Department of Internal Medicine, University of California, Riverside, CA 92521, USA.
School of Medicine, King Edward Medical University/Mayo Hospital, Lahore 54000, Pakistan.
Curr Oncol. 2023 Sep 7;30(9):8266-8277. doi: 10.3390/curroncol30090600.
Recent trials provide evidence that HER2 is a potential new target for patients with colorectal cancer. While HER2-positive tumors do not show a very encouraging response to anti-HER2-positive agents like trastuzumab alone, promising results have been observed when combined with other synergistically acting tyrosine kinase inhibitors (TKIs). Our meta-analysis was conducted following the Cochrane Handbook and written following the PRISMA guidelines. The protocol was registered on PROSPERO with the registration number CRD42022338935. After a comprehensive search for relevant articles, 14 CTs were identified and uploaded to Rayyan, and six trials were ultimately selected for inclusion. The meta-analysis revealed that a median of three prior lines of therapy was used before enrolling in the six trials comprising 238 patients with HER2-positive metastatic colorectal cancer (mCRC). The pooled objective response rate (ORR) and disease control rate (DCR) were 31.33% (95% confidence interval [CI] 24.27-38.39) and 74.37% (95% CI 64.57-84.17), respectively. The pooled weighted progression-free survival (PFS) was 6.2 months. The pooled ORR and DCR meta-analysis indicate a significant response to HER2-targeted therapy in this patient in HER2-positive mCRC. Additionally, a pooled PFS of 6.2 months suggests that HER2-targeted treatment regimens are associated with a meaningful improvement in survival outcomes in this population.
最近的临床试验提供了证据,表明 HER2 是结直肠癌患者的一个潜在新靶点。虽然 HER2 阳性肿瘤对曲妥珠单抗等抗 HER2 阳性药物的单独治疗反应并不十分令人鼓舞,但当与其他协同作用的酪氨酸激酶抑制剂 (TKI) 联合使用时,已经观察到了有希望的结果。我们的荟萃分析遵循 Cochrane 手册进行,并按照 PRISMA 指南进行编写。该方案已在 PROSPERO 上注册,注册号为 CRD42022338935。在全面搜索相关文章后,确定了 14 项 CT,并将其上传至 Rayyan,最终选择了 6 项试验进行纳入。荟萃分析显示,纳入的 6 项包含 238 例 HER2 阳性转移性结直肠癌 (mCRC) 患者的试验中,中位数有 3 线治疗前药物。汇总的客观缓解率 (ORR) 和疾病控制率 (DCR) 分别为 31.33%(95%置信区间 [CI] 24.27-38.39)和 74.37%(95% CI 64.57-84.17)。汇总的加权无进展生存期 (PFS) 为 6.2 个月。汇总的 ORR 和 DCR 荟萃分析表明,在 HER2 阳性 mCRC 患者中,HER2 靶向治疗具有显著的反应。此外,6.2 个月的汇总 PFS 表明,HER2 靶向治疗方案与该人群的生存结果显著改善相关。