Literature DB >> 28002643

Clinical and therapeutic implications of BRAF mutation heterogeneity in metastatic melanoma.

Nima Mesbah Ardakani1,2, Connull Leslie1,2, Fabienne Grieu-Iacopetta1, Wei-Sen Lam3, Charley Budgeon4, Michael Millward3,5, Benhur Amanuel1,2.   

Abstract

Heterogeneity of BRAF mutation in melanoma has been a controversial subject. Quantitative data on BRAF allele frequency (AF) are sparse, and the potential relationship with response to BRAF inhibitors (BRAFi) in patients with metastatic melanoma is unknown. We quantitatively measured BRAF AF in a cohort of treatment naïve metastatic melanoma samples by pyrosequencing and correlated with survival data in patients treated with BRAFi as part of their clinical care. Fifty-two samples from 50 patients were analysed. BRAF V600E mutations were detected in 71.1% of samples followed by V600K (25%) and V600R (3.9%). There was a wide range of AF from 3.9% to 80.3% (median 41.3%). In 33 patients treated with BRAFi, there was no difference in overall or progression-free survival when the patients were categorized into high or low AF groups. There was no correlation between AF and degree of response, and no difference in survival based on genotype.
© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  BRAF inhibitor; BRAF mutation; allele frequency; heterogeneity; malignant melanoma; pyrosequencing

Mesh:

Substances:

Year:  2017        PMID: 28002643     DOI: 10.1111/pcmr.12569

Source DB:  PubMed          Journal:  Pigment Cell Melanoma Res        ISSN: 1755-1471            Impact factor:   4.693


  6 in total

1.  Microradiopharmaceutical for Metastatic Melanoma.

Authors:  Thiago Goulart Rosa; Sofia Nascimento Dos Santos; Terezina de Jesus Andreoli Pinto; Daniele Dal Molim Ghisleni; Thereza Christina Barja-Fidalgo; Eduardo Ricci-Junior; Mohammed Al-Qahtani; Jan Kozempel; Emerson Soares Bernardes; Ralph Santos-Oliveira
Journal:  Pharm Res       Date:  2017-10-23       Impact factor: 4.200

Review 2.  BRAF Heterogeneity in Melanoma.

Authors:  Takamichi Ito; Yuka Tanaka; Maho Murata; Yumiko Kaku-Ito; Kazuhisa Furue; Masutaka Furue
Journal:  Curr Treat Options Oncol       Date:  2021-02-08

3.  Dynamic and unpredictable changes in mutant allele fractions of BRAF and NRAS during visceral progression of cutaneous malignant melanoma.

Authors:  V Doma; S Kárpáti; E Rásó; T Barbai; J Tímár
Journal:  BMC Cancer       Date:  2019-08-07       Impact factor: 4.430

4.  Immunohistochemical and Molecular Features of Melanomas Exhibiting Intratumor and Intertumor Histomorphologic Heterogeneity.

Authors:  Haider A Mejbel; Sri Krishna C Arudra; Dinesh Pradhan; Carlos A Torres-Cabala; Priyadharsini Nagarajan; Michael T Tetzlaff; Jonathan L Curry; Doina Ivan; Dzifa Y Duose; Raja Luthra; Victor G Prieto; Leomar Y Ballester; Phyu P Aung
Journal:  Cancers (Basel)       Date:  2019-11-02       Impact factor: 6.639

5.  Cylindromatosis Is Required for Survival of a Subset of Melanoma Cells.

Authors:  Ting La; Lei Jin; Xiao Ying Liu; Ze Hua Song; Margaret Farrelly; Yu Chen Feng; Xu Guang Yan; Yuan Yuan Zhang; Rick F Thorne; Xu Dong Zhang; Liu Teng
Journal:  Oncol Res       Date:  2020-04-06       Impact factor: 5.574

Review 6.  Intratumor and Intertumor Heterogeneity in Melanoma.

Authors:  Tomasz M Grzywa; Wiktor Paskal; Paweł K Włodarski
Journal:  Transl Oncol       Date:  2017-10-24       Impact factor: 4.243

  6 in total

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