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.
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Univ Utah, Dept Oncol Sci, Salt Lake City, UT USAUniv Utah, Dept Oncol Sci, Salt Lake City, UT USA
Weaver, Bradley D.
Goodman, James R.
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Oregon Hlth & Sci Univ, Dept Anesthesiol & Perioperat Meidcine, Portland, OR 97201 USA
Oregon Hlth & Sci Univ, Dept Physiol & Pharmacol, Portland, OR 97201 USAUniv Utah, Dept Oncol Sci, Salt Lake City, UT USA
Goodman, James R.
Jensen, Randy
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Univ Utah, Dept Neurosurg, Salt Lake City, UT 84112 USAUniv Utah, Dept Oncol Sci, Salt Lake City, UT USA
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Queens Univ, Dept Radiat Oncol, Kingston, ON, Canada
Harvard Med Sch, Massachusetts Gen Hosp, Ctr Canc, Div Hematol Oncol,Dept Med, Boston, MA USAQueens Univ, Dept Radiat Oncol, Kingston, ON, Canada
Brastianos, Harry C.
Cahill, Daniel P.
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Harvard Med Sch, Massachusetts Gen Hosp, Dept Neurosurg, Boston, MA USAQueens Univ, Dept Radiat Oncol, Kingston, ON, Canada
Cahill, Daniel P.
Brastianos, Priscilla K.
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Harvard Med Sch, Stephen E & Catherine Pappas Ctr Neurooncol, Div Neurooncol, 55 Fruit St,Yawkey 9E, Boston, MA 02114 USAQueens Univ, Dept Radiat Oncol, Kingston, ON, Canada
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Royal Marsden NHS Fdn Trust, Paediat & Adolescent Drug Dev Team, Downs Rd, London SM2 5PT, England
Inst Canc Res, London, EnglandRoyal Marsden NHS Fdn Trust, Paediat & Adolescent Drug Dev Team, Downs Rd, London SM2 5PT, England
Corley, Elizabeth A.
Schmitt, Andreas M.
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Royal Marsden NHS Fdn Trust, Renal & Skin Unit, London, EnglandRoyal Marsden NHS Fdn Trust, Paediat & Adolescent Drug Dev Team, Downs Rd, London SM2 5PT, England
Schmitt, Andreas M.
Furness, Andrew J. S.
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Inst Canc Res, London, England
Royal Marsden NHS Fdn Trust, Renal & Skin Unit, London, England
Royal Marsden, NIHR Biomed Res Ctr, London, EnglandRoyal Marsden NHS Fdn Trust, Paediat & Adolescent Drug Dev Team, Downs Rd, London SM2 5PT, England
Furness, Andrew J. S.
Chisholm, Julia C.
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Royal Marsden NHS Fdn Trust, Paediat & Adolescent Drug Dev Team, Downs Rd, London SM2 5PT, England
Inst Canc Res, London, EnglandRoyal Marsden NHS Fdn Trust, Paediat & Adolescent Drug Dev Team, Downs Rd, London SM2 5PT, England
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NCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, JapanNCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, Japan
Yamazaki, N.
Wada, S.
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NCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, JapanNCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, Japan
Wada, S.
Ogata, D.
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NCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol, Chuo Ku, Tokyo, JapanNCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, Japan
Ogata, D.
Nakano, E.
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NCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, JapanNCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, Japan
Nakano, E.
Kashihara, T.
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NCCH Natl Canc Ctr Hosp Tsukiji Campus, Radiat Oncol, Chuo Ku, Tokyo, JapanNCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, Japan
Kashihara, T.
Okuma, K.
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NCCH Natl Canc Ctr Hosp Tsukiji Campus, Radiat Oncol, Chuo Ku, Tokyo, JapanNCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, Japan
Okuma, K.
Eto, H.
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NCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, JapanNCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, Japan
Eto, H.
Takahashi, A.
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Natl Canc Ctr Hosp East, Dermatol Oncol, Kashiwa, Chiba, JapanNCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, Japan
Takahashi, A.
Igaki, H.
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NCCH Natl Canc Ctr Hosp, Radiat Oncol, Chuo Ku, Tokyo, JapanNCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, Japan
Igaki, H.
Namikawa, K.
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NCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, JapanNCCH Natl Canc Ctr Hosp Tsukiji Campus, Dermatol Oncol, Chuo Ku, Tokyo, Japan