Treatment of NSCLC With Uncommon EGFR Mutations Treatment of NSCLC With Uncommon EGFR Mutations
A female patient, Chinese descent, aged 66, is referred from primary care with persistent cough, sputum with blood, shortness of breath and chest pain HistoryNever smoked Recurrent bronchitis over past 5 years Has never been screened for lung cancer (by radiography or low-dose CT [LDCT]) Hypertension controlled on HCTZ; no diabetes, renal impairment Family historyGrew up in China, moved to US at age 29; married for 30 years Grew up in family with heavy smokers Husband is current smoker LDCT reveals multiple tumors in left lung with pleural metastases Biopsy reveals non-small cell lung cancer Molecular analysis:EGFR mutation: G719XNegative forALK rearrangement Wild-typeKRAS The patient was started on afatinib, 40 mg once daily After one month on therapy, she reported having rather severe diarrhea (5 times/day) Treatment was discontinued, then re-started treatment at 30 mg/day Newsletter Stay up to date on practice-changing data in community practice.
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September 17th, 2026 The COPERNICUS study of amivantamab/lazertinib showed lower rates of adverse events and discontinuation with supportive care regimens in patients with EGFR-mutated non–small cell lung cancer.
September 21st, 2026 Updated TRUST-I and TRUST-II data show durable taletrectinib responses in ROS1+ NSCLC regardless of prior chemotherapy or fusion partner.
September 17th, 2026 The FDA approved an sNDA updating the taletrectinib label with a 49.7-month median duration of response from TRUST-I in ROS1-positive NSCLC.
September 25th, 2026 US cancer deaths keep falling as lung cancer declines; smoking drops, screening rises, but rural and low-education gaps persist.
September 19th, 2026 David DiBardino, MD, explains how intratumoral radioenhancer therapy works, why standardization remains a challenge, and what early CONVERGE study data suggest for locally advanced NSCLC.