The Composite Immune Risk Score predicts overall survival after allogeneic hematopoietic stem cell transplantation: A retrospective analysis of 1838 cases

Author:

Cao Yigeng12,Gong Xiaowen12,Feng Yahui12,Wang Mingyang12,Hu Yu12,Liu Huilan34,Liu Xueou12,Qi Saibing12,Ji Yanping56,Liu Fang12,Zhu Huaiping4,Guo Wenwen12,Shen Qiujin12,Zhang Rongli12,Zhao Ningning12,Zhai Weihua12,Song Xiaoqiang12,Chen Xin12,Geng Liangquan3,Chen Xia12,Zheng Xuetong12,Ma Qiaoling12,Tang Baolin3,Wei Jialin12,Huang Yong12,Ren Yuanyuan12,Song Kaidi3,Yang Donglin12,Pang Aiming12,Yao Wen3,He Yi12,Shang Yue12,Wan Xiang3,Zhang Wei12,Zhang Song12,Sun Guangyu3,Feng Sizhou12,Zhu Xiaofan12,Han Mingzhe12,Song Zhen12,Guo Ye12,Sun Zimin34,Jiang Erlie12ORCID,Chen Junren12ORCID

Affiliation:

1. State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital Chinese Academy of Medical Sciences & Peking Union Medical College Tianjin China

2. Tianjin Institutes of Health Science Tianjin China

3. Department of Hematology The First Affiliated Hospital of University of Science and Technology of China Hefei China

4. Blood and Cell Therapy Institute, Division of Life Sciences and Medicine, Anhui Provincial Key Laboratory of Blood Research and Applications University of Science and Technology of China Hefei China

5. Anhui Medical University Hefei China

6. Department of Hematology Affiliated Hospital of Jiangsu University Zhenjiang China

Abstract

AbstractThere has been little consensus on how to quantitatively assess immune reconstitution after hematopoietic stem cell transplantation (HSCT) as part of the standard of care. We retrospectively analyzed 11 150 post‐transplant immune profiles of 1945 patients who underwent HSCT between 2012 and 2020. 1838 (94.5%) of the cases were allogeneic HSCT. Using the training set of patients (n = 729), we identified a composite immune signature (integrating neutrophil, total lymphocyte, natural killer, total T, CD4+ T, and B cell counts in the peripheral blood) during days 91–180 after allogeneic HSCT that was predictive of early mortality and moreover simplified it into a formula for a Composite Immune Risk Score. When we verified the Composite Immune Risk Score in the validation (n = 284) and test (n = 391) sets of patients, a high score value was found to be associated with hazard ratios (HR) of 3.64 (95% C.I. 1.55–8.51; p = .0014) and 2.44 (95% C.I., 1.22–4.87; p = .0087), respectively, for early mortality. In multivariate analysis, a high Composite Immune Risk Score during days 91–180 remained an independent risk factor for early mortality after allogeneic HSCT (HR, 1.80; 95% C.I., 1.28–2.55; p = .00085). In conclusion, the Composite Immune Risk Score is easy to compute and could identify the high‐risk patients of allogeneic HSCT who require targeted effort for prevention and control of infection.

Funder

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

State Key Laboratory of Experimental Hematology

Publisher

Wiley

Subject

Hematology

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