How I incorporate novel agents into the treatment of classical Hodgkin lymphoma

被引:7
|
作者
Epperla, Narendranath [1 ,2 ]
Herrera, Alex F. [3 ]
机构
[1] Ohio State Univ, James Canc Hosp, Div Hematol, Columbus, OH 43210 USA
[2] Ohio State Univ, Solove Res Inst, Columbus, OH 43210 USA
[3] City Hope Natl Med Ctr, Dept Hematol & Hematopoiet Cell Transplantat, 1500 E Duarte Rd, Duarte, CA 91010 USA
关键词
STEM-CELL TRANSPLANTATION; EMISSION-TOMOGRAPHY RESPONSE; HIGH-DOSE CHEMOTHERAPY; BRENTUXIMAB VEDOTIN; SINGLE-ARM; STAGE-III; PHASE-II; ADAPTED TREATMENT; 2ND-LINE THERAPY; INTERGROUP TRIAL;
D O I
10.1182/blood.2020007900
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The introduction of targeted immunotherapies specifically, brentuximab vedotin (BV) and programmed death-1 (PD-1)-blocking antibodies (nivolumab and pembrolizumab), has reshaped the therapeutic landscape of classical Hodgkin lymphoma (cHL) in the past decade. Targeting specific biologic features of cHL, these novel agents have expanded treatment options for patients with multiply R/R cHL and have increasingly been studied at earlier points in a patient's disease course. With the plethora of studies evaluating BV and PD-1 blockade as part of cHL therapy, often in nonrandomized, controlled studies, more questions than answers have arisen about how to optimally integrate these drugs into clinical practice. In this article, we use a case-based format to offer practical guidance on how we incorporate BV and anti-PD-1 antibodies into the management of cHL and review the data supporting those recommendations.
引用
收藏
页码:520 / 530
页数:11
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