دورية أكاديمية
Early changes in soluble intracellular adhesion molecule‐1 as prognostic biomarkers to immune checkpoint inhibitor
العنوان: | Early changes in soluble intracellular adhesion molecule‐1 as prognostic biomarkers to immune checkpoint inhibitor |
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المؤلفون: | Dongmei Ji, Shiyu Jiang, Qunling Zhang, Y. Ken Wang, Jian Zhang, Weina Shen, Wenhua Li, Rujiao Liu, Jessica Wang, Cory Mavis, Juan J. Gu, Xichun Hu |
المصدر: | Clinical and Translational Science, Vol 16, Iss 8, Pp 1396-1407 (2023) |
بيانات النشر: | Wiley, 2023. |
سنة النشر: | 2023 |
المجموعة: | LCC:Therapeutics. Pharmacology LCC:Public aspects of medicine |
مصطلحات موضوعية: | Therapeutics. Pharmacology, RM1-950, Public aspects of medicine, RA1-1270 |
الوصف: | Abstract Serologic biomarker to predict clinical outcome is needed for immune checkpoint inhibitors (ICIs). We evaluated soluble intercellular adhesion molecules‐1 (sICAM‐1) as a predictor of response to ICIs treatment. Ninety‐five patients with cancer treated with ICI were studied. The serum sICAM‐1 levels of baseline, post two cycle therapy and end of therapy (EOT) were measured by enzyme‐linked immunoassay. We randomly assigned the patients into the primary cohort (n = 47) and validation cohort (n = 48). Serum sICAM‐1 post two cycle (277.7 ± 181.6 ng/mL) and EOT (403.9 ± 218.9 ng/mL) were significantly elevated compared to baseline (244.8 ± 153.8 ng/mL, p = 0.008 and p = 0.004, respectively). Early changes of sICAM‐1 (ΔsICAM‐1), deemed as sICAM‐1 after two cycles minus baseline, were assessed. Following ICI treatments, responders had significantly lower ΔsICAM‐1 compared with nonresponders in the primary cohort (p = 0.040) and the validation cohort (p = 0.026). High ΔsICAM‐1 was strongly associated with inferior progression‐free survival (PFS; (primary cohort: p = 0.001 and validation cohort: p = 0.002) and overall survival (OS; (primary cohort: p |
نوع الوثيقة: | article |
وصف الملف: | electronic resource |
اللغة: | English |
تدمد: | 1752-8062 1752-8054 |
Relation: | https://doaj.org/toc/1752-8054; https://doaj.org/toc/1752-8062 |
DOI: | 10.1111/cts.13540 |
URL الوصول: | https://doaj.org/article/b3bf6dc625e243009db43c8ca3711a57 |
رقم الأكسشن: | edsdoj.b3bf6dc625e243009db43c8ca3711a57 |
قاعدة البيانات: | Directory of Open Access Journals |
تدمد: | 17528062 17528054 |
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DOI: | 10.1111/cts.13540 |