Emerging drugs for the treatment of cutaneous T-cell lymphoma

被引:16
作者
Cheng, Melissa [1 ,2 ]
Zain, Jasmine [3 ]
Rosen, Steven T. [3 ,4 ]
Querfeld, Christiane [1 ,4 ,5 ]
机构
[1] City Hope Natl Med Ctr, Div Dermatol, 1500 E Duarte Rd, Duarte, CA 91010 USA
[2] Western Univ Hlth Sci, Coll Ostepath Med Pacific, Pomona, CA USA
[3] City Hope Natl Med Ctr, Dept Hematol & Hematopoiet Cell Transplantat, 1500 E Duarte Rd, Duarte, CA 91010 USA
[4] Beckman Res Inst, Duarte, CA USA
[5] City Hope Natl Med Ctr, Dept Pathol, Duarte, CA 91010 USA
关键词
Cutaneous T cell lymphoma; CTCL; antagomir-155; anti-CCR4; anti-CD47; brentuximab-vedotin; cobomarsen; durvalumab; miRNA inhibitors; mogamulizumab; PD1; PD-L1; blockade; pembrolizumab; peptide inhibitors; TTI-621; KIR3DL2; MYCOSIS-FUNGOIDES; BRENTUXIMAB VEDOTIN; MONOCLONAL-ANTIBODY; CD30; EXPRESSION; SEZARY-SYNDROME; PHASE-2; TRIAL; OPEN-LABEL; THERAPY; LENALIDOMIDE; PATHOGENESIS;
D O I
10.1080/14728214.2022.2049233
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction Cutaneous T cell lymphoma (CTCL) is a rare and incurable group of non-Hodgkin lymphomas that manifest as patches, plaques, tumors, and/or erythroderma in the skin. Standard skin-directed therapies for CTCL are effective in patients with indolent early-stage disease, but more advanced/refractory stage patients require systemic therapies. However, none of the treatments are considered curative and most patients suffer from relapses. Biologic therapies and immunotherapy provide novel treatment options for patients with advanced or refractory disease. Areas covered This review provides a discussion of recently approved biological and novel therapeutics that are actively developed for the management of the heterogeneous group of CTCL. Expert opinion Mogamulizumab and brentuximab vedotin have reached the market and are approved for the treatment of CTCL, providing valuable options. Additionally, therapies utilizing immune checkpoint inhibitors, miRNA inhibitors, and peptide inhibitors show promising results in clinical trials. Durvalumab, pembrolizumab, TTI-621, BNZ-1, and MRG-106 are several of the emerging treatments still in trials. Further combinatorial studies are needed as none of the treatments have demonstrated long-term remissions.
引用
收藏
页码:45 / 54
页数:10
相关论文
共 68 条
[1]   Survival Outcomes and Prognostic Factors in Mycosis Fungoides/Sezary Syndrome: Validation of the Revised International Society for Cutaneous Lymphomas/European Organisation for Research and Treatment of Cancer Staging Proposal [J].
Agar, Nita Sally ;
Wedgeworth, Emma ;
Crichton, Siobhan ;
Mitchell, Tracey J. ;
Cox, Michael ;
Ferreira, Silvia ;
Robson, Alistair ;
Calonje, Eduardo ;
Stefanato, Catherine M. ;
Wain, Elizabeth Mary ;
Wilkins, Bridget ;
Fields, Paul A. ;
Dean, Alan ;
Webb, Katherine ;
Scarisbrick, Julia ;
Morris, Stephen ;
Whittaker, Sean J. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (31) :4730-4739
[2]  
[Anonymous], 2016, BLOOD
[3]   IPH4102, a first-in-class anti-KIR3DL2 monoclonal antibody, in patients with relapsed or refractory cutaneous T-cell lymphoma: an international, first-in-human, open-label, phase 1 trial [J].
Bagot, Martine ;
Porcu, Pierluigi ;
Marie-Cardine, Anne ;
Battistella, Maxime ;
William, Basem M. ;
Vermeer, Maarten ;
Whittaker, Sean ;
Rotolo, Federico ;
Ram-Wolff, Caroline ;
Khodadoust, Michael S. ;
Bensussan, Armand ;
Paturel, Carine ;
Bonnafous, Cecile ;
Sicard, Helene ;
Azim, Hatem A., Jr. ;
Kim, Youn H. .
LANCET ONCOLOGY, 2019, 20 (08) :1160-1170
[4]   First-in-Human, Multicenter Phase I Study of IPH4102, First-in-Class Humanized Anti-KIR3DL2 Monoclonal Antibody, in Relapsed/Refractory Cutaneous T-Cell Lymphomas: Preliminary Safety, Exploratory and Clinical Activity Results [J].
Bagot, Martine ;
Porcu, Pierluigi ;
Ram-Wolff, Caroline ;
Khodadoust, Michael ;
Battistella, Maxime ;
Marie-Cardine, Anne ;
Mathieu, Steve ;
Vermeer, Maarten H. ;
Whittaker, Sean ;
Duvic, Madeleine ;
Bensussan, Armand ;
Paturel, Carine ;
Bonnafous, Cecile ;
Thonnart, Nicolas ;
Widemann, Agnes ;
Bonin, Cecile ;
Sicard, Helene ;
Paiva, Christine ;
Pilz, Korinna ;
Kim, Youn .
BLOOD, 2016, 128 (22)
[5]   Sezary syndrome and mycosis fungoides arise from distinct T-cell subsets: a biologic rationale for their distinct clinical behaviors [J].
Campbell, James J. ;
Clark, Rachael A. ;
Watanabe, Rei ;
Kupper, Thomas S. .
BLOOD, 2010, 116 (05) :767-771
[6]  
Choe-Juliak C, 2020, J CLIN ONCOL, V38
[7]   Genomic landscape of cutaneous T cell lymphoma [J].
Choi, Jaehyuk ;
Goh, Gerald ;
Walradt, Trent ;
Hong, Bok S. ;
Bunick, Christopher G. ;
Chen, Kan ;
Bjornson, Robert D. ;
Maman, Yaakov ;
Wang, Tiffany ;
Tordoff, Jesse ;
Carlson, Kacie ;
Overton, John D. ;
Liu, Kristina J. ;
Lewis, Julia M. ;
Devine, Lesley ;
Barbarotta, Lisa ;
Foss, Francine M. ;
Subtil, Antonio ;
Vonderheid, Eric C. ;
Edelson, Richard L. ;
Schatz, David G. ;
Boggon, Titus J. ;
Girardi, Michael ;
Lifton, Richard P. .
NATURE GENETICS, 2015, 47 (09) :1011-+
[8]   Incidence of cutaneous T-Cell lymphoma in the United States, 1973-2002 [J].
Criscione, Vincent D. ;
Weinstock, Martin A. .
ARCHIVES OF DERMATOLOGY, 2007, 143 (07) :854-859
[9]   Brentuximab Vedotin [J].
Deng, Changchun ;
Pan, Beiqing ;
O'Connor, Owen A. .
CLINICAL CANCER RESEARCH, 2013, 19 (01) :22-27
[10]   Anti-pruritic properties of remetinostat (SHAPE), a topical histone deacetylase inhibitor (HDACi); data from a randomized phase 2 study in patients with stage IA-IIA mycosis fungoides [J].
Duvic, M. ;
Guitart, J. ;
Huen, A. ;
Porcu, P. ;
LeBoeuf, N. R. ;
Skolnik, J. ;
Owen, K. ;
Ohd, J. ;
Kim, Y. H. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2018, 138 (05) :S103-S103