The role of systemic therapy in melanoma brain metastases: a narrative review

被引:2
|
作者
Saleem, Kainat [1 ]
Davar, Diwakar [1 ,2 ]
机构
[1] Univ Pittsburgh, Dept Med, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, UPMC Ilillman Canc Ctr, Pittsburgh, PA 15213 USA
关键词
Melanoma; melanoma brain metastases (MBM); immunotherapy; targeted therapy; immune checkpoint inhibitors (ICI); programmed death-1 (PD-1); CTLA-4; BRAF; MEK; TUMOR-INFILTRATING LYMPHOCYTES; MUTATION-POSITIVE MELANOMA; CTLA-4; COUNTER-RECEPTOR; CENTRAL-NERVOUS-SYSTEM; OPEN-LABEL; MEK INHIBITION; COMBINED NIVOLUMAB; LEPTOMENINGEAL DISEASE; PROGNOSTIC-FACTORS; RADIATION-THERAPY;
D O I
10.21037/cco-22-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and Objective: Melanoma is a disease notorious for the development of brain metastases, with consequently poor outcomes for patients who develop melanoma brain metastases (MBM). The treatment options for patients with MBM were limited to radiotherapy and surgery. MBM patients, particularly those with symptomatic disease, were excluded from clinical trials of immune checkpoint inhibitors (ICI) and BRAF/MEK inhibitors. Recent post-approval studies have, demonstrated important roles for existing systemic ICIs and BRAF/MEK inhibitors in untreated MBM, dramatically altering the landscape of melanoma patients in general and MBM in particular. These trials have also identified key areas for which more effective strategies are needed including: symptomatic MBM, and leptomeningeal disease (LMD). Methods: PubMed, Scopus, Embase, and Embase databases were systematically queried to obtain records pertaining to the etiology of and treatment for MBM. Clinical trial databases were reviewed to obtain details regarding MBM clinical trials. Key Content and Findings: We discuss the etiopathogenesis of MBM and the novel immune, molecular and metabolic features of MBM that make this disease a unique therapeutic challenge. We review advances in systemic therapy with ICIs and BRAF/MEK inhibitors in untreated MBM, along with novel combinations. Finally, we debate challenging situations such as LMD, and delineate novel treatments and new paradigms for therapeutic interventions. Conclusions: The historically poor outcomes for MBM patients have been transformed with the advent of effective systemic therapies including ICIs and BRAF/MEK inhibitors. An improved understanding of the molecular and immunogenomic characterization of MBMs has provided new targets that are being exploited in the clinic.
引用
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页数:20
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