Lee Yuna, Kyung Sun Young, Choi Soo Jin, Bang Soo-Mee, Jeong Seong Hwan, Shin Dong Bok, Lee Jae Hoon
Department of Internal Medicine, Gachon Medical School, Gil Medical Center, Incheon, Korea.
Korean J Intern Med. 2006 Sep;21(3):183-6. doi: 10.3904/kjim.2006.21.3.183.
Rituximab, a chimeric monoclonal antibody directed against CD20, has become a part of the standard therapy for patients with non-Hodgkin's lymphoma either in combination with other drugs or as a single agent. The CD20 antigen is expressed on 95% of B-cell lymphoma cells and normal B-cells but, is not found on precursor B-cells or stem cells. Rituximab is now approved for patients with diffuse large B-cell lymphoma when combined with standard CHOP chemotherapy (cyclophosphamide, doxorubicin, vincristine and prednisone) or patients with follicular lymphoma who have failed first line chemotherapy. The monoclonal antibody is generally well tolerated. Most of the adverse events are infusion-associated, mild to moderate non-hematological toxicities. Severe respiratory adverse events have been infrequent. Here, we report two patients with non-Hodgkin's lymphoma in whom interstitial pneumonitis developed with rituximab therapy.
利妥昔单抗是一种针对CD20的嵌合单克隆抗体,已成为非霍奇金淋巴瘤患者标准治疗方案的一部分,可与其他药物联合使用或作为单一药物使用。CD20抗原在95%的B细胞淋巴瘤细胞和正常B细胞上表达,但在前体B细胞或干细胞上未发现。利妥昔单抗目前已被批准用于弥漫性大B细胞淋巴瘤患者,与标准CHOP化疗(环磷酰胺、多柔比星、长春新碱和泼尼松)联合使用,或用于一线化疗失败的滤泡性淋巴瘤患者。该单克隆抗体通常耐受性良好。大多数不良事件与输液相关,为轻度至中度非血液学毒性。严重的呼吸道不良事件并不常见。在此,我们报告两名非霍奇金淋巴瘤患者,他们在接受利妥昔单抗治疗时发生了间质性肺炎。