Fung Sarah S, Hillier Kortney L, Leger Chantal S, Sandhu Irwin, Vickars Linda M, Galbraith Paul F, Li Charles H, Leitch Heather A
Faculty of Medicine, University of British Columbia, BC, Canada.
Leuk Lymphoma. 2007 Jun;48(6):1087-91. doi: 10.1080/10428190701321277.
Monoclonal B-cell lymphocytosis (MBL) is a clonal lymphoproliferation with the immunophenotype of chronic lymphocytic leukemia (CLL) but a B-lymphocyte count of less than 5 x 10(9)/l and no lymphadenopathy, organomegaly, cytopenias or symptoms. We performed a retrospective analysis of patients with MBL (n = 46), Rai stage 0 CLL (n = 112) and Rai stage > or =1 CLL (n = 54). Median follow-up and range was 30 (0.1-120) months for MBL, 60 (0.1-309) months for stage 0 CLL and 54 (0.1-309) months for stage > or =1 CLL. None of the MBL patients required treatment compared with 24 of 112 (21%) stage 0 CLL and 28 of 54 (52%) stage > or =1 CLL patients (p < 0.0003). No MBL underwent aggressive transformation compared with 1 of 112 (0.8%) stage 0 CLL and 6 of 54 (11%) stage > or =1 CLL patients (p < 0.0003). Progression-free survival (PFS) appeared improved in MBL compared to stage 0 CLL, although this did not reach statistical significant (p = 0.07) due to the relatively short follow-up in the MBL group; two year PFS was 97.2% for MBL, 93.1% for stage 0 CLL, and 68% for stage > or =1 CLL patients (p < 0.0001 for stage > or =1 CLL compared with MBL and stage 0 CLL). This is the first study of outcome in MBL which demonstrates that patients have an improved disease course compared to stage 0 CLL patients. Over a median 2.5 years of follow-up, no MBL patients required treatment or died of CLL-related causes.
单克隆B淋巴细胞增多症(MBL)是一种具有慢性淋巴细胞白血病(CLL)免疫表型的克隆性淋巴细胞增殖,但B淋巴细胞计数低于5×10⁹/L,且无淋巴结病、器官肿大、血细胞减少或症状。我们对MBL患者(n = 46)、Rai 0期CLL患者(n = 112)和Rai≥1期CLL患者(n = 54)进行了回顾性分析。MBL的中位随访时间及范围为30(0.1 - 120)个月,0期CLL为60(0.1 - 309)个月,≥1期CLL为54(0.1 - 309)个月。与112例0期CLL患者中的24例(21%)以及54例≥1期CLL患者中的28例(52%)相比,没有MBL患者需要治疗(p < 0.0003)。与112例0期CLL患者中的1例(0.8%)以及54例≥1期CLL患者中的6例(11%)相比,没有MBL患者发生侵袭性转化(p < 0.0003)。与0期CLL相比,MBL的无进展生存期(PFS)似乎有所改善,不过由于MBL组随访时间相对较短,这未达到统计学显著性(p = 0.07);MBL患者的两年PFS为97.2%,0期CLL为93.1%,≥1期CLL为68%(≥1期CLL与MBL及0期CLL相比,p < 0.0001)。这是第一项关于MBL预后的研究,表明与0期CLL患者相比,MBL患者的病程有所改善。在中位2.5年的随访期间,没有MBL患者需要治疗或死于CLL相关原因。