Multi-institutional study of osimertinib dose-optimization in non-small cell lung cancer patients with EGFR activating mutation aged 70 years or older ('MONEY' trial).
Jpn J Clin Oncol
; 54(6): 730-734, 2024 Jun 01.
Article
en En
| MEDLINE
| ID: mdl-38520037
ABSTRACT
Osimertinib is the standard of care for patients with epidermal growth factor receptor-activating mutation-positive non-small cell lung cancer. Dose-toxicity has been previously reported, but no dose-response data within the range of 20-240 mg daily (mg/d). Thus, the current 80 mg/d dosing might be too high for elderly Japanese patients with an average body weight of only 50 kg, resulting in excessive toxicity and cost. We therefore initiated a study to investigate whether osimertinib at 40 mg/d is non-inferior to 80 mg/d in patients with advanced or recurrent epidermal growth factor receptor-activating mutation-positive non-small cell lung cancer aged ≥70 years, using a regression discontinuity design. Osimertinib is administered at 40 mg/d for body weight ≤50 kg, and 80 mg/d for body weight >50 kg. The primary endpoint is progression-free survival. Sample size is 550 patients, based on a non-inferiority margin of the progression-free survival hazard ratio 1.333, 0.10 one-sided type I error and 80% power.
Palabras clave
Texto completo:
1
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Acrilamidas
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Carcinoma de Pulmón de Células no Pequeñas
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Receptores ErbB
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Compuestos de Anilina
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Neoplasias Pulmonares
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Mutación
Límite:
Aged
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Aged80
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Female
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Humans
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Male
Idioma:
En
Revista:
Japanese journal of clinical oncology
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Jpn J Clin Oncol
/
Jpn. j. clin. oncol
Año:
2024
Tipo del documento:
Article
País de afiliación:
Japón