Literature DB >> 29076950

Vemurafenib treatment for patients with locally advanced, unresectable stage IIIC or metastatic melanoma and activating exon 15 BRAF mutations other than V600E.

Sigrun Hallmeyer1, Rene Gonzalez, David H Lawson, Lee D Cranmer, Gerald P Linette, Igor Puzanov, Bret Taback, C Lance Cowey, Antoni Ribas, Gregory A Daniels, Timothy Moore, Geoffrey T Gibney, Hussein Tawbi, Eric Whitman, Geraldine Lee, Yong Mun, Shiyao Liu, Omid Hamid.   

Abstract

BRAF mutations are found in ~50% of metastatic melanomas, most commonly in codon V600. Vemurafenib improves progression-free survival and overall survival in patients with advanced BRAF-mutated melanoma. The results of a descriptive study evaluating vemurafenib in patients with advanced melanoma harbouring BRAF mutations other than V600E are reported. Eligible patients with stage IIIC or IV melanoma and non-V600E BRAF mutations received vemurafenib (960 mg, twice daily). End points included investigator-assessed best overall response rate (primary), time to response, duration of response, progression-free survival, overall survival and safety. Planned (V600K vs. non-V600K mutations) subgroup analyses were carried out. Thirty-one patients were enrolled; 13 (42%) had V600K mutations and 18 (58%) had other mutations. Investigator-assessed confirmed that the best overall response rate was 23% (95% confidence interval=10-41%) in the overall population, and was similar between patients with V600K mutations (23%; 95% confidence interval=5-54%) versus other mutations (22%; 95% confidence interval=6-48%). Responses were observed in patients with V600K (n=3), V600E2 (n=1), V600R (n=1), L597S (n=1) and D594G (n=1) mutations. No new safety signals were reported. Vemurafenib showed activity in patients with advanced melanoma with rarer BRAF mutations.

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Year:  2017        PMID: 29076950     DOI: 10.1097/CMR.0000000000000398

Source DB:  PubMed          Journal:  Melanoma Res        ISSN: 0960-8931            Impact factor:   3.599


  5 in total

Review 1.  Classifying BRAF alterations in cancer: new rational therapeutic strategies for actionable mutations.

Authors:  Matthew Dankner; April A N Rose; Shivshankari Rajkumar; Peter M Siegel; Ian R Watson
Journal:  Oncogene       Date:  2018-03-15       Impact factor: 9.867

2.  Lack of Response to Vemurafenib in Melanoma Carrying BRAF K601E Mutation.

Authors:  Fedor V Moiseyenko; Vitaliy V Egorenkov; Mikhail M Kramchaninov; Elizaveta V Artemieva; Svetlana N Aleksakhina; Maxim M Holmatov; Vladimir M Moiseyenko; Evgeny N Imyanitov
Journal:  Case Rep Oncol       Date:  2019-05-16

3.  RAC1 Alterations Induce Acquired Dabrafenib Resistance in Association with Anaplastic Transformation in a Papillary Thyroid Cancer Patient.

Authors:  Rozita Bagheri-Yarmand; Naifa L Busaidy; Elena McBeath; Brian P Danysh; Kurt W Evans; Tyler J Moss; Argun Akcakanat; Patrick K S Ng; Christina M Knippler; Jalyn A Golden; Michelle D Williams; Asha S Multani; Maria E Cabanillas; Kenna R Shaw; Funda Meric-Bernstam; Manisha H Shah; Matthew D Ringel; Marie Claude Hofmann
Journal:  Cancers (Basel)       Date:  2021-09-30       Impact factor: 6.575

4.  Detection of BRAF, NRAS, KIT, GNAQ, GNA11 and MAP2K1/2 mutations in Russian melanoma patients using LNA PCR clamp and biochip analysis.

Authors:  Marina Emelyanova; Lilit Ghukasyan; Ivan Abramov; Oxana Ryabaya; Evgenia Stepanova; Anna Kudryavtseva; Asiya Sadritdinova; Cholpon Dzhumakova; Tatiana Belysheva; Sergey Surzhikov; Lyudmila Lyubchenko; Alexander Zasedatelev; Tatiana Nasedkina
Journal:  Oncotarget       Date:  2017-04-10

5.  Prevalence of class I-III BRAF mutations among 114,662 cancer patients in a large genomic database.

Authors:  Jeff Owsley; Matthew K Stein; Jason Porter; Gino K In; Mohamed Salem; Steven O'Day; Andrew Elliott; Kelsey Poorman; Geoffrey Gibney; Ari VanderWalde
Journal:  Exp Biol Med (Maywood)       Date:  2020-10-05
  5 in total

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