.
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Lymphovascular invasion as a prognostic factor in melanoma.淋巴管浸润作为黑色素瘤的一个预后因素。
Am Surg. 2011 Aug;77(8):992-7.
5
Improved survival with vemurafenib in melanoma with BRAF V600E mutation.BRAF V600E 突变型黑色素瘤患者采用威罗菲尼治疗后生存改善。
N Engl J Med. 2011 Jun 30;364(26):2507-16. doi: 10.1056/NEJMoa1103782. Epub 2011 Jun 5.
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Thin melanoma.薄型黑素瘤。
Arch Pathol Lab Med. 2011 Mar;135(3):342-6. doi: 10.5858/2009-0479-RA.1.
7
Targeted therapies in metastatic melanoma: toward a clinical breakthrough?转移性黑色素瘤的靶向治疗:临床突破在望?
Anticancer Agents Med Chem. 2010 Nov 1;10(9):661-5. doi: 10.2174/187152010794479834.
8
Targeting BRAF for patients with melanoma.针对黑色素瘤患者的 BRAF 靶向治疗。
Br J Cancer. 2011 Feb 1;104(3):392-8. doi: 10.1038/sj.bjc.6606030. Epub 2010 Dec 7.
9
Prognostication in thin cutaneous melanomas.薄型皮肤黑色素瘤的预后预测。
Arch Pathol Lab Med. 2010 Dec;134(12):1758-63. doi: 10.5858/2009-0653-RAR.1.
10
The Role of B-RAF Mutations in Melanoma and the Induction of EMT via Dysregulation of the NF-κB/Snail/RKIP/PTEN Circuit.B-RAF突变在黑色素瘤中的作用以及通过NF-κB/蜗牛蛋白/RKIP/PTEN信号通路失调诱导上皮-间质转化
Genes Cancer. 2010 May;1(5):409-420. doi: 10.1177/1947601910373795.

转移性薄黑素瘤患者对BRAF抑制剂有良好的临床和影像学反应。

Good clinical and radiological response to BRAF inhibitor in patient with metastatic thin melanoma.

作者信息

Quintyne Keith Ian, Baker Shirley, Wallis Fintan, Gupta Rajnish

机构信息

Medical Oncology Department, Mid-Western Regional Hospital, and Stokes Research Institute, University of Limerick, Limerick, Ireland.

出版信息

BMJ Case Rep. 2012 Jun 28;2012:bcr1120115202. doi: 10.1136/bcr.11.2011.5202.

DOI:10.1136/bcr.11.2011.5202
PMID:22744255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3448363/
Abstract

The authors herein report the case of a 32-year-old man with advancing metastatic malignant melanoma, who has progressed through all previous lines of therapy, presenting with ongoing respiratory tract symptoms of exertional shortness of breath and cough. CT restaging confirmed clinical findings of deteriorating pulmonary disease; histological review revealed V600E BRAF mutation. He was started on targeted biological therapy with BRAF inhibitor GSK2118436, and is having a good clinical and radiological response without significant lasting toxicity.

摘要

本文作者报告了一例32岁进展期转移性恶性黑色素瘤男性患者的病例,该患者此前所有治疗方案均已无效,目前存在劳力性呼吸急促和咳嗽等持续呼吸道症状。CT重新分期证实了肺部疾病恶化的临床发现;组织学检查显示存在V600E BRAF突变。他开始接受BRAF抑制剂GSK2118436的靶向生物治疗,目前临床和影像学反应良好,且无明显的持续性毒性。