Department of Leukemia, The University of Texas M. D. Anderson Cancer Center, Unit 428, 1515 Holcombe Blvd, Houston, TX, 77030;
J Clin Oncol. 2010 Feb 10;28(5):884-92. doi: 10.1200/JCO.2009.22.8254. Epub 2010 Jan 4.
The use of rituximab-based chemoimmunotherapy regimens has remarkably improved the response rates, long-term outcomes, and quality of life of patients with B-cell malignancies. However, a substantial number of patients exhibit either primary or acquired resistance to rituximab, which suggests that novel immunotherapeutics with distinct mechanisms of action are necessary. A series of monoclonal antibodies with specificity against different surface antigens expressed on malignant B cells (eg, CD22, CD23, CD40, CD70) and novel immunotherapeutics (eg, bispecific monoclonal antibodies, small-modular immunopharmaceuticals, T-cell engagers) are currently in clinical or final preclinical stages of development. Although these agents offer reason for optimism, considerable challenges lie ahead in establishing their real clinical value, as well as in integrating them into current therapeutic algorithms for patients with B-cell malignancies. This review describes some of the most promising investigational immunotherapeutics for the treatment of B-cell malignancies.
基于利妥昔单抗的化疗免疫治疗方案的使用显著提高了 B 细胞恶性肿瘤患者的反应率、长期预后和生活质量。然而,相当数量的患者对利妥昔单抗表现出原发性或获得性耐药,这表明需要具有不同作用机制的新型免疫疗法。一系列针对恶性 B 细胞上表达的不同表面抗原(例如 CD22、CD23、CD40、CD70)的特异性单克隆抗体和新型免疫疗法(例如双特异性单克隆抗体、小模块化免疫药物、T 细胞衔接器)目前处于临床或最终临床前开发阶段。尽管这些药物令人乐观,但在确定它们的真正临床价值以及将其整合到当前 B 细胞恶性肿瘤患者的治疗方案中方面,仍然存在相当大的挑战。本文综述了一些最有前途的用于治疗 B 细胞恶性肿瘤的研究性免疫疗法。