Key result
Third-line erlotinib linked to improved performance status and reduced peritoneal carcinomatosis lasting 9 months.
Why the study?
Does erlotinib improve outcomes in patients with peritoneal carcinomatosis from initially EGFR mutation-negative lung adenocarcinoma?
Case Report (n=1)
Does erlotinib improve outcomes in patients with peritoneal carcinomatosis from initially EGFR mutation-negative lung adenocarcinoma?
Erlotinib may provide significant clinical benefit in patients with lung adenocarcinoma and peritoneal carcinomatosis who are subsequently found to have EGFR mutations by immunohistochemistry, despite initial negative molecular testing.
May warrant IHC retesting for EGFR in peritoneal carcinomatosis from lung adenocarcinoma; hypothesis-generating for erlotinib benefit.
A woman in her late 50s with advanced lung adenocarcinoma, initially EGFR mutation-negative on single-plex testing, received cytotoxic chemotherapy and immune checkpoint inhibitors. After 1 year and 8 months, she developed peritoneal carcinomatosis. Third-line erlotinib led to an improvement in her performance status (PS 3 to 2 in 10 days) and a marked reduction in peritoneal carcinomatosis after 4 months, with the effect lasting for 9 months. Immunohistochemistry of the ascitic fluid revealed an EGFR L858R mutation. This case highlights the possibility of false-negative results on initial testing and suggests the potential benefit of EGFR-TKIs, even in EGFR mutation-negative cases at diagnosis.
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Fujimoto et al. (2026) conducted a case report in Advanced lung adenocarcinoma with peritoneal carcinomatosis (n=1). Erlotinib was evaluated on Improvement in performance status and reduction in peritoneal carcinomatosis. Third-line erlotinib led to an improvement in performance status from 3 to 2 in 10 days and a marked reduction in peritoneal carcinomatosis lasting 9 months.
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