U.O.C. di Ematologia, Azienda Ospedaliera di Cosenza, Italy.
Am J Hematol. 2013 Jul;88(7):539-44. doi: 10.1002/ajh.23448. Epub 2013 Jun 12.
Total body computed tomography (TB-CT) scan is not mandatory in the diagnostic/staging algorithm of chronic lymphocytic leukemia (CLL). The aim of this study was to determine the value and prognostic significance of TB-CT scan in early stage CLL patients. Baseline TB-CT scan was performed in 240 Binet stage A CLL patients (179 Rai low- and 61 Rai intermediate-risk) included in a prospective multicenter observational study (clinicaltrial.gov ID:NCT00917549). The cohort included 69 clinical monoclonal B lymphocytosis (cMBLs). Patients were restaged considering only radiological data. Following TB-CT scans, 20% of cases reclassified as radiologic Binet (r-Binet) stage B. r-Binet B patients showed a higher incidence of unfavorable cytogenetic abnormalities (P = 0.027), as well as a shorter PFS (P = 0.001). At multivariate analysis, r-Binet stage [HR = 2.48; P = 0.004] and IGHV mutational status [HR = 3.01; P = 0.002] retained an independent predictive value for PFS. Among 179 Rai low-risk cases, 100 were redefined as r-Rai intermediate-risk based upon TB-CT scan data, showing a higher rate of cases with higher ZAP-70 (P = 0.033) and CD38 expression (P = 0.029) and β2-microglobulin levels (P < 0.0001), as well as a shorter PFS than those with r-Rai low-risk (P = 0.008). r-Rai stage [HR = 2.78; P = 0.046] and IGHV mutational status [HR = 4.25; P = 0.009] retained a significant predictive value for PFS at multivariate analysis. Forty-two percent of cMBL patients were reclassified as r-small lymphocytic lymphomas (r-SLLs) by TB-CT scan. TB-CT scan appears to provide relevant information in early stage CLL related to the potential and the timing of patients to progress towards the more advanced disease stages.
全身计算机断层扫描(TB-CT)并非慢性淋巴细胞白血病(CLL)诊断/分期算法中的强制性检查。本研究旨在确定 TB-CT 扫描在早期 CLL 患者中的价值和预后意义。在一项前瞻性多中心观察性研究(clinicaltrial.gov ID:NCT00917549)中,对 240 名 Binet 分期 A 的 CLL 患者(179 名 Rai 低危和 61 名 Rai 中危)进行了基线 TB-CT 扫描。该队列包括 69 例临床单克隆 B 淋巴细胞增多症(cMBL)。仅根据影像学数据重新分期患者。进行 TB-CT 扫描后,20%的病例重新分类为影像学 Binet(r-Binet)分期 B。r-Binet B 患者具有更高的不良细胞遗传学异常发生率(P=0.027),以及更短的无进展生存期(P=0.001)。多变量分析显示,r-Binet 分期[HR=2.48;P=0.004]和 IGHV 突变状态[HR=3.01;P=0.002]对 PFS 具有独立的预测价值。在 179 例 Rai 低危病例中,根据 TB-CT 扫描数据,有 100 例重新定义为 r-Rai 中危,这些病例具有更高的 ZAP-70(P=0.033)和 CD38 表达(P=0.029)和β2-微球蛋白水平(P<0.0001),以及更短的无进展生存期,与 r-Rai 低危相比(P=0.008)。r-Rai 分期[HR=2.78;P=0.046]和 IGHV 突变状态[HR=4.25;P=0.009]在多变量分析中对 PFS 具有显著的预测价值。42%的 cMBL 患者经 TB-CT 扫描重新分类为 r-小淋巴细胞淋巴瘤(r-SLL)。TB-CT 扫描似乎为早期 CLL 提供了与患者向更晚期疾病阶段进展的潜力和时机相关的重要信息。