Petrelli F, Pezzica E, Cabiddu M, Coinu A, Borgonovo K, Ghilardi M, Lonati V, Corti D, Barni S
Department of Oncology, Division of Medical Oncology, Azienda Ospedaliera Treviglio, Treviglio, BG, Italy,
J Gastrointest Cancer. 2015 Sep;46(3):212-8. doi: 10.1007/s12029-015-9716-1.
Tumour budding is defined as the presence of isolated or small clusters of malignant cells at the invasive edge of the tumour. It is considered a negative prognostic factor in colorectal cancer (CRC) and is associated with a poor outcome and adverse pathological features. Here, we report a meta-analysis of the association of tumour budding and survival in stage II CRC patients.
PubMed, EMBASE, Web of Science and SCOPUS were searched for studies that assessed the relationship between tumour budding and 5-year overall survival (OS) in stage II CRC patients. Published data were extracted and used to compute odds ratios (ORs) for death at 5 years and hazard ratios (HRs) for survival amongst patients with respect to the extent of tumour budding, using multivariate analysis. Data were pooled using the Mantel-Haenszel random effect model.
We analysed 12 studies that included a total of 1652 patients. High-grade budding was associated with worse OS at 5 years (OR for death, 6.25; 95 % confidence interval [CI], 4.04-9.67; P < 0.00001). The absolute difference in 5-year OS was -25 % (95 % CI, -18- - 33 %, P < 0.00001). It was particularly noteworthy that the presence of high-grade budding was associated with an increased risk of death (HR for death, 3.68; 95 % CI, 2.16-6.28, P < 0.00001).
Tumour budding is associated with worse survival in stage II CRC, in particular in pT3N0M0 patients. It could therefore potentially be used when deciding whether to administer adjuvant chemotherapy in high-risk node negative CRC patients.
肿瘤芽生被定义为肿瘤浸润边缘存在孤立的或小簇状的恶性细胞。它被认为是结直肠癌(CRC)的一个不良预后因素,与预后不良及不良病理特征相关。在此,我们报告一项关于II期CRC患者中肿瘤芽生与生存关系的荟萃分析。
检索PubMed、EMBASE、Web of Science和SCOPUS,查找评估II期CRC患者肿瘤芽生与5年总生存(OS)关系的研究。提取已发表的数据,并使用多变量分析计算不同肿瘤芽生程度患者的5年死亡比值比(OR)和生存风险比(HR)。采用Mantel-Haenszel随机效应模型汇总数据。
我们分析了12项研究,共纳入1652例患者。高级别芽生与5年时较差的OS相关(死亡OR为6.25;95%置信区间[CI]为4.04 - 9.67;P < 0.00001)。5年OS的绝对差异为 - 25%(95% CI为 - 18 - - 33%,P < 0.00001)。特别值得注意的是,高级别芽生的存在与死亡风险增加相关(死亡HR为3.68;95% CI为2.16 - 6.28,P < 0.00001)。
肿瘤芽生与II期CRC患者较差的生存相关,尤其是pT3N0M0患者。因此,在决定是否对高危淋巴结阴性CRC患者进行辅助化疗时,它可能具有潜在用途。