Epidemiology, University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA.
Leuk Lymphoma. 2010 Apr;51(4):598-605. doi: 10.3109/10428190903582804.
In acute myeloid leukemia (AML), cytogenetics predicts treatment outcome for the favorable and poor subgroups but not for the intermediate subgroup. Polymorphisms within the nucleotide excision repair (NER) pathway may lead to interindividual differences in DNA repair capacity, influencing outcome. We studied the role of six polymorphisms (ERCC1 Gln504Lys, XPD Lys751Gln, XPC Ala499Val, XPC Lys939Gln, XPG Asp1104His, and CCNH Val270Ala) in overall and disease-free survival among 170 adult de novo patients with intermediate cytogenetics (diploid [n = 117]; non-diploid [n = 53]), treated with induction chemotherapy. Kaplan-Meier and Cox proportional hazards models were performed. Diploid patients with the XPD AC/CC genotype survived shorter than those with the wild-type genotype (median survival 22 vs. 40 months, p = 0.03). Diploid patients with XPC CT/TT genotype survived shorter than those with the wild-type genotype (median survival 15 vs. 30 months, p = 0.02). After adjusting for clinical and sociodemographic variables, patients carrying both XPD AC/CC and XPC CT/TT had a greater than two-fold increased risk of dying, compared to those with the wild-type genotypes (HR = 2.49; 95% CI: 1.06-5.85). No associations were observed for disease-free survival. This combined genotype may modulate treatment effect, decreasing overall survival. These findings could in the future help select treatments for patients with normal cytogenetics.
在急性髓系白血病(AML)中,细胞遗传学可预测有利和不良亚组的治疗结果,但不能预测中间亚组的结果。核苷酸切除修复(NER)途径中的多态性可能导致个体间 DNA 修复能力的差异,从而影响结果。我们研究了六个多态性(ERCC1 Gln504Lys、XPD Lys751Gln、XPC Ala499Val、XPC Lys939Gln、XPG Asp1104His 和 CCNH Val270Ala)在 170 名中间细胞遗传学(二倍体 [n = 117];非二倍体 [n = 53])的成年初治 AML 患者的总生存和无病生存中的作用,这些患者接受诱导化疗。进行了 Kaplan-Meier 和 Cox 比例风险模型分析。XPD AC/CC 基因型的二倍体患者的生存时间短于野生型基因型(中位生存时间 22 与 40 个月,p = 0.03)。XPC CT/TT 基因型的二倍体患者的生存时间短于野生型基因型(中位生存时间 15 与 30 个月,p = 0.02)。在校正了临床和社会人口统计学变量后,与野生型基因型相比,携带 XPD AC/CC 和 XPC CT/TT 的患者死亡风险增加了两倍以上(HR = 2.49;95%CI:1.06-5.85)。无病生存无相关性。这种联合基因型可能调节治疗效果,降低总生存。这些发现将来可能有助于为正常细胞遗传学的患者选择治疗方法。