Gentile Massimo, Mauro Francesca Romana, Calabrese Elisabetta, De Propris Maria Stefania, Giammartini Elena, Mancini Francesca, Milani Maria Laura, Guarini Anna, Foà Robin
Division of Haematology, Dipartimento di Biotecnologie Cellulari ed Ematologia, University La Sapienza, Rome, Italy.
Br J Haematol. 2005 Aug;130(4):549-57. doi: 10.1111/j.1365-2141.2005.05659.x.
The purpose of this study was to assess in chronic lymphocytic leukaemia (CLL) patients the prevalence and clinical impact of CD38 expression, evaluated prospectively at disease presentation, and to verify whether this parameter changes over time. In 242 consecutive and untreated CLL patients, the percentage of CD38+ cases, according to the 7%, 20% and 30% cut-off points, was 21%, 17% and 14%, respectively. Using the 7% threshold, CD38 positivity correlated with male sex, intermediate and high-risk (Rai I-IV) disease, lower Hb and platelet levels, and higher lymphocyte count. Furthermore, patients with a CD38 expression>or=7% showed a significantly lower 3-year probability of treatment-free survival (TFS) than CD38- patients (P<0.0001). At multivariate analysis, CD38 expression remained significantly associated to TFS, together with stage, lymphocyte count and morphology. Also, in the 146 patients with stage 0 CLL a CD38 expression>or=7% identified a subgroup of patients with a significantly lower 3-year probability of TFS (P=0.0005). Furthermore, this parameter did not change in 30 of 31 (97%) re-evaluated patients. In conclusion, this study indicates that, when tested at diagnosis and on fresh material, a CD38 expression>or=7% is an important parameter for the identification of early CLL patients with more aggressive disease and that its expression remains stable over time.
本研究旨在评估慢性淋巴细胞白血病(CLL)患者中CD38表达的患病率及其临床影响,这些评估在疾病初发时进行前瞻性研究,并验证该参数是否随时间变化。在242例未经治疗的连续性CLL患者中,根据7%、20%和30%的截断点,CD38阳性病例的百分比分别为21%、17%和14%。采用7%的阈值时,CD38阳性与男性、中高危(Rai I-IV期)疾病、较低的血红蛋白和血小板水平以及较高的淋巴细胞计数相关。此外,CD38表达≥7%的患者无治疗生存期(TFS)的3年概率显著低于CD38阴性患者(P<0.0001)。多因素分析显示,CD38表达与TFS仍显著相关,同时与分期、淋巴细胞计数和形态学相关。此外,在146例0期CLL患者中,CD38表达≥7%的患者亚组的TFS 3年概率显著较低(P=0.0005)。此外,在31例重新评估的患者中有30例(97%)该参数未发生变化。总之,本研究表明,在诊断时对新鲜样本进行检测时,CD38表达≥7%是识别具有更侵袭性疾病的早期CLL患者的重要参数,且其表达随时间保持稳定。