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Journal ArticleDOI

Dabrafenib and trametinib versus dabrafenib and placebo for Val600 BRAF-mutant melanoma: a multicentre, double-blind, phase 3 randomised controlled trial

TLDR
The improvement in overall survival establishes the combination of dabrafenib and trametinib as the standard targeted treatment for BRAF Val600 mutation-positive melanoma.
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This article is published in The Lancet.The article was published on 2015-08-01. It has received 1099 citations till now. The article focuses on the topics: Dabrafenib & Trametinib.

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Pediatric Glioma: An Update of Diagnosis, Biology, and Treatment.

TL;DR: In this paper, the authors summarize recent knowledge to provide an overview of pediatric gliomas, which are major pediatric CNS tumors, and describe recent developments in strategies employed for their diagnosis and treatment.
Journal ArticleDOI

Dabrafenib plus trametinib in patients with relapsed/refractory BRAF V600E mutation–positive hairy cell leukemia

TL;DR: Dabrafenib plus trametinib demonstrated durable responses with a manageable safety profile consistent with previous observations in other indications and should be considered as a rituximab-free therapeutic option for patients with relapsed/refractory BRAF V600E mutation-positive HCL.
Journal ArticleDOI

Immunometabolic Network Interactions of the Kynurenine Pathway in Cutaneous Malignant Melanoma.

TL;DR: In this paper, the authors show that mitogen-activated protein kinase pathway (MAPKIs) treatments are associated with alteration of 3-hydroxykynurenine and 3HAA concentrations and led to higher "CXCL11," and "KLRD1" expression that are involved in T and NK cells activation.
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Chemokine receptor 4 expression is correlated with the occurrence and prognosis of gastric cancer.

TL;DR: It is suggested that CXCR4 may affect the progression and prognosis of GC by influencing immune infiltration, TMB, CYT, tumor purity, and drug sensitivity.
References
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Journal ArticleDOI

A multiple testing procedure for clinical trials.

TL;DR: The overall size of the procedure is shown to be controlled with virtually the same accuracy as the single sample chi-square test based on N(m1 + m2) observations and the power is found to bevirtually the same.
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