Department of Haematology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Future Oncol. 2013 Sep;9(9):1283-98. doi: 10.2217/fon.13.134.
Rituximab is the first and most widely adopted anti-CD20 monoclonal antibody, and has dramatically improved outcomes for patients with B-cell malignancies. Rituximab is active as a single agent and when combined with chemotherapy improves both response rates and survival compared with chemotherapy alone. This approach has become standard of care in this setting. A number of Phase III studies using extended applications of rituximab have demonstrated that patients achieve a significantly longer progression-free survival, at the cost of an increase in infective complications. This has resulted in the widespread adoption of maintenance rituximab following the completion of primary therapy. Rituximab is useful in both previously untreated patients and at relapse, although a subset of patients develop disease that is rituximab resistant, which along with histologic transformation remains a significant management problem for patients with follicular lymphoma. The toxicities are modest and manageable, including infusion reactions, late-onset neutropenia, impaired humoral immunity, reactivation of hepatitis and possibly pulmonary toxicity.
利妥昔单抗是首个也是应用最广泛的抗 CD20 单克隆抗体,显著改善了 B 细胞恶性肿瘤患者的预后。利妥昔单抗作为单一药物具有活性,与化疗联合使用可提高反应率和生存率,优于单纯化疗。这种方法已成为该领域的标准治疗方法。多项扩展应用利妥昔单抗的 III 期研究表明,患者的无进展生存期显著延长,但感染并发症的风险增加。这导致在完成初始治疗后广泛采用维持性利妥昔单抗治疗。利妥昔单抗在初治患者和复发患者中均有效,尽管一部分患者出现了利妥昔单抗耐药的疾病,这与组织学转化仍然是滤泡性淋巴瘤患者的一个重大管理问题。其毒性适度且可管理,包括输注反应、迟发性中性粒细胞减少症、体液免疫受损、肝炎再激活,以及可能的肺毒性。