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.

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.