Resistance to mogamulizumab is associated with loss of CCR4 in cutaneous T-cell lymphoma

被引:30
作者
Beygi, Sara [1 ]
Duran, George E. [1 ,2 ]
Fernandez-Pol, Sebastian [3 ]
Rook, Alain H. [4 ]
Kim, Youn H. [1 ,2 ]
Khodadoust, Michael S. [1 ,2 ]
机构
[1] Stanford Univ, Dept Med, Div Oncol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Dermatol, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Pathol, Stanford, CA 94305 USA
[4] Univ Penn, Dept Dermatol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
MYCOSIS-FUNGOIDES; SEZARY-SYNDROME;
D O I
10.1182/blood.2021014468
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mogamulizumab is a humanized anti-CC chemokine receptor 4 (CCR4) antibody approved for the treatment of mycosis fungoides and Sezary syndrome. Despite almost universal expression of CCR4 in these diseases, most patients eventually develop resistance to mogamulizumab. We tested whether resistance to mogamulizumab is associated with loss of CCR4 expression. We identified 17 patients with mycosis fungoides or Sezary syndrome who either were intrinsically resistant or acquired resistance to mogamulizumab. Low expression of CCR4 by immunohistochemistry or flow cytometry was found in 65% of patients. Novel emergent CCR4 mutations targeting the N-terminal and transmembrane domains were found in 3 patients after disease progression. Emerging CCR4 copy number loss was detected in 2 patients with CCR4 mutations. Acquisition of CCR4 genomic alterations corresponded with loss of CCR4 antigen expression. We also report on outcomes of 3 cutaneous T-cell lymphoma (CTCL) patients with gain-of-function CCR4 mutations treated with mogamulizumab. Our study indicates that resistance to mogamulizumab in CTCL frequently involves loss of CCR4 expression and emergence of CCR4 genomic alterations. This finding has implications for management and monitoring of CTCL patients on mogamulizumab and development of future CCR4-directed therapies.
引用
收藏
页码:3732 / 3736
页数:5
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