Association between pretreatment lymphocyte count and efficacy of immune-enhancing therapy in acute necrotising pancreatitis: a post-hoc analysis of the multicentre, randomised, placebo-controlled TRACE trial. (April 2023)
- Record Type:
- Journal Article
- Title:
- Association between pretreatment lymphocyte count and efficacy of immune-enhancing therapy in acute necrotising pancreatitis: a post-hoc analysis of the multicentre, randomised, placebo-controlled TRACE trial. (April 2023)
- Main Title:
- Association between pretreatment lymphocyte count and efficacy of immune-enhancing therapy in acute necrotising pancreatitis: a post-hoc analysis of the multicentre, randomised, placebo-controlled TRACE trial
- Authors:
- Ke, Lu
Mao, Wenjian
Shao, Fang
Zhou, Jing
Xu, Minyi
Chen, Tao
Liu, Yuxiu
Tong, Zhihui
Windsor, John
Ma, Penglin
Li, Weiqin
Ke, Lu
Mao, Wenjian
Zhou, Jing
Xu, Minyi
Jiang, Wendi
Zhang, He
Lin, Jiajia
Lu, Mengjie
Chen, Yan
Ma, Mingmin
Li, Gang
Ye, Bo
Li, Baiqiang
Tong, Zhihui
Liu, Yuxiu
Li, Weiqin
Shao, Fang
Chen, Tao
Lv, Nonghua
Zhu, Yin
Xia, Liang
He, Wenhua
Zhenping,
Chen,
Pan, Xinting
Zhu, Qingyun
Wan, Youdong
Mei, Hong
Li, Kang
Chen, Miao
He, Chengjian
Yao, Hongyi
Zhu, Zigui
Gu, Weili
Lu, Weihua
Wu, Jingyi
Zhou, Feng
Tu, Shumin
Fu, Long
Xue, Bingg
Ni, Haibin
Huang, Xiaofei
Zhou, Dandan
Zhang, Guoxiu
Ren, Lening
Li, Dahuan
Zhao, Xiangyang
Zhao, Wei
Chen, Xiaomei
Sun, Junli
Xin, Keke
Chen, Weiwei
Xu, Qingcheng
Song, Jingchun
Zeng, Qingbo
Shao, Min
Zhao, Dongsheng
Tu, Jianfeng
Yang, Honggup
… (more) - Abstract:
- Summary: Background: Immune-enhancing thymosin alpha 1 (Tα1) therapy may reduce infected pancreatic necrosis (IPN) in acute necrotising pancreatitis (ANP). However, the efficacy might be impacted by lymphocyte count due to the pharmacological action of Tα1. In this post-hoc analysis, we tested the hypothesis that pre-treatment absolute lymphocyte count (ALC) determines whether patients with ANP benefit from Tα1 therapy. Methods: A post-hoc analysis of data from a multicentre, double-blind, randomised, placebo-controlled trial testing the efficacy of Tα1 therapy in patients with predicted severe ANP was performed. Patients from 16 hospitals of China were randomised to receive a subcutaneous injection of Tα1 1.6 mg every 12 h for the frst 7 days and 1.6 mg once a day for the following 7 days or a matching placebo during the same period. Patients who discontinued the Tα1 regimen prematurely were excluded. Three subgroup analyses were conducted using the baseline ALC (at randomisation), and the group allocation was maintained as intention-to-treat. The primary outcome was the incidence of IPN 90 days after randomisation. The fitted logistic regression model was applied to identify the range of baseline ALC where Tα1 therapy could exert a maximum effect. The original trial is registered with ClinicalTrials.gov, NCT02473406 . Findings: Between March 18, 2017, and December 10, 2020, a total of 508 patients were randomised in the original trial, and 502 were involved in thisSummary: Background: Immune-enhancing thymosin alpha 1 (Tα1) therapy may reduce infected pancreatic necrosis (IPN) in acute necrotising pancreatitis (ANP). However, the efficacy might be impacted by lymphocyte count due to the pharmacological action of Tα1. In this post-hoc analysis, we tested the hypothesis that pre-treatment absolute lymphocyte count (ALC) determines whether patients with ANP benefit from Tα1 therapy. Methods: A post-hoc analysis of data from a multicentre, double-blind, randomised, placebo-controlled trial testing the efficacy of Tα1 therapy in patients with predicted severe ANP was performed. Patients from 16 hospitals of China were randomised to receive a subcutaneous injection of Tα1 1.6 mg every 12 h for the frst 7 days and 1.6 mg once a day for the following 7 days or a matching placebo during the same period. Patients who discontinued the Tα1 regimen prematurely were excluded. Three subgroup analyses were conducted using the baseline ALC (at randomisation), and the group allocation was maintained as intention-to-treat. The primary outcome was the incidence of IPN 90 days after randomisation. The fitted logistic regression model was applied to identify the range of baseline ALC where Tα1 therapy could exert a maximum effect. The original trial is registered with ClinicalTrials.gov, NCT02473406 . Findings: Between March 18, 2017, and December 10, 2020, a total of 508 patients were randomised in the original trial, and 502 were involved in this analysis, with 248 in the Tα1 group and 254 in the placebo group. Across the three subgroups, there was a uniform trend toward more significant treatment effects in patients with higher baseline ALC. Within the subgroup of patients with baseline ALC≥0.8 × 10ˆ9/L (n = 290), the Tα1 therapy significantly reduced the risk of IPN (covariate adjusted risk difference, −0.12; 95% CI, −0.21, -0.02; p = 0.015). Patients with baseline ALC between 0.79 and 2.00 × 10ˆ9/L benefited most from the Tα1 therapy in reducing IPN (n = 263). Interpretation: This post-hoc analysis found that the efficacy of immune-enhancing Tα1 therapy on the incidence of IPN may be associated with pretreatment lymphocyte count in patients with acute necrotising pancreatitis. Funding: National Natural Science Foundation of China . … (more)
- Is Part Of:
- EClinicalMedicine. Volume 58(2023)
- Journal:
- EClinicalMedicine
- Issue:
- Volume 58(2023)
- Issue Display:
- Volume 58, Issue 2023 (2023)
- Year:
- 2023
- Volume:
- 58
- Issue:
- 2023
- Issue Sort Value:
- 2023-0058-2023-0000
- Page Start:
- Page End:
- Publication Date:
- 2023-04
- Subjects:
- Acute pancreatitis -- Immunosuppression -- Thymosin -- Pancreatic necrosis -- Infection
Medicine -- Research -- Periodicals
Medical policy -- Periodicals
Clinical Medicine
Health Policy
Public Health
Medical policy
Medicine -- Research
Periodical
Electronic journals
Periodicals
613 - Journal URLs:
- https://www.sciencedirect.com/science/journal/25895370 ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.eclinm.2023.101915 ↗
- Languages:
- English
- ISSNs:
- 2589-5370
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- Legaldeposit
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