Cancer Center, The First Hospital of Jilin University, 71 Xinmin Ave, Changchun, China.
Department of Radiation Oncology, The First Hospital of Jilin University, 71 Xinmin Ave, Changchun, China.
Crit Rev Oncol Hematol. 2018 Apr;124:11-20. doi: 10.1016/j.critrevonc.2018.02.006. Epub 2018 Feb 7.
We conducted a systematic review and meta-analysis to investigate the impact of p16(INK4a) status on survival benefits in head and neck squamous cell cancer (HNSCC) after anti-epidermal growth factor receptor (EGFR) based treatments.
We identified studies assessing anti-EGFR based versus non-anti-EGFR based regimens in patients with unresectable locoregionally advanced, recurrent or metastatic HNSCC. The primary endpoint was progression-free survival (PFS). We assessed the risk of bias in each included study. Random-effects models were used to estimate the efficacy of anti-EGFR based treatments for the p16-positive/p16-negative patients and prespecified subgroups defined by treatment modalities (chemotherapy or radiotherapy).
Ten studies with 1929 patients were included. Adding an EGFR inhibitor did not significantly improve PFS or overall survival (OS) in either p16-negative or p16-positive disease. Subgroup analyses suggested a significant PFS benefit (hazard ratio [HR] 0.58; P < 0.001) of adding an EGFR inhibitor to chemotherapy versus chemotherapy for p16-negative disease. The p16-negativity was also associated with a significant OS benefit (HR 0.77; P = 0.003) when studies with high risk of bias were excluded. In contrast, adding an EGFR inhibitor to chemotherapy provided no benefit in either PFS or OS for p16-positive disease. No benefit was shown in either PFS or OS from adding an EGFR inhibitor to radiotherapy or chemoradiotherapy versus chemoradiotherapy regardless of p16 status.
For the first time, our meta-analysis provides evidence that efficacy of anti-EGFR based treatments could be dependent on both p16 status and treatment modality. p16 status is likely to have a role in predicting survival to anti-EGFR based treatments in recurrent or metastatic HNSCC.
我们进行了一项系统评价和荟萃分析,以研究 p16(INK4a)状态对头颈部鳞状细胞癌(HNSCC)患者接受抗表皮生长因子受体(EGFR)治疗后的生存获益的影响。
我们确定了评估抗 EGFR 治疗与非抗 EGFR 治疗在不可切除的局部晚期、复发性或转移性 HNSCC 患者中的研究。主要终点是无进展生存期(PFS)。我们评估了每个纳入研究的偏倚风险。使用随机效应模型来估计抗 EGFR 治疗对 p16 阳性/阴性患者以及根据治疗方式(化疗或放疗)定义的预设亚组的疗效。
纳入了 10 项研究,共 1929 例患者。添加 EGFR 抑制剂并未显著改善 p16 阴性或阳性疾病的 PFS 或总生存期(OS)。亚组分析表明,与化疗相比,在 p16 阴性疾病中添加 EGFR 抑制剂可显著改善 PFS(风险比 [HR] 0.58;P<0.001)。当排除高偏倚风险的研究时,p16 阴性也与显著的 OS 获益相关(HR 0.77;P=0.003)。相反,对于 p16 阳性疾病,添加 EGFR 抑制剂对 PFS 或 OS 均无获益。无论 p16 状态如何,添加 EGFR 抑制剂对放疗或放化疗与放化疗相比,在 PFS 或 OS 方面均未显示获益。
我们的荟萃分析首次提供了证据,表明抗 EGFR 治疗的疗效可能取决于 p16 状态和治疗方式。p16 状态可能在预测复发性或转移性 HNSCC 患者对基于 EGFR 的治疗的生存获益方面具有作用。