Division of Hematology, Mayo Clinic, Rochester, Minnesota.
Clin Adv Hematol Oncol. 2020 Jun;18(6):348-357.
The increased use of several effective novel targeted therapy agents has revolutionized therapy for patients with chronic lymphocytic leukemia (CLL). Disease progression in patients with CLL continues to occur, however. In particular, 3% to 25% of patients treated with a novel agent develop Richter transformation (RT); that is, histologic transformation of CLL to an aggressive lymphoma, most commonly diffuse large B-cell lymphoma (DLBCL). RT that develops in the novel agent era is frequently associated with adverse molecular alterations, such as TP53 disruption and complex karyotype. As a result, patients with RT in the era of novel agents typically have poor responses to the traditional chemotherapy used to treat de novo DLBCL. These patients also tend to have poor survival outcomes, with a median overall survival of less than 1 year. In this article, we review the contemporary literature of RT, particularly in the context of novel agents used for CLL, and discuss the management approach of RT in the novel agent era.
几种有效的新型靶向治疗药物的广泛应用彻底改变了慢性淋巴细胞白血病(CLL)患者的治疗方法。然而,CLL 患者的疾病仍会进展。特别是,接受新型药物治疗的患者中有 3%至 25%会发生 Richter 转化(RT),即 CLL 向侵袭性淋巴瘤的组织学转化,最常见的是弥漫性大 B 细胞淋巴瘤(DLBCL)。新型药物时代发生的 RT 常伴有不良的分子改变,如 TP53 缺失和复杂核型。因此,新型药物时代发生 RT 的患者对用于治疗初发性 DLBCL 的传统化疗通常反应不佳。这些患者的生存结局也较差,中位总生存期不到 1 年。本文综述了 RT 的当代文献,特别是在用于 CLL 的新型药物背景下,并讨论了新型药物时代 RT 的治疗方法。