Vassilakopoulos Theodoros P, Asimakopoulos John V, Konstantopoulos Kostas, Angelopoulou Maria K
Department of Haematology and Bone Marrow Transplantation, National and Kapodistrian University of Athens, School of Medicine, Laikon General Hospital, 17 Ag. Thoma Str., Goudi, Athens, 11527, Greece.
Department of Haematology and Bone Marrow Transplantation, National and Kapodistrian University of Athens, Laikon General Hospital, Athens, Greece.
Ther Adv Hematol. 2020 Feb 16;11:2040620720902911. doi: 10.1177/2040620720902911. eCollection 2020.
The outcome of patients with relapsed/refractory classical Hodgkin lymphoma (rr-cHL) has improved considerably in recent years owing to the approval of highly active novel agents such as brentuximab vedotin and Programmed Death-1 (PD-1) inhibitors. Although no randomized trials have been conducted to provide formal proof, it is almost undisputable that the survival of these patients has been prolonged. As autologous stem-cell transplantation (SCT) remains the standard of care for second-line therapy of most patients with rr-cHL, optimization of second-line regimens with the use of brentuximab vedotin, or, in the future, checkpoint inhibitors, is promising to increase both the eligibility rate for transplant and the final outcome. The need for subsequent therapy, and especially allogeneic SCT, can be reduced with brentuximab vedotin consolidation for 1 year, while pembrolizumab is also being tested in this setting. Several other drug categories appear to be active in rr-cHL, but their development has been delayed by the appearance of brentuximab vedotin, nivolumab and pembrolizumab, which have dominated the field of rr-cHL treatment in the last 5 years. Combinations of active drugs in chemo-free approaches may further increase efficacy and hopefully reduce toxicity in rr-cHL, but are still under development.
近年来,由于诸如本妥昔单抗和程序性死亡-1(PD-1)抑制剂等高效新型药物的获批,复发/难治性经典型霍奇金淋巴瘤(rr-cHL)患者的预后有了显著改善。尽管尚未进行随机试验来提供正式证据,但这些患者的生存期得以延长几乎是无可争议的。由于自体干细胞移植(SCT)仍是大多数rr-cHL患者二线治疗的标准疗法,使用本妥昔单抗或未来使用检查点抑制剂优化二线治疗方案有望提高移植的适合率和最终疗效。本妥昔单抗巩固治疗1年可减少后续治疗的需求,尤其是异基因SCT的需求,同时派姆单抗也正在该治疗背景下进行试验。其他几类药物似乎对rr-cHL有活性,但它们的研发因本妥昔单抗、纳武单抗和派姆单抗的出现而延迟,这三种药物在过去5年里主导了rr-cHL的治疗领域。无化疗方案中活性药物的联合应用可能会进一步提高疗效,并有望降低rr-cHL的毒性,但仍在研发中。