Recent advances in therapeutic strategies for unresectable or metastatic melanoma and real-world data in Japan.
Antineoplastic Agents
/ therapeutic use
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Brain Neoplasms
/ secondary
Humans
Immunotherapy
/ methods
Japan
/ epidemiology
Melanoma
/ epidemiology
Molecular Targeted Therapy
/ methods
Mutation
Programmed Cell Death 1 Receptor
/ antagonists & inhibitors
Protein Kinase Inhibitors
/ therapeutic use
Proto-Oncogene Proteins B-raf
/ genetics
BRAF inhibitors
Biomarker
Immune checkpoint inhibitors
Japan
MEK inhibitors
Melanoma
Journal
International journal of clinical oncology
ISSN: 1437-7772
Titre abrégé: Int J Clin Oncol
Pays: Japan
ID NLM: 9616295
Informations de publication
Date de publication:
Dec 2019
Dec 2019
Historique:
received:
10
01
2018
accepted:
17
01
2018
pubmed:
23
2
2018
medline:
23
2
2020
entrez:
23
2
2018
Statut:
ppublish
Résumé
New therapeutic strategies including immunotherapy and selective molecular target inhibitors have brought about a new era in the treatment of patients with advanced melanoma. In Japan, the immune checkpoint inhibitors ipilimumab, nivolumab and pembrolizumab, the BRAF inhibitor (BRAFi) vemurafenib, dabrafenib and MEK inhibitor (MEKi) trametinib have been available for the treatment of unresectable and metastatic melanoma. The BRAFi + MEKi combination shows high response rates (60-70%) and rapid response induction associated with symptom control, with a progression-free survival of 12 months. Nivolumab and pembrolizumab offer moderate response rates (30-40%) and long survival (3- to 5-year survival: 30-50%). In Japan, treatment options for the first-line setting frequently include nivolumab or pembrolizumab monotherapy and BRAFi + MEKi combinations (for patients with BRAF-mutant melanoma). Ipilimumab is included in the second-line setting, and the nivolumab + ipilimumab combination has not been approved yet in Japan. Although these medications have demonstrated impressive efficacy, the clinical trials and real-world data have shown that the clinical benefit is not fully satisfactory. We have to carefully manage a new class of adverse events due to these medicines. Moreover, biomarkers are emerging with which we can identify a population that would experience more benefits without severe adverse events.
Identifiants
pubmed: 29470725
doi: 10.1007/s10147-018-1246-y
pii: 10.1007/s10147-018-1246-y
doi:
Substances chimiques
Antineoplastic Agents
0
PDCD1 protein, human
0
Programmed Cell Death 1 Receptor
0
Protein Kinase Inhibitors
0
BRAF protein, human
EC 2.7.11.1
Proto-Oncogene Proteins B-raf
EC 2.7.11.1
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
1508-1514Subventions
Organisme : Japan Society for the Promotion of Science
ID : JP16K10150
Références
J Dermatol Sci. 2018 Jan;89(1):60-66
pubmed: 29079332
N Engl J Med. 2010 Aug 19;363(8):711-23
pubmed: 20525992
Lancet. 2014 Sep 20;384(9948):1109-17
pubmed: 25034862
J Clin Oncol. 2006 Sep 10;24(26):4340-6
pubmed: 16908931
Ann Oncol. 2017 Jul 01;28(7):1631-1639
pubmed: 28475671
Lancet Oncol. 2017 Jul;18(7):863-873
pubmed: 28592387
Clin Transl Oncol. 2018 Feb;20(2):169-175
pubmed: 28674996
N Engl J Med. 2015 Jul 2;373(1):23-34
pubmed: 26027431
N Engl J Med. 2012 Nov;367(18):1694-703
pubmed: 23020132
Jpn J Clin Oncol. 2016 Jan;46(1):86-8
pubmed: 26491202
Science. 2015 Oct 9;350(6257):207-211
pubmed: 26359337
Oncoimmunology. 2016 Jun 30;5(9):e1204507
pubmed: 27757299
Lancet Oncol. 2015 Apr;16(4):375-84
pubmed: 25795410
Int J Clin Oncol. 2016 Oct;21(5):981-988
pubmed: 27041702
J Clin Oncol. 2015 Jun 10;33(17):1889-94
pubmed: 25667295
N Engl J Med. 2012 Jun 28;366(26):2443-54
pubmed: 22658127
Lancet. 2015 Aug 1;386(9992):444-51
pubmed: 26037941
Lancet Oncol. 2015 May;16(5):522-30
pubmed: 25840693
J Clin Oncol. 2014 Apr 1;32(10):1020-30
pubmed: 24590637
N Engl J Med. 2017 Nov 9;377(19):1824-1835
pubmed: 28891423
J Clin Oncol. 2018 Jun 10;36(17):1658-1667
pubmed: 28981385
N Engl J Med. 2017 Nov 9;377(19):1813-1823
pubmed: 28891408
BMC Med. 2015 Sep 04;13:211
pubmed: 26337719
Cell. 2015 Jun 18;161(7):1681-96
pubmed: 26091043
J Invest Dermatol. 1998 Nov;111(5):757-61
pubmed: 9804334
Br J Cancer. 2012 Feb 28;106(5):939-46
pubmed: 22281663
J Dermatol Sci. 2017 Nov;88(2):225-231
pubmed: 28736218
Clin Cancer Res. 2016 Feb 15;22(4):886-94
pubmed: 26446948
Ann Oncol. 2016 Mar;27(3):546-7
pubmed: 26602778
Diabetes Care. 2015 Apr;38(4):e55-7
pubmed: 25805871
Lancet Oncol. 2016 Dec;17(12):1743-1754
pubmed: 27864013
N Engl J Med. 2017 Oct 5;377(14):1345-1356
pubmed: 28889792
Ann Oncol. 2017 Oct 01;28(10):2377-2385
pubmed: 28945858
Melanoma Res. 2017 Aug;27(4):358-368
pubmed: 28509765
Oncotarget. 2016 Nov 22;7(47):77404-77415
pubmed: 27764805
N Engl J Med. 2011 Jun 30;364(26):2517-26
pubmed: 21639810
Int J Clin Oncol. 2014;19(3):544-8
pubmed: 23739925
N Engl J Med. 2005 Nov 17;353(20):2135-47
pubmed: 16291983
J Dermatol Sci. 2008 Jun;50(3):185-96
pubmed: 18226503
J Clin Oncol. 2018 Mar 1;36(7):667-673
pubmed: 28991513
Clin Cancer Res. 2012 Jun 15;18(12):3242-9
pubmed: 22535154
N Engl J Med. 2015 Jun 25;372(26):2521-32
pubmed: 25891173
Ann Oncol. 2016 Mar;27(3):434-41
pubmed: 26712903
J Dermatol Sci. 2015 Oct;80(1):33-7
pubmed: 26282084
Nature. 2017 May 11;545(7653):175-180
pubmed: 28467829
Neurology. 2017 Sep 12;89(11):1127-1134
pubmed: 28821685
Ann Oncol. 2016 Jul;27(7):1199-206
pubmed: 27122549