scholarly journals 40P Correlation of IL-1-β-serum concentration with the number of leukocytes in peripheral blood in patients with solid tumours before immune checkpoint inhibitors therapy

2020 ◽  
Vol 31 ◽  
pp. S1229
Author(s):  
A.M. Malkova ◽  
R.V. Orlova ◽  
N.V. Zhukova ◽  
V.V. Sharoyko ◽  
E.A. Kaledina ◽  
...  
ESMO Open ◽  
2019 ◽  
Vol 4 (1) ◽  
pp. e000457 ◽  
Author(s):  
Giovanni Fucà ◽  
Giulia Galli ◽  
Marta Poggi ◽  
Giuseppe Lo Russo ◽  
Claudia Proto ◽  
...  

BackgroundSteroids are frequently used in patients with metastatic non-small cell lung cancer (mNSCLC), but they could be detrimental for patients treated with immune checkpoint inhibitors (ICIs). Here, we assessed the association between early use of steroids, clinical outcomes and peripheral immune blood cells modulation in patients with mNSCLC treated with ICIs.MethodsWe reviewed patients with mNSCLC treated at our institution between April 2013 and December 2017. Early use of steroids was defined as the use of a daily prednisone-equivalent dose ≥10 mg for at least 1 day within 28 days after ICI initiation. Peripheral immune blood cell counts were retrieved at baseline and at 4 and 6 weeks after ICI initiation.ResultsOut of 151 patients included, 35 (23%) made early use of steroids that was associated with poor disease control (OR 0.32, p=0.006), progression-free survival (HR 1.80, p=0.003) and overall survival (HR 2.60, p<0.001). Early use of steroids significantly correlated with higher median absolute neutrophil count, neutrophil to lymphocyte ratio (NLR) and derived NLR, and lower median absolute and relative eosinophil count, both at 4 and 6 weeks after ICI initiation.ConclusionsIn patients with mNSCLC treated with ICIs, early use of steroids was associated with worse clinical outcomes and remarkable modulation of peripheral blood immune cells, which could contribute to restraining the activation of antitumour immunity. If confirmed in prospective studies, these findings would highlight the importance of carefully evaluating and, whenever possible, avoiding steroids during early phases of ICI treatment.


2021 ◽  
pp. 1-7
Author(s):  
Laura Haik ◽  
Aurore Gonthier ◽  
Amandine Quivy ◽  
Marine Gross-goupil ◽  
Remi Veillon ◽  
...  

2020 ◽  
Vol 31 ◽  
pp. S714
Author(s):  
M. Maugeais ◽  
J. Peron ◽  
S. Dalle ◽  
M. Duruisseaux ◽  
P. Corbaux ◽  
...  

2019 ◽  
Vol 30 ◽  
pp. v519-v520
Author(s):  
F J Ros Montana ◽  
I. Matos ◽  
G. Vilacampa ◽  
A. Azaro ◽  
J. Martin-Liberal ◽  
...  

2021 ◽  
Vol 8 (3) ◽  
pp. 34-43
Author(s):  
A. A. Musaelyan ◽  
A. L. Akopov ◽  
S. V. Lapin ◽  
V. D. Nazarov ◽  
D. I. Fillipov ◽  
...  

Immune checkpoint inhibitors (ICIs) alone or in combination with chemotherapy have become one of the key approaches in the treatment of patients with advanced non-small cell lung cancer (NSCLC). Evaluation of level of PD-L1 (ligand of the programmed cell death receptor 1) expression on tumor cells using immunohistochemistry is the only approved option for determining the indications of ICIs in this group of patients. However, despite high level of PD-L1 expression, up to 80 % of patients do not respond to therapy due to the presence of primary or acquired resistance, which determines the limited effectiveness of ICI. In addition, 8–17 % of PD-L1-negative patients with NSCLC are also able to respond to ICIs. The limitation of this marker is that it does not allow assessing both intratumoral and systemic immune status. It is necessary to search for additional predictive markers to improve the accuracy of the selection of candidates for immunotherapy, which will avoid costs, wasted time, and a high risk of immune-related adverse events in potentially unresponsive patients. The attention of researchers is devoted to circulating markers in peripheral blood, as a non-invasive alternative to biopsy for predicting and monitoring the response. This review focuses on the most promising immunological markers in peripheral blood as potential predictors of response to ICIs in patients with advanced NSCLC.


2019 ◽  
Vol 30 ◽  
pp. v524-v525
Author(s):  
S. Mebarki ◽  
M. Gisselbrecht ◽  
E. Fabre ◽  
E. Mercadier ◽  
S. Oudard ◽  
...  

Life ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1400
Author(s):  
Alejandro Olivares-Hernández ◽  
Luis Figuero-Pérez ◽  
José Pablo Miramontes-González ◽  
Álvaro López-Gutiérrez ◽  
Rogelio González-Sarmiento ◽  
...  

The relationship between viral infections and cancer is well known and has been established for decades. Multiple tumours are generated from alterations secondary to viral infections 2 resulting from a dysregulation of the immune system in many cases. Certain causal relationships, such as that between the Epstein–Barr virus (EBV) in nasopharyngeal cancer or hepatitis C and B viruses in hepatocarcinoma, have been clearly established, and their implications for the prognosis and treatment of solid tumours are currently unknown. Multiple studies have evaluated the role that these infections may have in the treatment of solid tumours using immunotherapy. A possible relationship between viral infections and an increased response to immune checkpoint inhibitors (ICIs) has been established at a theoretical level in solid neoplasms, such as EBV-positive cavum cancer and human papillomavirus (HPV)-positive and oropharyngeal cancer. These could yield a greater response associated with the activation of the immune system secondary to viral infection, the consequence of which is an increase in survival in these patients. That is why the objective of this review is to assess the different studies or clinical trials carried out in patients with solid tumours secondary to viral infections and their relationship to the response to ICIs.


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