Literature DB >> 35106186

Effect of pretreatment with dexamethasone on the efficacy and immune-related adverse events of immunotherapy in first-line treatment for advanced non-small cell lung cancer: a network meta-analysis of randomized control trials.

Yanwei Li1,2,3, Feng He1,2, Shuang Liu1,2, Yu Zhang3, Ling Li3, Bin Wang3, Lan Lan3, Zhanyu Pan3.   

Abstract

BACKGROUND: The pretreatment of dexamethasone on the efficacy and immune-related adverse events of immunotherapy involving programmed cell death 1/programmed cell death 1 ligand 1 (PD1/PDL1) inhibitors is an effective option for the first-line treatment of advanced non-small-cell lung cancer (NSCLC). With the immunosuppressive effect, corticosteroids may be used to reduce the efficacy of PDL1 blockade, as well as prevent overactive immune responses, thereby reducing the occurrence of immune-related adverse events (irAEs). This study quantitatively summarized the current evidence, and compared the efficacy and toxicity of therapies involving chemotherapy plus PDL1 inhibitors plus dexamethasone pretreatment (I+C+D) with chemotherapy plus PDL1 inhibitors (I+C) and therapies involving PDL1 inhibitors or chemotherapy alone (I or C).
METHODS: The protocol of this study was registered with PROSPERO (CRD42021227281). By using a network meta-analysis approach, the different treatments were compared and ranked based on their effectiveness and rates of irAEs at the different grades. Risk rates were determined through direct meta-analysis and indirect treatment comparison.
RESULTS: 12 randomized clinical trials were included with a total of 7155 NSCLC patients. Network meta-analysis generated 15 comparisons. The combination treatment of I+C+D showed a longer progression-free survival and overall survival, while I+C was less toxic, and the toxicity of I+C+D or that of I+C had been significantly decreased, compared to that of monotherapy with either drug. According to the ranking analysis, I+C+D is consistently proved to be the most effective therapeutic strategy, while I+C is linked to the lowest rate of irAEs, with the rate of grade value of ≥3 irAEs.
CONCLUSION: The combination treatment of I+C+D is the most effective approach for the first-line treatment of NSCLC patients treated with I+C, I, or C. AJCEI
Copyright © 2021.

Entities:  

Keywords:  Dexamethasone; immunotherapy; network meta-analysis

Year:  2021        PMID: 35106186      PMCID: PMC8784760     

Source DB:  PubMed          Journal:  Am J Clin Exp Immunol


  26 in total

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Review 3.  Immune-related adverse events from combination immunotherapy in cancer patients: A comprehensive meta-analysis of randomized controlled trials.

Authors:  Bo Zhang; Qiong Wu; You Lang Zhou; Xinyu Guo; Jun Ge; Jiaji Fu
Journal:  Int Immunopharmacol       Date:  2018-08-18       Impact factor: 4.932

4.  [The Version 2.0 Practice Guideline for Anti-Emetic and Standard Therapy].

Authors:  Toshiaki Saeki
Journal:  Gan To Kagaku Ryoho       Date:  2019-11

5.  Immune Checkpoint Inhibitor Outcomes for Patients With Non-Small-Cell Lung Cancer Receiving Baseline Corticosteroids for Palliative Versus Nonpalliative Indications.

Authors:  Biagio Ricciuti; Suzanne E Dahlberg; Anika Adeni; Lynette M Sholl; Mizuki Nishino; Mark M Awad
Journal:  J Clin Oncol       Date:  2019-06-17       Impact factor: 44.544

6.  Camrelizumab plus carboplatin and pemetrexed versus chemotherapy alone in chemotherapy-naive patients with advanced non-squamous non-small-cell lung cancer (CameL): a randomised, open-label, multicentre, phase 3 trial.

Authors:  Caicun Zhou; Gongyan Chen; Yunchao Huang; Jianying Zhou; LiZhu Lin; Jifeng Feng; Zhehai Wang; Yongqian Shu; Jianhua Shi; Yi Hu; QiMing Wang; Ying Cheng; Fengying Wu; Jianhua Chen; Xiaoyan Lin; Yongsheng Wang; Jianan Huang; Jiuwei Cui; Lejie Cao; Yunpeng Liu; Yiping Zhang; Yueyin Pan; Jun Zhao; LiPing Wang; Jianhua Chang; Qun Chen; Xiubao Ren; Wei Zhang; Yun Fan; Zhiyong He; Jian Fang; Kangsheng Gu; XiaoRong Dong; Tao Zhang; Wei Shi; Jianjun Zou
Journal:  Lancet Respir Med       Date:  2020-12-18       Impact factor: 30.700

7.  Pemetrexed for heavily pretreated patients with advanced non-small cell lung cancer.

Authors:  Jih-Hsiang Lee; Chong-Jen Yu; Kuan-Yu Chen; Jin-Yuan Shih; Yu-Lin Lin; Chih-Hsin Yang
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8.  Efficacy and Safety of Sintilimab Plus Pemetrexed and Platinum as First-Line Treatment for Locally Advanced or Metastatic Nonsquamous NSCLC: a Randomized, Double-Blind, Phase 3 Study (Oncology pRogram by InnovENT anti-PD-1-11).

Authors:  Yunpeng Yang; Zhehai Wang; Jian Fang; Qitao Yu; Baohui Han; Shundong Cang; Gongyan Chen; Xiaodong Mei; Zhixiong Yang; Rui Ma; Minghong Bi; Xiubao Ren; Jianying Zhou; Baolan Li; Yong Song; Jifeng Feng; Juan Li; Zhiyong He; Rui Zhou; Weimin Li; You Lu; Yingyi Wang; Lijun Wang; Nong Yang; Yan Zhang; Zhuang Yu; Yanqiu Zhao; Conghua Xie; Ying Cheng; Hui Zhou; Shuyan Wang; Donglei Zhu; Wen Zhang; Li Zhang
Journal:  J Thorac Oncol       Date:  2020-08-08       Impact factor: 15.609

9.  Chemotherapy in Combination With Immune Checkpoint Inhibitors for the First-Line Treatment of Patients With Advanced Non-small Cell Lung Cancer: A Systematic Review and Literature-Based Meta-Analysis.

Authors:  Alfredo Addeo; Giuseppe Luigi Banna; Giulio Metro; Massimo Di Maio
Journal:  Front Oncol       Date:  2019-04-16       Impact factor: 6.244

10.  Tislelizumab Plus Chemotherapy vs Chemotherapy Alone as First-line Treatment for Advanced Squamous Non-Small-Cell Lung Cancer: A Phase 3 Randomized Clinical Trial.

Authors:  Jie Wang; Shun Lu; Xinmin Yu; Yanping Hu; Yuping Sun; Zhijie Wang; Jun Zhao; Yan Yu; Chunhong Hu; Kunyu Yang; Guosheng Feng; Kejing Ying; Wu Zhuang; Jianying Zhou; Jingxun Wu; Shiang Jiin Leaw; Jing Zhang; Xiao Lin; Liang Liang; Nong Yang
Journal:  JAMA Oncol       Date:  2021-05-01       Impact factor: 31.777

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  1 in total

Review 1.  The effects of glucocorticoids and immunosuppressants on cancer outcomes in checkpoint inhibitor therapy.

Authors:  Sebastian Bruera; Maria E Suarez-Almazor
Journal:  Front Oncol       Date:  2022-08-23       Impact factor: 5.738

  1 in total

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