Cancer Treatment and Research Communications | 卷:32 |
Absolute eosinophil count predicts clinical outcomes and toxicity in non-small cell lung cancer patients treated with immunotherapy | |
Francesca Mazzoni1  Sara Fancelli1  Lorenzo Antonuzzo2  Carlotta Ottanelli3  Enrico Caliman3  Marta Rita Gatta Michelet3  Elisa Giommoni3  Serena Pillozzi4  Federico Scolari5  Daniele Lavacchi5  Brunella Napolitano5  Luca Voltolini5  Luca Paglialunga5  Camilla Eva Comin5  | |
[1] Department of Experimental and Clinical Medicine, University of Florence, Italy; | |
[2] Thoracic Surgery Unit, Careggi University Hospital, Florence, Italy; | |
[3] Clinical Oncology Unit, Careggi University Hospital, Florence, Italy; | |
[4] Medical Oncology Unit, Careggi University Hospital, Florence, Italy; | |
关键词: Non-small cell lung cancer; Immunotherapy; Eosinophils; Absolute eosinophil count; Biomarker; | |
DOI : | |
来源: DOAJ |
【 摘 要 】
Objectives: Immune checkpoint inhibitors (ICIs) have led to a paradigm shift in non-small cell lung cancer (NSCLC) treatment. We investigated absolute eosinophil count (AEC) as a predictor of clinical outcomes and toxicity in NSCLC patients receiving ICIs. Materials and Methods: AEC was retrospectively collected at baseline and during treatment from 158 advanced NSCLC patients treated with single agent anti-PD1/anti-PDL1 monoclonal antibody in first or subsequent line of therapy at Medical Oncology Unit, Careggi University Hospital, Florence (Italy), between January 2016 to October 2020. Results: We found a significant association between high baseline AEC (≥130/μL) and better clinical outcomes. The response rates were 64.4% and 35.6% for patients with high and low AEC, respectively (p = 0.009). The high-AEC group showed a significantly longer PFS and OS than the low-AEC group (mPFS = 7.0 months, 95% CI 5.0–10.0 vs 2.5 months, 95% CI 2.0–4.0, p = 0.007 and mOS = 9.0 months, CI 95% 7.0–15.0 vs 5.5 months, 95% CI 4.0–8.0, p = 0.009, respectively). An increased risk of immune-related adverse events (irAEs) was reported in the high-AEC group (p = 0.133). IrAEs resulted an independent prognostic factor for both better outcomes (mPFS = 8.0 months, 95% CI 7.0–12.0 vs 2.0 months, 95% CI 2.0–3.0, p<0.001; mOS = 13.0 months 95% CI 9.0–19.0 vs 4.0 months 95% CI 3.0–6–0, p<0.001) and response to ICIs (response rate = 33.8% vs 14.9%, disease control rate = 72.0% vs 32.1%, p<0.001). Conclusion: High baseline AEC value (≥130/μL) is a predictive biomarker of clinical benefit and irAEs occurrence in NSCLC patients treated with ICIs.
【 授权许可】
Unknown