Literature DB >> 33455008

Melanoma brain metastases: Biological basis and novel therapeutic strategies.

Manali Phadke1, Alpaslan Ozgun2, Zeynep Eroglu2, Keiran S M Smalley1,2.   

Abstract

The development of brain metastases is the deadliest complication of advanced melanoma and has long been associated with a dismal prognosis. The recent years have seen incredible progress in the development of therapies for melanoma brain metastases (MBM), with both targeted therapies (the BRAF-MEK inhibitor combination) and immune checkpoint inhibitors (the anti-CTLA-4, anti-PD-1 combination) showing impressive levels of activity. Despite this, durations of response for these therapies remain lower at intracranial sites of metastasis compared to extracranial metastases and it has been suggested that there are unique features of the brain microenvironment that contribute to therapeutic escape. In this review, we outline the latest research into the biology and pathophysiology of melanoma brain metastasis development and progression. We then discuss the current status of clinical trial that are open to patients with MBM and end by describing the ongoing challenges for the field.
© 2021 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

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Keywords:  CNS; brain metastases; immunology; melanoma; metabolism

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Year:  2021        PMID: 33455008     DOI: 10.1111/exd.14286

Source DB:  PubMed          Journal:  Exp Dermatol        ISSN: 0906-6705            Impact factor:   3.960


  1 in total

1.  HSP70 inhibition blocks adaptive resistance and synergizes with MEK inhibition for the treatment of NRAS-mutant melanoma.

Authors:  Joshua L D Parris; Thibaut Barnoud; Julia I-Ju Leu; Jessica C Leung; Weili Ma; Nicole A Kirven; Adi Naryana Reddy Poli; Andrew V Kossenkov; Qin Liu; Joseph M Salvino; Donna L George; Ashani T Weeraratna; Qing Chen; Maureen E Murphy
Journal:  Cancer Res Commun       Date:  2021-10
  1 in total

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