Literature DB >> 33491942

Association between peripheral eosinophils and clinical outcomes in patients with non-small cell lung cancer treated with immune checkpoint inhibitors.

Shinichiro Okauchi1, Toshihiro Shiozawa2, Kunihiko Miyazaki3, Kengo Nishino1, Yuika Sasatani1, Gen Ohara1, Katsunori Kagohashi1, Shinya Sato2, Takahide Kodama2, Hiroaki Satoh4, Nobuyuki Hizawa2.   

Abstract

INTRODUCTION: Programmed cell death ligand 1 is considered a predictor of the therapeutic effect of immune checkpoint inhibitors (ICPIs), but a more simple and useful predictor is needed.
OBJECTIVES: The aim of this study was to identify the relationship between eosinophil counts and percentages and response to ICPI therapy. PATIENTS AND METHODS: In 190 patients with non-small cell lung cancer (NSCLC) treated with ICPI therapy, peripheral eosinophil counts and percentages at the time of ICPI therapy initiation, the maximum counts and percentages of eosinophils during ICPI therapy, response to therapy, and time to treatment failure (TTF) were investigated.
RESULTS: Both an increase in the peripheral eosinophil count and an elevation of eosinophil percentage following the initiation of ICPI therapy were observed, regardless of whether the patients had controlled or progressive disease. The median time to the maximum eosinophil percentage was 5 weeks in patients with controlled disease and 2 weeks in those with progressive disease. The cutoff value for the maximum eosinophil counts and percentage during ICPI therapy was set at 300/μl and 5%, respectively, to identify the presence or absence of a therapeutic effect. Time to treatment failure was longer in patients with maximum eosinophil counts exceeding 300/μl and a maximum eosinophil percentage above 5%. In a multivariable analysis, a maximum eosinophil percentage of 5% during ICPI therapy was a significant predictive factor for therapeutic efficacy.
CONCLUSIONS: The measurement of peripheral eosinophils up to around 5 weeks following the initiation of treatment, especially the maximum eosinophils count and percentage, might provide useful information about the efficacy of ICPIs.

Entities:  

Year:  2021        PMID: 33491942     DOI: 10.20452/pamw.15776

Source DB:  PubMed          Journal:  Pol Arch Intern Med        ISSN: 0032-3772


  7 in total

1.  Absolute Increase in the Number and Proportion of Peripheral Eosinophils Associated With Immune Checkpoint Inhibitor Treatment in Non-small Cell Lung Cancer Patients.

Authors:  Hajime Osawa; Toshihiro Shiozawa; Shinichiro Okauchi; Yuika Sasatani; Gen Ohara; Shinya Sato; Kunihiko Miyazaki; Takahide Kodama; Katsunori Kagohashi; Hiroaki Satoh; Nobuyuki Hizawa
Journal:  Cancer Diagn Progn       Date:  2021-11-03

2.  Eosinophils Decrease Pulmonary Metastatic Mammary Tumor Growth.

Authors:  Rachel A Cederberg; Sarah Elizabeth Franks; Brennan J Wadsworth; Alvina So; Lisa R Decotret; Michael G Hall; Rocky Shi; Michael R Hughes; Kelly M McNagny; Kevin L Bennewith
Journal:  Front Oncol       Date:  2022-06-08       Impact factor: 5.738

Review 3.  Eosinophils and Lung Cancer: From Bench to Bedside.

Authors:  Anne Sibille; Jean-Louis Corhay; Renaud Louis; Vincent Ninane; Guy Jerusalem; Bernard Duysinx
Journal:  Int J Mol Sci       Date:  2022-05-03       Impact factor: 6.208

4.  The Association of Clinical Outcomes with Posttreatment Changes in the Relative Eosinophil Counts and Neutrophil-to-Eosinophil Ratio in Patients with Advanced Urothelial Carcinoma Treated with Pembrolizumab.

Authors:  Nobuki Furubayashi; Akinori Minato; Takahito Negishi; Naotaka Sakamoto; Yoohyun Song; Yoshifumi Hori; Toshihisa Tomoda; Shingo Tamura; Kentaro Kuroiwa; Narihito Seki; Naohiro Fujimoto; Motonobu Nakamura
Journal:  Cancer Manag Res       Date:  2021-10-24       Impact factor: 3.989

5.  Nivolumab and ipilimumab therapy in a patient with non-small cell lung cancer with chronic kidney disease.

Authors:  Hiroaki Satoh; Sou Hattori
Journal:  Contemp Oncol (Pozn)       Date:  2022-06-30

6.  Eosinophil as a biomarker for diagnosis, prediction, and prognosis evaluation of severe checkpoint inhibitor pneumonitis.

Authors:  Yanlin Li; Xiaohui Jia; Yonghao Du; Ziyang Mao; Yajuan Zhang; Yuan Shen; Hong Sun; Mengjie Liu; Gang Niu; Jun Wang; Jie Hu; Min Jiao; Hui Guo
Journal:  Front Oncol       Date:  2022-08-12       Impact factor: 5.738

7.  A robust CD8+ T cell-related classifier for predicting the prognosis and efficacy of immunotherapy in stage III lung adenocarcinoma.

Authors:  Jinteng Feng; Longwen Xu; Shirong Zhang; Luying Geng; Tian Zhang; Yang Yu; Rui Yuan; Yusheng He; Zhuhui Nan; Min Lin; Hui Guo
Journal:  Front Immunol       Date:  2022-08-31       Impact factor: 8.786

  7 in total

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