Department of Oncology and Surgical Sciences, Oncology Section, University of Padova,Padova, Italy.
Haematologica. 2012 Jan;97(1):56-63. doi: 10.3324/haematol.2011.049874. Epub 2011 Sep 20.
B-cell chronic lymphocytic leukemia is a clinically heterogeneous disease; some patients rapidly progress and die within a few years of diagnosis, whereas others have a long life expectancy with minimal or no treatment. Telomere length and telomerase levels have been proposed as prognostic factors; however, very few cases have been characterized for both parameters and no study has analyzed the prognostic value of the telomere/telomerase profile.
One hundred and seventy-three cases of chronic lymphocytic leukemia were characterized for telomere lengths and telomerase levels by real-time polymerase chain reaction. Data were correlated with established prognostic markers, IGVH mutational status and chromosomal aberrations, and clinical outcome.
Telomere lengths were inversely correlated with telomerase levels (r(s) = -0.213; P = 0.012), and most of the cases of chronic lymphocytic leukemia with high levels (above median) of telomerase had short (below median) telomeres (P = 0.0001). Telomerase levels were higher and telomeres were shorter in unmutated IGVH cases than in mutated IGVH ones (P<0.0001). Chronic lymphocytic leukemias with 11q, 17p deletion or 12 trisomy had significantly higher levels of telomerase and shorter telomeres than those with no chromosomal aberration or the sole 13q deletion (P < 0.001). Telomere length/telomerase level profiles identified subgroups of patients with different clinical outcomes (P < 0.0001), even within the subsets of chronic lymphocytic leukemia defined by IGVH mutational status or chromosomal aberrations. Short telomere/high telomerase profile was independently associated with more rapid disease progression.
Comprehensive analyses of telomeres, telomerase, chromosomal aberrations, and IGVH mutational status delineate groups of chronic lymphocytic leukemias with distinct biological characteristics and clinical outcomes. The telomere/telomerase profile may be particularly useful in refining the prognosis of chronic lymphocytic leukemia patients with mutated IGVH and no high-risk chromosomal aberrations.
B 细胞慢性淋巴细胞白血病是一种临床表现异质性疾病;一些患者在诊断后几年内迅速进展并死亡,而另一些患者则具有较长的预期寿命,无需或仅需最低限度的治疗。端粒长度和端粒酶水平已被提议作为预后因素;然而,只有极少数病例对这两个参数进行了特征描述,并且没有研究分析端粒/端粒酶谱的预后价值。
通过实时聚合酶链反应对 173 例慢性淋巴细胞白血病患者的端粒长度和端粒酶水平进行了特征描述。将数据与已建立的预后标志物、IGHV 突变状态和染色体异常以及临床结果进行了相关性分析。
端粒长度与端粒酶水平呈负相关(r(s)=-0.213;P=0.012),并且大多数端粒酶水平较高(高于中位数)的慢性淋巴细胞白血病患者的端粒较短(低于中位数)(P=0.0001)。未突变 IGHV 病例的端粒酶水平较高,端粒较短,而突变 IGHV 病例则较低(P<0.0001)。与无染色体异常或仅 13q 缺失相比,具有 11q、17p 缺失或 12 三体的慢性淋巴细胞白血病患者的端粒酶水平更高,端粒更短(P<0.001)。端粒长度/端粒酶水平谱可识别出具有不同临床结局的患者亚组(P<0.0001),即使在 IGHV 突变状态或染色体异常定义的慢性淋巴细胞白血病亚组内也是如此。短端粒/高端粒酶谱与疾病进展更快独立相关。
全面分析端粒、端粒酶、染色体异常和 IGHV 突变状态,可描绘出具有不同生物学特征和临床结局的慢性淋巴细胞白血病患者群体。端粒/端粒酶谱可能特别有助于细化 IGHV 突变且无高危染色体异常的慢性淋巴细胞白血病患者的预后。