Davis T A, Czerwinski D K, Levy R
National Cancer Institute, NIH, Rockville, Maryland 20852, USA.
Clin Cancer Res. 1999 Mar;5(3):611-5.
Rituximab is a chimeric antibody with human gamma-1 and kappa constant regions and murine variable regions. It recognizes the CD20 antigen, a pan B-cell marker. Therapeutic trials in patients with B-cell non-Hodgkin's lymphoma (NHL) have shown significant efficacy with a primary response rate of 50%, and a secondary response rate of 44% after repeat treatments in prior responders. The selection for proliferating tumor cells that no longer express CD20 may compromise repeated treatment. We have identified a patient who developed a transformed NHL that lost CD20 protein expression after two courses of therapy with rituximab. In a pretreatment lymph node biopsy, 83% of B cells (as defined by CD19 and surface immunoglobulin) expressed surface CD20. A biopsy from the recurrent tumor after two courses of rituximab revealed a diffuse large cell NHL where 0% of B cells expressed CD20 with no evidence of bound rituximab. Cytoplasmic staining showed no CD20 protein. Sequencing of immunoglobulin heavy chain cDNA identified identical variable sequences in the initial and recurrent lymphomas, confirming the association between the two tumors. Literature and database review suggests that approximately 98% of diffuse large cell lymphomas express CD20, which suggests that these tumors rarely survive without CD20. This is the first identified case of loss of CD20 expression in a lymphoma that has relapsed after rituximab therapy, although several other cases have since been identified. Considering the significant number of patients treated with anti-CD20 antibodies, this may occur only rarely and is unlikely to preclude recurrent therapy with anti-CD20 antibodies in the majority of patients. However, because many patients have relapsed after anti-CD20 antibody therapy and have not been biopsied to identify clones with down-regulated CD20 antigen, we do not currently know the true frequency of this phenomenon. When possible, patients should undergo evaluation for CD20 expression before repeated courses of anti-CD20 therapy.
利妥昔单抗是一种嵌合抗体,具有人γ-1和κ恒定区以及鼠可变区。它识别CD20抗原,这是一种泛B细胞标志物。对B细胞非霍奇金淋巴瘤(NHL)患者的治疗试验显示出显著疗效,初次缓解率为50%,先前有反应的患者在重复治疗后的二次缓解率为44%。选择不再表达CD20的增殖肿瘤细胞可能会影响重复治疗。我们发现了一名患者,在接受两疗程利妥昔单抗治疗后发生了转化型NHL,其失去了CD20蛋白表达。在预处理的淋巴结活检中,83%的B细胞(由CD19和表面免疫球蛋白定义)表达表面CD20。两疗程利妥昔单抗治疗后的复发肿瘤活检显示为弥漫性大细胞NHL,其中0%的B细胞表达CD20,且没有利妥昔单抗结合的证据。细胞质染色未显示CD20蛋白。免疫球蛋白重链cDNA测序在初始和复发淋巴瘤中鉴定出相同的可变序列,证实了这两个肿瘤之间的关联。文献和数据库回顾表明,大约98%的弥漫性大细胞淋巴瘤表达CD20,这表明这些肿瘤在没有CD20的情况下很少存活。这是首次发现的利妥昔单抗治疗后复发的淋巴瘤中CD20表达缺失的病例,尽管此后又发现了其他几例。考虑到接受抗CD20抗体治疗的患者数量众多,这种情况可能很少发生,并且不太可能排除大多数患者使用抗CD20抗体进行复发治疗。然而,由于许多患者在抗CD20抗体治疗后复发且未进行活检以鉴定CD20抗原下调的克隆,我们目前尚不知道这种现象的真实发生率。可能的话,患者在接受重复疗程的抗CD20治疗前应进行CD20表达评估。