Expression patterns of novel immunotherapy targets in intermediate- and high-grade lung neuroendocrine neoplasms
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00843989%3A_____%2F24%3AE0110974" target="_blank" >RIV/00843989:_____/24:E0110974 - isvavai.cz</a>
Alternative codes found
RIV/61988987:17110/24:A2503AJR
Result on the web
<a href="https://link.springer.com/article/10.1007/s00262-024-03704-7" target="_blank" >https://link.springer.com/article/10.1007/s00262-024-03704-7</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s00262-024-03704-7" target="_blank" >10.1007/s00262-024-03704-7</a>
Alternative languages
Result language
angličtina
Original language name
Expression patterns of novel immunotherapy targets in intermediate- and high-grade lung neuroendocrine neoplasms
Original language description
Background: Advancements in immunotherapeutic approaches only had a modest impact on the therapy of lung neuroendocrine neoplasms (LNENs). Our multicenter study aimed to investigate the expression patterns of novel immunotherapy targets in intermediate- and high-grade LNENs. Methods: The expressions of V-domain Ig suppressor of T cell activation (VISTA), OX40L, Glucocorticoid-induced TNF receptor (GITR), and T cell immunoglobulin and mucin domain 3 (TIM3) proteins were measured by immunohistochemistry in surgically resected tumor samples of 26 atypical carcinoid (AC), 49 large cell neuroendocrine lung cancer (LCNEC), and 66 small cell lung cancer (SCLC) patients. Tumor and immune cells were separately scored. Results: Tumor cell TIM3 expression was the highest in ACs (p < 0.001), whereas elevated tumor cell GITR levels were characteristic for both ACs and SCLCs (p < 0.001 and p = 0.011, respectively). OX40L expression of tumor cells was considerably lower in ACs (vs. SCLCs; p < 0.001). Tumor cell VISTA expression was consistently low in LNENs, with no significant differences across histological subtypes. ACs were the least immunogenic tumors concerning immune cell abundance (p < 0.001). Immune cell VISTA and GITR expressions were also significantly lower in these intermediate-grade malignancies than in SCLCs or in LCNECs. Immune cell TIM3 and GITR expressions were associated with borderline prognostic significance in our multivariate model (p = 0.057 and p = 0.071, respectively). Conclusions: LNEN subtypes have characteristic and widely divergent VISTA, OX40L, GITR, and TIM3 protein expressions. By shedding light on the different expression patterns of these immunotherapy targets, the current multicenter study provides support for the future implementation of novel immunotherapeutic approaches.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30204 - Oncology
Result continuities
Project
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Continuities
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Others
Publication year
2024
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Cancer immunology, immunotherapy
ISSN
0340-7004
e-ISSN
1432-0851
Volume of the periodical
73
Issue of the periodical within the volume
article 114
Country of publishing house
DE - GERMANY
Number of pages
15
Pages from-to
1-15
UT code for WoS article
001225923900001
EID of the result in the Scopus database
2-s2.0-85191723943