What is the best salvage therapy for Hodgkin lymphoma?

被引:0
作者
Luttwak, Efrat [1 ]
Moskowitz, Alison J. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Lymphoma Serv, 530 East 74th St, New York, NY 10021 USA
关键词
high dose chemotherapy and autologous stem cell transplant; Hodgkin lymphoma; programmed death-1; relapsed/refractory; salvage chemotherapy; STEM-CELL TRANSPLANTATION; POSITRON-EMISSION-TOMOGRAPHY; HIGH-DOSE CHEMOTHERAPY; BRENTUXIMAB VEDOTIN; FDG-PET; PROGNOSTIC-SIGNIFICANCE; GEMCITABINE; NIVOLUMAB; 2ND-LINE; DISEASE;
D O I
10.1097/CCO.0000000000001073
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of reviewHistorically, salvage chemotherapy followed by high-dose chemotherapy and autologous stem cell transplant (HDT/ASCT) was the mainstay approach for relapsed or refractory classic HL. The emergence of novel agents for HL, such as brentuximab vedotin and programmed death-1 (PD-1) blockade has revolutionized therapeutic strategies, yielding excellent results. This review aims to provide a comprehensive overview of new salvage therapies and offer insights into forthcoming therapeutic options.Recent findingsThe incorporation of brentuximab vedotin and PD-1 blockade into salvage therapy before HDT/ASCT has led to markedly improved outcomes. Notably, PD-1 based salvage studies yield posttransplant 2-year progression-free survival rates approaching 90%, marking a significant advancement in the treatment of Hodgkin lymphoma (HL). Studies are beginning to explore nontransplant treatment approaches following front-line treatment failure and may identify certain risk groups eligible for these strategies.SummaryThe landscape of HL treatment is rapidly evolving, leading to significant changes in the standard of care. Novel agents are now administered earlier in the disease course, resulting in higher cure rates. The focus of treatment is shifting towards achieving cure with minimal toxicity, reducing exposure to various agents, and advancing research in optimizing treatment sequencing and patient selection for less intensive therapies.
引用
收藏
页码:346 / 352
页数:7
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