Case Report: Dramatic response to amivantamab plus chemotherapy in EGFR G719A–mutant lung adenocarcinoma with liver and peritoneal metastases - Report - MDSpire
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Case Report: Dramatic response to amivantamab plus chemotherapy in EGFR G719A–mutant lung adenocarcinoma with liver and peritoneal metastases
Clinical Report: Significant Response to Amivantamab Combined with Chemotherapy
Overview
This case study presents a 52-year-old male with stage IVB lung adenocarcinoma and an uncommon EGFR G719A mutation who achieved a near-complete response to amivantamab combined with chemotherapy after multiple prior treatments. The response was durable for over nine months, highlighting the potential of this combination therapy in high-risk patients.
Background
Epidermal growth factor receptor (EGFR) mutations are common in non-small cell lung cancer (NSCLC), but uncommon mutations like G719A present unique challenges in treatment. Patients with hepatic metastases and uncommon mutations often have limited therapeutic options and poor prognoses. The efficacy of amivantamab combined with chemotherapy in this context remains largely unexplored, making this case significant.
Data Highlights
No numerical data available in the article.
Key Findings
A 52-year-old male with EGFR G719A mutation and extensive metastases showed a near-complete response to amivantamab plus chemotherapy.
Prior treatments included afatinib, pemetrexed/carboplatin, and a quadruple regimen, all of which failed to control disease progression.
Follow-up imaging indicated marked regression of lung mass, hepatic and brain metastases, and resolution of ascites.
The patient's performance status improved significantly and the response lasted over nine months with manageable side effects.
This case is the first to report a durable response to amivantamab in a patient with an uncommon EGFR mutation.
Clinical Implications
This case suggests that amivantamab combined with chemotherapy may be a viable salvage therapy for patients with EGFR G719A mutations and extensive visceral metastases. Clinicians should consider this combination for high-risk patients who have failed multiple lines of therapy, although further studies are needed to confirm these findings.
Conclusion
The observed durable response to amivantamab in this case underscores the potential of this treatment strategy in managing aggressive forms of EGFR-mutant lung cancer. Further research is warranted to validate these results in larger cohorts.