Mucosal melanoma: from molecular landscape to current treatment strategies

被引:4
作者
Mattei, Jane [1 ,4 ]
Trindade, Eduardo N. [2 ]
Chedid, Marcio F. [2 ,3 ]
机构
[1] Univ Texas, Div Med Oncol, San Antonio, TX USA
[2] Univ Fed Rio Grande do Sul, Hosp Clin Porto Alegre, Div Gastrointestinal Surg & Liver Transplantat, Med Sch, Porto Alegre, Brazil
[3] Univ Fed Rio Grande do Sul, Med Sch, Hosp Clin Porto Alegre, Postgrad Program Surg Sci, Porto Alegre, Brazil
[4] Univ Texas, Div Med Oncol, 7979 Wurzbach Rd, MC 8232, San Antonio, TX 78229 USA
关键词
biochemotherapy; checkpoint inhibitors; imatinib; immunotherapy; mucosal melanoma; nivolumab; PD-1; pembrolizumab; target therapy; treatment; TUMOR-INFILTRATING LYMPHOCYTES; ADOPTIVE CELL THERAPY; METASTATIC MELANOMA; MALIGNANT-MELANOMA; KIT; IPILIMUMAB; EFFICACY; BIOCHEMOTHERAPY; MUTATIONS; OUTCOMES;
D O I
10.1097/CMR.0000000000000916
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mucosal melanoma (MM) is an aggressive tumor originating from melanocytes located in the respiratory, gastrointestinal, and urogenital tract with clinical and pathologic characteristics distinct from cutaneous melanoma. In addition, MMs have a unique biology that contributes to delayed diagnosis and, therefore an adverse prognosis. The factors all contribute to a treatment paradigm unique from its more studied cutaneous brethren. Due to the rarity of this disease, well-established protocols for the treatment of this pathology have yet to be established. The use of immune checkpoint inhibitors patterned after cutaneous melanoma has become the de facto primary therapeutic approach; however, cytotoxic strategies and pathway-targeted therapies have a defined role in treatment. Judicious use of these approaches can give rise to durable unmaintained disease responses.
引用
收藏
页码:447 / 453
页数:7
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