Department of Thoracic Surgery, Henan Provincial People's Hospital (Zhengzhou University People's Hospital), Zhengzhou, China.
BMJ Open. 2017 Aug 21;7(8):e016913. doi: 10.1136/bmjopen-2017-016913.
To evaluate the prognostic relevance of four functional single nucleotide polymorphisms (SNPs) in (A>C, T>A, C>G, and C>T) on overall survival (OS) of non-small cell lung cancer (NSCLC) patients.
Retrospective cohort study.
Department of General Surgery, in a general hospital, Henan Province, China.
NSCLC patients aged ≥18 years, who were not receiving preoperative neoadjuvant therapies and had a blood sample available for genotyping, were eligible for inclusion. Those participants who were pregnant or breastfeeding, had a previous history of cancer, had other primary tumours, or who had had primary tumours of the skin and nasopharynx, were excluded from the study.
The primary endpoint was OS, which was calculated from the date of enrolment until the date of death or date of last follow-up.
There was a total of 1383 participants, with a median age of 63 years; 726 (52.5%) were male. Compared with the AA genotype, the variant AC/CC genotypes were independently associated with OS (HR 1.27, 95% CI 1.12 to 1.45 for AC genotype; HR 2.32, 95% CI 1.91 to 2.80 for CC genotype). Higher hazard ratios for associations between polymorphism and OS were observed in patients with adjuvant chemotherapy (HR 1.86, 95% CI 1.52 to 2.26) and radiotherapy for curative intent (HR 1.90, 95% CI 1.55 to 2.33).
The study confirmed the significant association between the SNP of CD133 and OS of NSCLC patients. Larger population-based studies in different ethnic groups are necessary to further validate the role and mechanisms of in NSCLC.
评估四个功能性单核苷酸多态性(SNPs)在非小细胞肺癌(NSCLC)患者总生存率(OS)中的预后相关性。
回顾性队列研究。
中国河南省某综合医院普外科。
符合以下条件的 NSCLC 患者有资格入组:年龄≥18 岁,未接受术前新辅助治疗,且有血样可供基因分型;排除孕妇或哺乳期妇女、有癌症病史、有其他原发性肿瘤、或有皮肤和鼻咽原发性肿瘤的患者。
主要终点是 OS,从入组日期计算到死亡日期或最后一次随访日期。
共纳入 1383 名患者,中位年龄为 63 岁,726 名(52.5%)为男性。与 AA 基因型相比,变异 AC/CC 基因型与 OS 独立相关(AC 基因型的 HR 为 1.27,95%CI 为 1.12 至 1.45;CC 基因型的 HR 为 2.32,95%CI 为 1.91 至 2.80)。对于接受辅助化疗(HR 1.86,95%CI 1.52 至 2.26)和根治性放疗(HR 1.90,95%CI 1.55 至 2.33)的患者,CD133 基因多态性与 OS 之间的关联具有更高的风险比。
本研究证实了 SNP 与 NSCLC 患者 OS 之间的显著相关性。需要在不同种族群体中进行更大规模的基于人群的研究,以进一步验证 SNP 在 NSCLC 中的作用和机制。