Chemotherapy plus panitumumab/cetuximab versus chemotherapy plus bevacizumab in wild-type KRAS/RAS metastatic colorectal cancer: a meta-analysis

Expert Rev Anticancer Ther. 2022 Dec;22(12):1333-1347. doi: 10.1080/14737140.2022.2147512. Epub 2022 Nov 22.

Abstract

Objective: It remains controversial which targeted monoclonal antibodies combined with chemotherapy can provide better efficacy in wild-type KRAS/RAS metastatic colorectal cancer (mCRC) patients. Therefore, we used this meta-analysis to assess the latest evidence of clinical outcomes.

Materials and methods: We systematically searched PubMed, Web of Science, Cochrane Library and Embase databases for eligible studies published from database inception to May 2022. RevMan 5.4 was used to conduct the meta-analysis.

Results: 11 RCTs involving a total of 3575 patients were included. Meta-analysis showed that EGFR inhibitors significantly prolonged the overall survival (OS) [HR = 0.83, 95%CI (0.73, 0.94), P = 0.003] and overall response rate (ORR) [RR = 1.11, 95%CI (1.05, 1.18), P = 0.0003] compared to VEGF inhibitors in wild-type KRAS/RAS mCRC patients, but no significant difference in progression-free survival (PFS) [HR = 0.96, 95%CI (0.87, 1.07), P = 0.50]. In subgroup analysis, the survival benefit of EGFR inhibitors was limited to first-line treatment.

Conclusion: Our study showed that EGFR inhibitors were superior to VEGF inhibitors in wild-type KRAS/RAS mCRC patients, especially in patients with first-line treatment. However, subsequent large sample, multi-center RCTs are needed to further verify our conclusions.

Keywords: Metastatic colorectal cancer; bevacizumab; cetuximab; chemotherapy; meta analysis; panitumumab.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bevacizumab / pharmacology
  • Cetuximab / pharmacology
  • Colorectal Neoplasms* / drug therapy
  • Colorectal Neoplasms* / genetics
  • Humans
  • Panitumumab
  • Proto-Oncogene Proteins p21(ras) / genetics
  • Vascular Endothelial Growth Factor A*

Substances

  • Bevacizumab
  • Cetuximab
  • KRAS protein, human
  • Panitumumab
  • Proto-Oncogene Proteins p21(ras)
  • Vascular Endothelial Growth Factor A