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Published on: August 11, 2017
Response of EGFR-mutated pulmonary pleomorphic carcinoma to pembrolizumab
Yuki Hatakeyama1, Hidenori Mizugaki1, Noriyuki Yamada1
1Department of Respiratory Medicine, NHO Hokkaido Cancer Center, Sapporo, Japan.
Abstract:
Pulmonary pleomorphic carcinoma (PPC) is a rare and aggressive lung malignancy with limited treatment options. While immune checkpoint inhibitors (ICIs) have shown promise in treating PPC, evidence regarding their efficacy in epidermal growth factor receptor (EGFR)-mutated cases remains scarce. We report a case of a woman in her 70s diagnosed with PPC harboring EGFR L858R + E709K mutations and high expression (95 %) of programmed death-ligand 1 (PD-L1). After relapsing from concurrent chemoradiotherapy for a Pancoast tumor, the patient received osimertinib as second-line therapy. Despite an initial response, rapid disease progression necessitated left lower lobectomy, confirming PPC diagnosis. Subsequent treatment with pembrolizumab achieved notably tumor response. Although Grade 3 immune-related colitis developed, it was successfully managed with prednisolone, allowing completion of six courses of pembrolizumab. This case demonstrates the potential efficacy of ICIs in EGFR-mutated PPC, even after epidermal growth factor receptor -tyrosine kinase inhibitor (EGFR-TKI) failure and highlights the importance of appropriate adverse event management. Our findings suggest that ICIs may be a viable treatment option for EGFR-mutated PPC patients, particularly those with high PD-L1 expression.
Insights
Immune checkpoint inhibitors show promise for pulmonary pleomorphic carcinoma (PPC) with EGFR mutations. This case highlights their potential efficacy after targeted therapy failure, even with severe side effects.
Area of Science:
- Oncology
- Pulmonology
- Immunotherapy
Background:
- Pulmonary pleomorphic carcinoma (PPC) is a rare, aggressive lung cancer with limited treatment options.
- Evidence for immune checkpoint inhibitors (ICIs) in EGFR-mutated PPC is scarce.
- High programmed death-ligand 1 (PD-L1) expression is noted in some PPC cases.
Observation:
- A case of a woman in her 70s with EGFR-mutated PPC (L858R + E709K) and high PD-L1 expression (95%) is presented.
- The patient experienced disease progression after concurrent chemoradiotherapy and initial response to osimertinib (an EGFR-TKI).
- Following left lower lobectomy, pembrolizumab (an ICI) treatment led to a notable tumor response.
Findings:
- Pembrolizumab demonstrated efficacy in an EGFR-mutated PPC patient post-EGFR-TKI failure.
- High PD-L1 expression (95%) correlated with response to immunotherapy.
- Immune-related adverse events (Grade 3 colitis) were manageable with prednisolone.
Implications:
- ICIs represent a potential therapeutic strategy for EGFR-mutated PPC, especially in cases with high PD-L1 expression.
- This case underscores the importance of managing immune-related adverse events for successful ICI therapy.
- Further research is warranted to explore ICI efficacy in this specific patient subgroup.
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