Rasheed Afshan Asghar, Samad Adeel, Raheem Ahmed, Hirani Samina Ismail, Shabbir- Moosajee Munira
Department of Oncology, Section of Medical Oncology, the Aga Khan University Hospital, Karachi, Pakistan. Email:
Asian Pac J Cancer Prev. 2018 Feb 26;19(2):331-335. doi: 10.22034/APJCP.2018.19.2.331.
Introduction: Down regulation of CD20 expression has been reported in diffuse large B cell lymphoma (DLBCL)). Therefore, it is important to determine whether chemotherapy with rituximab induces CD20 down regulation and effects survival. Objectives: To determine the incidence of down regulation of CD20 expression in relapsed DLBCL after treatment with rituximab and to compare outcomes and assess pattern of relapse between CD20 negative and CD20 positive cases. Methodology: We retrospectively reviewed patients with relapsed DLBCL who received rituximab in the first line setting at Aga Khan University Hospital between January 2007 and December 2014. Data were recorded on predesigned questionnaires, with variables including demographics, details regarding date of diagnosis and relapse, histology, staging, international prognostic index, treatment and outcomes at initial diagnosis and at relapse. The Chi square test was applied to determine statistical significance between categorical variables. Survival curves were generated by the Kaplan–Meier method. Results: A total of 54 patients with relapsed DLBCL were included in our study, 38 (70 %) males and 16(30%) females. Some 23 (43%) patients were at stage IV at the time of diagnosis and 34 (63%) had B symptoms. The most frequent R-IPI at diagnosis was II in 24 (44%) patients. Only 6 (11%) did not show CD20 expression on re-biopsy for relapsed/refractory disease, 2 with CD20 negative DLBCL responding to second line chemotherapy. A complete response after salvage chemotherapy was noted in 16 (29.6%) cases with relapsed/refractory DLBCL. Seven (13%) patients underwent an autologous bone marrow transplant as consolidation after second line treatment. Median overall survival was 18 months in CD20 positive vs. 13 months in CD20 negative patients. Conclusion: This study demonstrated that a small percentage of patients treated with rituximab lose their CD20 expression at the time of relapse. However, it is unclear whether this is associated with an inferior outcome.
据报道,弥漫性大B细胞淋巴瘤(DLBCL)中CD20表达下调。因此,确定利妥昔单抗化疗是否会诱导CD20下调并影响生存率很重要。目的:确定利妥昔单抗治疗后复发的DLBCL中CD20表达下调的发生率,并比较CD20阴性和CD20阳性病例的预后及评估复发模式。方法:我们回顾性分析了2007年1月至2014年12月在阿迦汗大学医院一线接受利妥昔单抗治疗的复发DLBCL患者。数据记录在预先设计的问卷上,变量包括人口统计学、诊断和复发日期的详细信息、组织学、分期、国际预后指数、初始诊断和复发时的治疗及结果。应用卡方检验确定分类变量之间的统计学意义。生存曲线采用Kaplan–Meier方法生成。结果:我们的研究共纳入54例复发DLBCL患者,其中男性38例(70%),女性16例(30%)。约23例(43%)患者诊断时处于IV期,34例(63%)有B症状。诊断时最常见的R-IPI为II级,共24例(44%)患者。复发/难治性疾病再次活检时,只有6例(11%)未显示CD20表达,2例CD20阴性DLBCL患者对二线化疗有反应。复发/难治性DLBCL患者中,16例(29.6%)经挽救化疗后达到完全缓解。7例(13%)患者在二线治疗后接受自体骨髓移植巩固治疗。CD20阳性患者的中位总生存期为18个月,CD20阴性患者为13个月。结论:本研究表明,一小部分接受利妥昔单抗治疗的患者在复发时失去CD20表达。然而,尚不清楚这是否与较差的预后相关。