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.
Background:
Human epidermal growth factor receptor 2 (HER2) amplification is a molecular driver for a subset of colorectal cancers (CRCs) and one of the major causes of anti-epidermal growth factor receptor (EGFR) treatment failure. Compared to dual anti-HER2 treatments, which have been shown to be effective in HER2-positive metastatic CRC patients, single-agent anti-HER2 therapy is rarely used to treat CRC.
Case Summary:
Herein, we report a case of RAS/BRAF-wild-type metastatic CRC that was identified as HER2-positive through circulating tumor DNA (ctDNA) testing by next-generation sequencing following the failure of two lines of therapy. Subsequently, the patient was given lapatinib monotherapy that led to a partial response with a progression-free survival of 7.9 mo. Moreover, serial ctDNA detection was used to monitor the efficacy of lapatinib. The aberration of HER2 copy number disappeared when radiographic assessment revealed a partial response. However, a high level of HER2 amplification was detected again at the time of disease progression. Finally, a phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha mutation was identified at the time of tumor progression, which may explain the acquired resistance to lapatinib.
Conclusion:
This is the first case report of HER2-positive RAS/BRAF wild-type metastatic CRC patient responding to lapatinib monotherapy. It highlights that ctDNA testing is an effective and feasible approach to evaluate the efficacy of anti-HER2 therapy.
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.
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