Khodadoust Michael S, Mou Eric, Kim Youn H
Division of Oncology, Stanford University, Stanford, CA.
Department of Dermatology, Stanford University, Stanford, CA.
Blood. 2023 Feb 16;141(7):695-703. doi: 10.1182/blood.2020008241.
Agents targeting the unique biology of mycosis fungoides and Sézary syndrome are quickly being incorporated into clinical management. With these new therapies, we are now capable of inducing more durable responses and even complete remissions in advanced disease, outcomes which were exceedingly rare with prior therapies. Yet, even this new generation of therapies typically produce objective responses in only a minority of patients. As our therapeutic options increase, we are now challenged with selecting treatments from a growing list of options. To gain the full benefit of these novel agents, we must develop strategies to match treatments for the patients most likely to benefit from them. Here, we consider both the current approaches to treatment selection based on clinical features and the future of molecular biomarker-guided therapy for patients with this heterogeneous disease.
针对蕈样肉芽肿和 Sézary 综合征独特生物学特性的药物正迅速被纳入临床管理。有了这些新疗法,我们现在能够在晚期疾病中诱导出更持久的反应,甚至实现完全缓解,而这些结果在以前的治疗中极为罕见。然而,即使是这新一代疗法通常也仅在少数患者中产生客观反应。随着我们的治疗选择增多,我们现在面临着从越来越多的选项中选择治疗方法的挑战。为了充分利用这些新型药物,我们必须制定策略,为最有可能从中受益的患者匹配治疗方法。在此,我们既考虑了基于临床特征的当前治疗选择方法,也探讨了针对这种异质性疾病患者的分子生物标志物导向治疗的未来发展。