Mei Z B, Duan C Y, Li C B, Cui L, Ogino S
Department of Anorectal Surgery, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai
State Key Laboratory of Trauma, Burns and Combined Injury, Second Department of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing.
Ann Oncol. 2016 Oct;27(10):1836-48. doi: 10.1093/annonc/mdw264. Epub 2016 Jul 19.
Somatic mutations in the phosphatidylinositol-4,5-bisphosphate 3-kinase/AKT pathway play a vital role in carcinogenesis. Approximately 15%-20% of colorectal cancers (CRCs) harbor activating mutations in PIK3CA, making it one of the most frequently mutated genes in CRC. We thus carried out a systematic review and meta-analysis investigating the prognostic significance of PIK3CA mutations in CRC.
Electronic databases were searched from inception through May 2015. We extracted the study characteristics and prognostic data of each eligible study. The hazard ratio (HR) and 95% confidence interval (CI) were derived and pooled using the random-effects Mantel-Haenszel model.
Twenty-eight studies enrolling 12 747 patients were eligible for inclusion. Data on overall survival (OS) and progression-free survival (PFS) were available from 19 and 10 studies, respectively. Comparing PIK3CA-mutated CRC patients with PIK3CA-wild-type CRC patients, the summary HRs for OS and PFS were 0.96 (95% CI 0.83-1.12) and 1.20 (95% CI 0.98-1.46), respectively. The trim-and-fill, Copas model and subgroup analyses stratified by the study characteristics confirmed the robustness of the results. Five studies reported the CRC prognosis for PIK3CA mutations in exons 9 and 20 separately; neither exon 9 mutation nor exon 20 mutation in PIK3CA was significantly associated with patient survival.
Our findings suggest that PIK3CA mutation has the neutral prognostic effects on CRC OS and PFS. Evidence was accumulating for the establishment of CRC survival between PIK3CA mutations and patient-specific clinical or molecular profiles.
磷脂酰肌醇-4,5-二磷酸3-激酶/AKT通路中的体细胞突变在致癌过程中起着至关重要的作用。大约15%-20%的结直肠癌(CRC)存在PIK3CA激活突变,使其成为CRC中最常发生突变的基因之一。因此,我们进行了一项系统评价和荟萃分析,以研究PIK3CA突变在CRC中的预后意义。
从数据库建立至2015年5月进行电子数据库检索。我们提取了每项符合条件研究的研究特征和预后数据。使用随机效应Mantel-Haenszel模型得出并汇总风险比(HR)和95%置信区间(CI)。
28项纳入12747例患者的研究符合纳入标准。分别有19项和10项研究提供了总生存期(OS)和无进展生存期(PFS)的数据。将PIK3CA突变的CRC患者与PIK3CA野生型CRC患者进行比较,OS和PFS的汇总HR分别为0.96(95%CI 0.83-1.12)和1.20(95%CI 0.98-1.46)。通过修剪填充法、Copas模型以及根据研究特征进行的亚组分析证实了结果的稳健性。五项研究分别报告了外显子9和20中PIK3CA突变的CRC预后;PIK3CA外显子9突变和外显子20突变均与患者生存无显著相关性。
我们的研究结果表明,PIK3CA突变对CRC的OS和PFS具有中性预后影响。关于PIK3CA突变与患者特异性临床或分子特征之间建立CRC生存关系的证据正在积累。