Response of human epidermal growth factor receptor 2-positive colorectal cancer to lapatinib monotherapy: A case

Ji-Lin Guan1, Jian-Hua Liu1, Qing Wang2

  • 1Department of Oncology, Guangdong Provincial People's Hospital and Guangdong Academy of Medical Sciences, Guangzhou 510655, Guangdong Province, China.

Abstract

Insights

This case report shows lapatinib monotherapy can be effective for HER2-positive metastatic colorectal cancer (CRC) lacking RAS/BRAF mutations. Circulating tumor DNA (ctDNA) monitoring effectively tracked treatment response and resistance.

Area of Science:

  • Oncology
  • Molecular Diagnostics
  • Cancer Therapeutics

Background:

  • HER2 amplification drives a subset of colorectal cancers (CRCs) and causes anti-EGFR treatment resistance.
  • Single-agent anti-HER2 therapy is underutilized in CRC compared to dual-agent approaches.
  • HER2-positive metastatic CRC requires novel therapeutic strategies.

Observation:

  • A patient with RAS/BRAF-wild-type metastatic CRC, identified as HER2-positive via ctDNA testing, received lapatinib monotherapy post-failure of two prior therapies.
  • Lapatinib monotherapy resulted in a partial response and 7.9 months of progression-free survival.
  • Serial ctDNA analysis revealed dynamic changes in HER2 amplification, correlating with treatment response and subsequent progression.

Findings:

  • This is the first reported case of a HER2-positive, RAS/BRAF wild-type metastatic CRC patient responding to lapatinib monotherapy.
  • ctDNA testing proved effective for monitoring lapatinib efficacy in this patient.
  • Acquired resistance to lapatinib was associated with the emergence of a PIK3CA mutation.

Implications:

  • Lapatinib monotherapy represents a potential treatment option for select HER2-positive metastatic CRC patients.
  • ctDNA monitoring offers a feasible method for evaluating anti-HER2 therapy efficacy in CRC.
  • Understanding resistance mechanisms, such as PIK3CA mutations, is crucial for optimizing CRC treatment strategies.