Zhong Xi, Zhou Yue, Cui Wanbin, Su Xin, Guo Zhexu, Hidasa Iko, Li Qincai, Wang Zhenning, Song Yongxi
Department of Surgical Oncology and General Surgery, Key Laboratory of Precision Diagnosis and Treatment of Gastrointestinal Tumors, Ministry of Education, The First Affiliated Hospital of China Medical University, Shenyang, China.
Department of Medical Oncology, The First Affiliated Hospital of China Medical University, Shenyang, China.
Front Pharmacol. 2020 May 15;11:706. doi: 10.3389/fphar.2020.00706. eCollection 2020.
Patients with locally advanced rectal cancer (LARC) are at higher risk of local and distant recurrence and are thus more vulnerable to metastatic diseases. Neoadjuvant chemoradiotherapy (nCRT) and subsequent curative resection with total mesorectal excision (TME) followed by adjuvant chemotherapy have been recommended by the National Comprehensive Cancer Network (NCCN) guidelines as standard of care for LARC patients. However, the efficacy of the addition of epidermal growth factor receptor (EGFR) inhibitors in kirsten rat sarcoma viral oncogene (KRAS)-wild type LARC patients remains uncertain.
PubMed, Embase, and Web of Science were searched to retrieve records on the application of EGFR inhibitors in a neoadjuvant setting for LARC patients. pCR was used as surrogate endpoint to perform data synthesis in a single-arm setting.
Ten cohorts covering 540 subjects were eligible in this systematic review. The pooled pCR rate for EGFR inhibitors was 15% (95% confidence interval (95% CI), 11-20%; I = 55.2%); the pooled estimates of Grade 3/4 diarrhea, Grade 3/4 hand-foot syndrome, Grade 3/4 acneiform rash were 17% (95% CI, 4-34%; I = 93.3%), 2% (95% CI, 0-5%; I = 13.7%), and 15% (95% CI, 9-22%; I = 65.4%), respectively.
The addition of EGFR inhibitors in the nCRT for KRAS-wild type LARC patients provides comparable efficacy and acceptable safety. However, the results should be interpreted cautiously due to the small amount of relevant data and need further confirmation by more future studies.
局部晚期直肠癌(LARC)患者发生局部和远处复发的风险较高,因此更容易发生转移性疾病。美国国立综合癌症网络(NCCN)指南推荐新辅助放化疗(nCRT),随后行全直肠系膜切除术(TME)根治性切除,然后进行辅助化疗,作为LARC患者的标准治疗方案。然而,在 Kirsten 大鼠肉瘤病毒癌基因(KRAS)野生型LARC患者中添加表皮生长因子受体(EGFR)抑制剂的疗效仍不确定。
检索了PubMed、Embase和Web of Science,以获取关于EGFR抑制剂在LARC患者新辅助治疗中应用的记录。将病理完全缓解(pCR)用作替代终点,在单臂研究中进行数据合成。
本系统评价纳入了10个队列,共540名受试者。EGFR抑制剂的汇总pCR率为15%(95%置信区间(95%CI),11%-20%;I² = 55.2%);3/4级腹泻、3/4级手足综合征、3/4级痤疮样皮疹的汇总估计发生率分别为17%(95%CI,4%-34%;I² = 93.3%)、2%(95%CI,0%-5%;I² = 13.7%)和15%(95%CI,9%-22%;I² = 65.4%)。
在KRAS野生型LARC患者的nCRT中添加EGFR抑制剂具有相当的疗效和可接受的安全性。然而,由于相关数据量较少,结果应谨慎解释,需要更多未来研究进一步证实。