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Biological Difference between L858R and Exon 19 Deletion Contributes to Recurrence-Free Survival of Resected Non-Small Cell Lung Cancer.
Masago, Katsuhiro; Kuroda, Hiroaki; Fujita, Shiro; Sasaki, Eiichi; Takahashi, Yusuke; Shinohara, Shuichi; Matsushita, Hirokazu.
  • Masago K; Department of Pathology and Molecular Diagnostics, Aichi Cancer Center, Nagoya, Japan.
  • Kuroda H; Department of Respiratory Surgery, Aichi Cancer Center Hospital, Nagoya, Japan.
  • Fujita S; Department of Respiratory Medicine, Kobe Central Hospital, Kobe, Japan.
  • Sasaki E; Department of Pathology and Molecular Diagnostics, Aichi Cancer Center, Nagoya, Japan.
  • Takahashi Y; Department of Respiratory Surgery, Aichi Cancer Center Hospital, Nagoya, Japan.
  • Shinohara S; Department of Respiratory Surgery, Aichi Cancer Center Hospital, Nagoya, Japan.
  • Matsushita H; Division of Translational Oncoimmunology, Aichi Cancer Research Institute, Nagoya, Japan.
Oncology ; 101(2): 117-125, 2023.
Article en En | MEDLINE | ID: mdl-36099878
INTRODUCTION: The differences in biological characteristics among different genotypes of classical EGFR mutations have not been clarified. This study aimed to clarify the clinical and biological differences between L858R and 19 deletion in NSCLC. METHODS: We analyzed a cohort of 191 consecutive cases of surgically resected NSCLC harboring EGFR driver mutations (L858R or 19 deletion) in which curative resection was performed in Aichi Cancer Center Hospital, Nagoya, Japan, from January 2006 to September 2021 and in which recurrence subsequently developed. We also subjected 61 surgically resected NSCLC specimens harboring EGFR driver mutations (L858R or 19 deletion) to an RNA sequencing analysis. RESULTS: In patients with stage I disease, the median time to recurrence did not differ to a statistically significant extent between the types of EGFR mutations; however, among those with stage II and III disease, the median time to recurrence in patients with the L858R genotype tended to be shorter in comparison to those with 19 deletion (log-rank test, p = 0.47 and 0.46, respectively). In comparison to 19 deletion tumors, L858R tumors had higher cytological malignancy (e.g., mitotic ability) and showed stronger immunogenicity. CONCLUSION: L858R and 19 deletion tumors are likely to have a slight difference in the time to recurrence. They suggest that even in EGFR driver tumors, which are treated as the same disease category, the biological characteristics of the tumors are different, which may leave room for innovations in postoperative treatment and treatment at recurrence.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article