Mutation profile and programmed death ligand 1 status of patients with non-small cell lung cancer diagnosed with "adenocarcinoma" and "non-small cell carcinoma favor adenocarcinoma"

© 2024 The Authors. Thoracic Cancer published by John Wiley & Sons Australia, Ltd..

BACKGROUND: The terminology for lung cancer diagnosis in small biopsies was adopted in the 2015 World Health Organization classification. If non-small cell lung cancer (NSCLC) has no clear adenocarcinoma (AD) or squamous cell carcinoma morphology, the tumor is further classified based on mucin or immunohistochemical staining as NSCLC favor AD (NFAD), NSCLC favor squamous cell carcinoma, or NSCLC not otherwise specified. Since this new term was defined, the difference between AD and NFAD has not yet been fully explored. This study aimed to examine the differences in clinical background, gene alteration frequency, and programmed death ligand 1 (PD-L1) expression.

METHODS: We included patients diagnosed with AD or NFAD with small samples, and who underwent testing with the Oncomine Dx target test between August 2019 and April 2023 in Kanagawa Cancer Center.

RESULTS: This study comprised 268 patients. A total of 96 patients underwent surgery after AD or NFAD diagnosis. The clinical stage was more advanced and pathological N0 was lower in NFAD than in AD. The pathology of the surgical specimens revealed that solid predominant AD was significantly more common in NFAD than in AD (p < 0.001). In both AD and NFAD, EGFR mutation was the most frequent gene alteration, followed by KRAS mutation. The frequency of EGFR mutations was significantly higher in AD than in NFAD. PD-L1 expression was significantly higher in NFAD than in AD (p < 0.001).

CONCLUSION: This study shows a clear difference between AD and NFAD in terms of cancer progression, pathological features of the main tumor, genetic characteristics, and PD-L1 expression.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:15

Enthalten in:

Thoracic cancer - 15(2024), 6 vom: 11. Feb., Seite 458-465

Sprache:

Englisch

Beteiligte Personen:

Shigeta, Naoko [VerfasserIn]
Yokose, Tomoyuki [VerfasserIn]
Murakami, Shuji [VerfasserIn]
Isaka, Tetsuya [VerfasserIn]
Shinada, Kanako [VerfasserIn]
Yoshioka, Emi [VerfasserIn]
Narita, Atsuya [VerfasserIn]
Katakura, Kengo [VerfasserIn]
Kondo, Tetsuro [VerfasserIn]
Kato, Terufumi [VerfasserIn]
Nagashima, Takuya [VerfasserIn]
Saito, Haruhiro [VerfasserIn]
Ito, Hiroyuki [VerfasserIn]

Links:

Volltext

Themen:

B7-H1 Antigen
Biopsy
CD274 protein, human
EC 2.7.10.1
Epidermal growth factor receptor (EGFR)
ErbB Receptors
Journal Article
Next-generation sequencing panel
Non-small cell lung cancer
Programmed death ligand 1 (PD-L1)

Anmerkungen:

Date Completed 26.02.2024

Date Revised 27.02.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1111/1759-7714.15214

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM366877607