State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, Institute of Genetics, School of Life Sciences, Fudan University, Shanghai, China.
Cancer. 2012 Jul 15;118(14):3587-98. doi: 10.1002/cncr.26669. Epub 2011 Nov 9.
Matrix metalloproteinase-2 (MMP-2) is well known for its critical role in cell survival and cancer development. It also plays an important role in hematopoietic recovery after chemotherapy-induced myelosuppression. In this study, the authors investigated the association of MMP-2 polymorphisms with treatment efficacy and the occurrence of severe toxicity in patients with nonsmall cell lung cancer (NSCLC) who were receiving first-line, platinum-based chemotherapy.
A pharmacogenetic association study was performed in 663 Chinese patients who had inoperable stage III/IV NSCLC and were receiving first-line, platinum-based regimens. Information about objective response, progression-free survival, overall survival, grade 3 or 4 gastrointestinal toxicity (nausea/vomiting), and hematologic toxicity (neutropenia, anemia, thrombocytopenia) was available. Sixteen tag single nucleotide polymorphisms (SNPs) of MMP-2 were assessed.
In 7 polymorphisms, significant associations were observed with the incidence of grade 3 or 4 neutropenia. The variant homozygotes of reference SNP rs12934241 exhibited the most significant effect on the risk of neutropenia, leading to an incidence rate that increased from 12.3% (for the C/C genotype) to 50% (for the T/T genotype; odds ratio, 8.33; P = 8.8 × 10(-5)). Stratified analyses indicated that rs12934241 exhibited a much stronger influence in the cisplatin-gemcitabine regimen subgroup than subgroups that received other regimens (P(interaction) = .003). Further haplotype analyses produced results that were consistent with results from single-SNP analyses. However, no significant association was observed between MMP-2 polymorphisms and treatment efficacy, including response rate, clinical benefit, progression-free survival, and overall survival.
To the authors' knowledge, this study provides the first evidence for a predictive role of MMP-2 polymorphisms in the variability of severe chemotherapy-related neutropenia among Chinese patients with platinum-treated, advanced NSCLC.
基质金属蛋白酶-2(MMP-2)因其在细胞存活和癌症发展中的关键作用而广为人知。它在化疗引起的骨髓抑制后造血恢复中也起着重要作用。在这项研究中,作者研究了 MMP-2 多态性与接受一线铂类化疗的非小细胞肺癌(NSCLC)患者治疗效果和严重毒性发生的相关性。
对 663 例无法手术的 III/IV 期 NSCLC 接受一线铂类方案的中国患者进行了一项药物遗传学相关性研究。可获得客观缓解、无进展生存期、总生存期、3 或 4 级胃肠道毒性(恶心/呕吐)和血液学毒性(中性粒细胞减少症、贫血、血小板减少症)的信息。评估了 MMP-2 的 16 个标签单核苷酸多态性(SNP)。
在 7 个多态性中,观察到与 3 或 4 级中性粒细胞减少症的发生率存在显著相关性。参考 SNP rs12934241 的变异纯合子对中性粒细胞减少症的风险影响最大,导致中性粒细胞减少症的发生率从 12.3%(C/C 基因型)增加到 50%(T/T 基因型;优势比,8.33;P = 8.8×10(-5))。分层分析表明,rs12934241 在顺铂-吉西他滨方案亚组中的影响比接受其他方案的亚组强得多(P(交互) =.003)。进一步的单体型分析产生的结果与单 SNP 分析的结果一致。然而,MMP-2 多态性与治疗效果(包括缓解率、临床获益、无进展生存期和总生存期)之间没有显著相关性。
据作者所知,这项研究首次提供了证据,证明 MMP-2 多态性在中国接受铂类治疗的晚期 NSCLC 患者中与严重化疗相关中性粒细胞减少症的变异性具有预测作用。