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The predictive potential of autoimmune-inflammatory syndrome induced by adjuvants (ASIA) criteria to assess the risk of adverse events and efficacy of immune checkpoint inhibitor therapy. / Zhukova, Natalia; Orlova, Rashida; Malkova, Anna; Kaledina, Ekaterina; Demchenkova, Alexandra; Percik, Ruth; Shoenfeld, Yehuda.

в: Immunologic Research, Том 70, 01.01.2022, стр. 765–774.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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@article{1a40bef58b2749e38049716a22b4b80b,
title = "The predictive potential of autoimmune-inflammatory syndrome induced by adjuvants (ASIA) criteria to assess the risk of adverse events and efficacy of immune checkpoint inhibitor therapy",
abstract = "At the moment, there are no approved predictive markers of immune adverse events (irAES) induced by immune checkpoint inhibitors (ICIs) and the treatment efficacy. The early stages of irAES have some similarities with adjuvant-induced autoimmune/pro-inflammatory syndrome (ASIA). This study aims to assess the predictive possibility of using the “ASIA questionnaire” in patients on immune checkpoint inhibitor therapy in comparison with determination of PD-L1 expression to predict the risk of irAES development and therapy efficacy. We examined patients (n = 91) being treated for solid tumors. The signs of ASIA were found in 74% (66/91), while ASIA syndrome was diagnosed in 54% of cases (49/91). No statistically significant difference in the frequency of ICI-dependent complication development regarding the presence of previous ASIA clinical manifestations, hereditary factors, sex, different trigger factors was found. Index based on combination of PD-L1 determination and ASIA index was created. With reference > 2.5 units, the disease control rate (DCR) could be predicted with sensitivity 100.0% and specificity 70.00%, p = 0.007. The study did not reveal the diagnostic value of ASIA questionnaire to assess the risk of adverse events; however, in early stages, the development of ASIA symptoms diagnosed with the questionnaire in complex with PD-L1 expression allowed to predict a treatment efficacy.",
keywords = "Autoimmune-inflammatory syndrome induced by adjuvants (ASIA), Immune adverse events (irAES), Immune checkpoint inhibitors (ICI), Predictive factors, Triggers",
author = "Natalia Zhukova and Rashida Orlova and Anna Malkova and Ekaterina Kaledina and Alexandra Demchenkova and Ruth Percik and Yehuda Shoenfeld",
year = "2022",
month = jan,
day = "1",
doi = "10.1007/s12026-022-09304-w",
language = "English",
volume = "70",
pages = "765–774",
journal = "Immunologic Research",
issn = "0257-277X",
publisher = "Humana Press",

}

RIS

TY - JOUR

T1 - The predictive potential of autoimmune-inflammatory syndrome induced by adjuvants (ASIA) criteria to assess the risk of adverse events and efficacy of immune checkpoint inhibitor therapy

AU - Zhukova, Natalia

AU - Orlova, Rashida

AU - Malkova, Anna

AU - Kaledina, Ekaterina

AU - Demchenkova, Alexandra

AU - Percik, Ruth

AU - Shoenfeld, Yehuda

PY - 2022/1/1

Y1 - 2022/1/1

N2 - At the moment, there are no approved predictive markers of immune adverse events (irAES) induced by immune checkpoint inhibitors (ICIs) and the treatment efficacy. The early stages of irAES have some similarities with adjuvant-induced autoimmune/pro-inflammatory syndrome (ASIA). This study aims to assess the predictive possibility of using the “ASIA questionnaire” in patients on immune checkpoint inhibitor therapy in comparison with determination of PD-L1 expression to predict the risk of irAES development and therapy efficacy. We examined patients (n = 91) being treated for solid tumors. The signs of ASIA were found in 74% (66/91), while ASIA syndrome was diagnosed in 54% of cases (49/91). No statistically significant difference in the frequency of ICI-dependent complication development regarding the presence of previous ASIA clinical manifestations, hereditary factors, sex, different trigger factors was found. Index based on combination of PD-L1 determination and ASIA index was created. With reference > 2.5 units, the disease control rate (DCR) could be predicted with sensitivity 100.0% and specificity 70.00%, p = 0.007. The study did not reveal the diagnostic value of ASIA questionnaire to assess the risk of adverse events; however, in early stages, the development of ASIA symptoms diagnosed with the questionnaire in complex with PD-L1 expression allowed to predict a treatment efficacy.

AB - At the moment, there are no approved predictive markers of immune adverse events (irAES) induced by immune checkpoint inhibitors (ICIs) and the treatment efficacy. The early stages of irAES have some similarities with adjuvant-induced autoimmune/pro-inflammatory syndrome (ASIA). This study aims to assess the predictive possibility of using the “ASIA questionnaire” in patients on immune checkpoint inhibitor therapy in comparison with determination of PD-L1 expression to predict the risk of irAES development and therapy efficacy. We examined patients (n = 91) being treated for solid tumors. The signs of ASIA were found in 74% (66/91), while ASIA syndrome was diagnosed in 54% of cases (49/91). No statistically significant difference in the frequency of ICI-dependent complication development regarding the presence of previous ASIA clinical manifestations, hereditary factors, sex, different trigger factors was found. Index based on combination of PD-L1 determination and ASIA index was created. With reference > 2.5 units, the disease control rate (DCR) could be predicted with sensitivity 100.0% and specificity 70.00%, p = 0.007. The study did not reveal the diagnostic value of ASIA questionnaire to assess the risk of adverse events; however, in early stages, the development of ASIA symptoms diagnosed with the questionnaire in complex with PD-L1 expression allowed to predict a treatment efficacy.

KW - Autoimmune-inflammatory syndrome induced by adjuvants (ASIA)

KW - Immune adverse events (irAES)

KW - Immune checkpoint inhibitors (ICI)

KW - Predictive factors

KW - Triggers

UR - http://www.scopus.com/inward/record.url?scp=85133353552&partnerID=8YFLogxK

U2 - 10.1007/s12026-022-09304-w

DO - 10.1007/s12026-022-09304-w

M3 - Article

AN - SCOPUS:85133353552

VL - 70

SP - 765

EP - 774

JO - Immunologic Research

JF - Immunologic Research

SN - 0257-277X

ER -

ID: 116163908