Literature DB >> 22646765

BRIM-1, -2 and -3 trials: improved survival with vemurafenib in metastatic melanoma patients with a BRAF(V600E) mutation.

Kate Young1, Anna Minchom, James Larkin.   

Abstract

Following Phase I and II studies revealing vemurafenib to be a safe potent inhibitor of mutated BRAF in patients with metastatic melanoma, a multicenter randomized Phase III trial was carried out to compare vemurafenib with dacarbazine in treatment-naive patients. The interim analysis results from this trial, BRIM-3, were sufficient for an independent data and safety monitoring board to recommend crossover from dacarbazine to vemurafenib, vemurafenib being associated with a relative risk reduction of 63% in the risk of death and 74% in the risk of death or disease progression compared with dacarbazine (p < 0.001 for both comparisons) with an acceptable toxicity profile. Such striking results have prompted analysis of our approach to the classification and treatment of metastatic melanoma in an age of molecular markers and targeted therapy.

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Year:  2012        PMID: 22646765     DOI: 10.2217/fon.12.43

Source DB:  PubMed          Journal:  Future Oncol        ISSN: 1479-6694            Impact factor:   3.404


  25 in total

Review 1.  Recent advances in the treatment of melanoma with BRAF and MEK inhibitors.

Authors:  Eva Muñoz-Couselo; Jesús Soberino García; José Manuel Pérez-García; Vanesa Ortega Cebrián; Javier Cortés Castán
Journal:  Ann Transl Med       Date:  2015-09

2.  The role of eIF4E in response and acquired resistance to vemurafenib in melanoma.

Authors:  Yao Zhan; Michael S Dahabieh; Arjuna Rajakumar; Monica C Dobocan; Marie-Noël M'Boutchou; Christophe Goncalves; Shiru L Lucy; Filippa Pettersson; Ivan Topisirovic; Léon van Kempen; Sonia V Del Rincón; Wilson H Miller
Journal:  J Invest Dermatol       Date:  2015-01-23       Impact factor: 8.551

3.  BRAF- and MEK-Targeted Small Molecule Inhibitors Exert Enhanced Antimelanoma Effects in Combination With Oncolytic Reovirus Through ER Stress.

Authors:  Victoria Roulstone; Malin Pedersen; Joan Kyula; David Mansfield; Aadil A Khan; Grainne McEntee; Michelle Wilkinson; Eleni Karapanagiotou; Matt Coffey; Richard Marais; Adel Jebar; Fiona Errington-Mais; Alan Melcher; Richard Vile; Hardev Pandha; Martin McLaughlin; Kevin J Harrington
Journal:  Mol Ther       Date:  2015-01-26       Impact factor: 11.454

4.  Genetic variants in Hippo pathway genes YAP1, TEAD1 and TEAD4 are associated with melanoma-specific survival.

Authors:  Hua Yuan; Hongliang Liu; Zhensheng Liu; Dakai Zhu; Christopher I Amos; Shenying Fang; Jeffrey E Lee; Qingyi Wei
Journal:  Int J Cancer       Date:  2015-01-28       Impact factor: 7.396

5.  Melanoma of the oral cavity: pathogenesis, dermoscopy, clinical features, staging and management.

Authors:  Olga Warszawik-Hendzel; Monika Słowińska; Małgorzata Olszewska; Lidia Rudnicka
Journal:  J Dermatol Case Rep       Date:  2014-09-30

6.  Evaluation of (68)Ga- and (177)Lu-DOTA-PEG4-LLP2A for VLA-4-Targeted PET Imaging and Treatment of Metastatic Melanoma.

Authors:  Wissam Beaino; Jessie R Nedrow; Carolyn J Anderson
Journal:  Mol Pharm       Date:  2015-05-08       Impact factor: 4.939

Review 7.  The prognostic value of BRAF mutation in colorectal cancer and melanoma: a systematic review and meta-analysis.

Authors:  Gholamreza Safaee Ardekani; Seyed Mehdi Jafarnejad; Larry Tan; Ardavan Saeedi; Gang Li
Journal:  PLoS One       Date:  2012-10-09       Impact factor: 3.240

8.  Genetic alteration of Chinese patients with rectal mucosal melanoma.

Authors:  Huan Li; Lujing Yang; Yumei Lai; Xintong Wang; Xinyin Han; Siyao Liu; Dongliang Wang; Xiaojuan Li; Nana Hu; Yan Kong; Lu Si; Zhongwu Li
Journal:  BMC Cancer       Date:  2021-05-27       Impact factor: 4.430

9.  Genetics of melanoma.

Authors:  Janet Wangari-Talbot; Suzie Chen
Journal:  Front Genet       Date:  2013-01-25       Impact factor: 4.599

Review 10.  Activated Ras as a Therapeutic Target: Constraints on Directly Targeting Ras Isoforms and Wild-Type versus Mutated Proteins.

Authors:  Raymond R Mattingly
Journal:  ISRN Oncol       Date:  2013-10-31
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