Solomon B M, Chaffee K G, Moreira J, Schwager S M, Cerhan J R, Call T G, Kay N E, Slager S L, Shanafelt T D
University of South Dakota Sanford School of Medicine, Vermillion, SD, USA.
Avera Medical Group Oncology and Hematology, Sioux, SD, USA.
Leukemia. 2016 Feb;30(2):331-6. doi: 10.1038/leu.2015.235. Epub 2015 Aug 27.
It is unknown whether individuals with monoclonal B-cell lymphocytosis (MBL) are at risk for adverse outcomes associated with chronic lymphocytic leukemia (CLL), such as the risk of non-hematologic cancer. We identified all locally residing individuals diagnosed with high-count MBL at Mayo Clinic between 1999 and 2009 and compared their rates of non-hematologic cancer with that of patients with CLL and two control cohorts: general medicine patients and patients who underwent clinical evaluation with flow cytometry but who had no hematologic malignancy. After excluding individuals with prior cancers, there were 107 high-count MBL cases, 132 CLL cases, 589 clinic controls and 482 flow cytometry controls. With 4.6 years median follow-up, 14 (13%) individuals with high-count MBL, 21 (4%) clinic controls (comparison MBL P<0.0001), 18 (4%) flow controls (comparison MBL P=0.0001) and 16 (12%) CLL patients (comparison MBL P=0.82) developed non-hematologic cancer. On multivariable Cox regression analysis, individuals with high-count MBL had higher risk of non-hematologic cancer compared with flow controls (hazard ratio (HR)=2.36; P=0.04) and borderline higher risk compared with clinic controls (HR=2.00; P=0.07). Patients with high-count MBL appear to be at increased risk for non-hematologic cancer, further reinforcing that high-count MBL has a distinct clinical phenotype despite low risk of progression to CLL.
尚不清楚单克隆B细胞淋巴细胞增多症(MBL)患者是否存在与慢性淋巴细胞白血病(CLL)相关的不良结局风险,例如非血液系统癌症风险。我们识别出1999年至2009年间在梅奥诊所诊断为高计数MBL的所有本地居民,并将他们的非血液系统癌症发生率与CLL患者以及两个对照队列进行比较:普通内科患者和接受流式细胞术临床评估但无血液系统恶性肿瘤的患者。排除既往有癌症的个体后,有107例高计数MBL病例、132例CLL病例、589例临床对照和482例流式细胞术对照。中位随访4.6年,14例(13%)高计数MBL个体、21例(4%)临床对照(与MBL比较P<0.0001)、18例(4%)流式对照(与MBL比较P=0.0001)和16例(12%)CLL患者(与MBL比较P=0.82)发生了非血液系统癌症。在多变量Cox回归分析中,高计数MBL个体与流式对照相比,发生非血液系统癌症的风险更高(风险比[HR]=2.36;P=0.04),与临床对照相比风险略高(HR=2.00;P=0.07)。高计数MBL患者发生非血液系统癌症的风险似乎增加,进一步证实高计数MBL尽管进展为CLL的风险较低,但具有独特的临床表型。