Ghielmini M, Schmitz S F, Bürki K, Pichert G, Betticher D C, Stupp R, Wernli M, Lohri A, Schmitter D, Bertoni F, Cerny T
Istituto Oncologico della Svizzera Italiana, Deparment of Medical Oncology, Lugano, Switzerland.
Ann Oncol. 2000;11 Suppl 1:123-6.
Clinical activity of the anti CD-20 monoclonal antibody Rituximab has been reported in patients with follicular lymphoma (FL) and mantle-cell lymphoma (MCL).
120 patients with bi-dimensionally measurable FL or MCL (R.E.A.L. Classification) were treated with Rituximab 375 mg/m2/week for 4 weeks. A central pathology review confirmed the diagnosis of FL in 76 of 78 and of MCL in 39 of 42 cases. The response was evaluated after 8 weeks and confirmed after 12 weeks from the start of treatment.
The toxicity of the treatment was, as expected, grade 1-2 fever and rigors during the first infusion and mild asthenia during the treatment period. Serious adverse events, probably or possibly related to the study treatment, included four deaths (3 of cardiac origin, 1 caused by P. carinii pneumonia) and 10 further nonfatal cases, including a permanent agranulocytosis and one case of heart failure. Response rate at week 12 was 52% for FL and 22% for MCL. After treatment, the BCL-2 rearrangement disappeared in 15 of 29 blood but only in 5 of 23 bone marrow samples; BCL-1 disappeared in 5 of 12 blood and 0 of 7 bone marrow specimens, as determined by PCR.
Rituximab is an active agent for the treatment of FL, while its efficacy is modest in MCL. The effect in reducing minimal residual disease is more pronounced on the blood than it is on the bone marrow.
抗CD-20单克隆抗体利妥昔单抗在滤泡性淋巴瘤(FL)和套细胞淋巴瘤(MCL)患者中的临床活性已有报道。
120例二维可测量的FL或MCL(REAL分类)患者接受利妥昔单抗375mg/m²/周治疗,共4周。中心病理复查确诊78例中的76例为FL,42例中的39例为MCL。治疗开始8周后评估反应,并在12周后确认。
治疗毒性如预期,首次输注期间为1-2级发热和寒战,治疗期间为轻度乏力。可能或可能与研究治疗相关的严重不良事件包括4例死亡(3例心脏原因,1例由卡氏肺孢子虫肺炎引起)和10例其他非致命病例,包括1例永久性粒细胞缺乏症和1例心力衰竭。第12周时FL的缓解率为52%,MCL为22%。治疗后,通过PCR检测,29份血液样本中的15份以及23份骨髓样本中的5份BCL-2重排消失;12份血液样本中的5份以及7份骨髓样本中的0份BCL-1消失。
利妥昔单抗是治疗FL的有效药物,而其在MCL中的疗效一般。其在减少微小残留病方面对血液的作用比对骨髓更明显。