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基质金属蛋白酶-2 多态性与中国一线铂类化疗治疗的非小细胞肺癌患者的临床结局。

Matrix metalloproteinase-2 polymorphisms and clinical outcome of Chinese patients with nonsmall cell lung cancer treated with first-line, platinum-based chemotherapy.

机构信息

State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, Institute of Genetics, School of Life Sciences, Fudan University, Shanghai, China.

出版信息

Cancer. 2012 Jul 15;118(14):3587-98. doi: 10.1002/cncr.26669. Epub 2011 Nov 9.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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)。

结果

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。

结论

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。

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