Detailed imaging and genetic analysis reveal a secondary BRAF(L505H) resistance mutation and extensive intrapatient heterogeneity in metastatic BRAF mutant melanoma patients treated with vemurafenib

Publication date

2015-05

Authors

Hoogstraat, Marlous
Gadellaa-van Hooijdonk, Christa G.
Ubink, I.
Besselink, Nicolle J. M.
Pieterse, Mark
Veldhuis, WBORCID 0000-0002-9798-6843ISNI 0000000395578034
van Stralen, MORCID 0000-0002-3051-5000ISNI 0000000395962765
Meijer, Eelco F. J.
Willems, S. M.ISNI 0000000387897385
Hadders, Michael A.ISNI 0000000389558221

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Document Type

Article

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taverne

Abstract

Resistance to treatment is the main problem of targeted treatment for cancer. We followed ten patients during treatment with vemurafenib, by three-dimensional imaging. In all patients, only a subset of lesions progressed. Next-generation DNA sequencing was performed on sequential biopsies in four patients to uncover mechanisms of resistance. In two patients, we identified mutations that explained resistance to vemurafenib; one of these patients had a secondary BRAF L505H mutation. This is the first observation of a secondary BRAF mutation in a vemurafenib-resistant patient-derived melanoma sample, which confirms the potential importance of the BRAF L505H mutation in the development of therapy resistance. Moreover, this study hints toward an important role for tumor heterogeneity in determining the outcome of targeted treatments.

Keywords

BRAF, vemurafenib, intratumoral heterogeneity, therapy resistance, volumetric imaging analysis, GASTROINTESTINAL STROMAL TUMOR, ACQUIRED-RESISTANCE, RAF INHIBITION, CLONAL EVOLUTION, KINASE DOMAIN, MECHANISMS, IDENTIFICATION, IMATINIB, CANCER, DISPARITY, Taverne, Journal Article, Research Support, Non-U.S. Gov't

Citation

Hoogstraat, M, Gadellaa-van Hooijdonk, C G, Ubink, I, Besselink, N J M, Pieterse, M, Veldhuis, W, van Stralen, M, Meijer, E F J, Willems, S M, Hadders, M A, Kuilman, T, Krijgsman, O, Peeper, D S, Koudijs, M J, Cuppen, E, Voest, E E & Lolkema, M P 2015, 'Detailed imaging and genetic analysis reveal a secondary BRAF(L505H) resistance mutation and extensive intrapatient heterogeneity in metastatic BRAF mutant melanoma patients treated with vemurafenib', Pigment Cell and Melanoma Research, vol. 28, no. 3, pp. 318-323. https://doi.org/10.1111/pcmr.12347