Impact of tumor microenvironment on the efficacy of epidermal growth factor receptor‐tyrosine kinase inhibitors in patients withEGFR‐mutant non‐small cell lung cancer

التفاصيل البيبلوغرافية
العنوان: Impact of tumor microenvironment on the efficacy of epidermal growth factor receptor‐tyrosine kinase inhibitors in patients withEGFR‐mutant non‐small cell lung cancer
المؤلفون: Jun Oyanagi, Tetsuya Watanabe, Koichi Ogawa, Mitsuru Fukui, Hiroyasu Kaneda, Tomoya Kawaguchi, Yasuhiro Koh, Yoshiya Matsumoto, Tomohiro Suzumura, Tatsuo Kimura, Shigeki Mitsuoka, Kenji Sawa, Nobuyuki Yamamoto, Motohiro Izumi, Kazuhisa Asai
المصدر: Cancer Science
بيانات النشر: Wiley, 2019.
سنة النشر: 2019
مصطلحات موضوعية: Male, 0301 basic medicine, epidermal growth factor receptor tyrosine kinase inhibitor, Cancer Research, Lung Neoplasms, Cell, Gastroenterology, B7-H1 Antigen, 0302 clinical medicine, Japan, Carcinoma, Non-Small-Cell Lung, Tumor Microenvironment, Medicine, Epidermal growth factor receptor, Aged, 80 and over, education.field_of_study, biology, Kinase, General Medicine, Middle Aged, ErbB Receptors, Treatment Outcome, medicine.anatomical_structure, Oncology, 030220 oncology & carcinogenesis, Immunohistochemistry, Original Article, Female, Programmed cell death 1 ligand 2, non‐small cell lung cancer, Adult, medicine.medical_specialty, CD8 Antigens, 03 medical and health sciences, Lymphocytes, Tumor-Infiltrating, Clinical Research, Internal medicine, Humans, Lung cancer, education, Protein Kinase Inhibitors, Aged, Retrospective Studies, Tumor microenvironment, business.industry, Original Articles, programmed cell death‐1 ligand‐1, Programmed Cell Death 1 Ligand 2 Protein, medicine.disease, programmed cell death‐1 ligand‐2, Survival Analysis, 030104 developmental biology, Mutation, biology.protein, business, CD8
الوصف: We retrospectively investigated the impact of the tumor microenvironment (TME) on the efficacy of epidermal growth factor receptor (EGFR)‐tyrosine kinase inhibitors (TKIs) as first‐line treatment in 70 patients with advanced EGFR‐mutant non‐small cell lung cancer and who were seen at Osaka City University Hospital (Osaka, Japan) between August 2013 and December 2017. Using immunohistochemical staining with 28‐8 and D7U8C Abs, the tumor proportion score was assessed for programmed cell death‐1 ligand‐1 (PD‐L1), as high (50% or more) or low (less than 50%), and ligand‐2 (PD‐L2) expression, respectively. The extent of CD8+ tumor‐infiltrating lymphocytes was evaluated on a scale of 0‐3, with 0‐1 as low and 2‐3 as high. The TME of the 52 evaluable pretreatment specimens was categorized into 4 subtypes, according to the respective PD‐L1 tumor proportion and CD8+ scores, as follows: (a) high/high (13.5%, n = 7); (b) low/low (42.3%, n = 22); (c) high/low (17.3%, n = 9); and (d) low/high (26.9%, n = 14). Expression of PD‐L2 was significantly the highest in type 1 (57.1% vs 4.5% vs 11.1% vs 7.1%, respectively; P = .0090). Response rate was significantly the lowest in type 1 (14.3% vs 81.8% vs 66.7% vs 78.6%, respectively; P = .0085). Progression‐free survival was the shortest in type 1 and the longest in type 4 (median, 2.4 vs 11.3 vs 8.4 vs 17.5 months, respectively; P = .00000077). The efficacy of EGFR‐TKIs differed according to the TME, and the phenotype with high PD‐L1 and CD8+ expression might be the subset that would poorly benefit from such treatment.
تدمد: 1349-7006
1347-9032
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb74ba3d7bb8d4caf8b67643a7c49790Test
https://doi.org/10.1111/cas.14156Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....cb74ba3d7bb8d4caf8b67643a7c49790
قاعدة البيانات: OpenAIRE