The evolution and impact of sarcopenia in severe aplastic anaemia survivors following allogeneic haematopoietic cell transplantation

Author:

Chen Dandan1,Yuan Zhaohu2,Guo Yuan1,Liu Weifeng3,Cheng Zixuan1,Ye Lihua1,Mo Wenjian4,Wei Xinhua1ORCID

Affiliation:

1. Department of Radiology, Guangzhou First People's Hospital, School of Medicine South China University of Technology Guangzhou China

2. Department of Blood Transfusion, Guangzhou First People's Hospital, School of Medicine South China University of Technology Guangzhou China

3. Guangzhou First People's Hospital, School of Medicine South China University of Technology Guangzhou China

4. Department of Hematology, Guangzhou First People's Hospital, School of Medicine South China University of Technology Guangzhou China

Abstract

AbstractBackgroundSarcopenia is a potential risk factor for adverse outcomes in haematopoietic cell transplantation (HSCT) recipients. We aimed to explore longitudinal body changes in muscle and adipose mass and their prognostic value in allogeneic HSCT‐treated severe aplastic anaemia (SAA) patients.MethodsWe retrospectively analysed consecutive SAA patients who underwent allogeneic HSCT between January 2017 and March 2022. Measurements of pectoral muscle and corresponding subcutaneous fat mass were obtained via chest computed tomography at baseline and at 1 month, 3 months, 6 months, and 12 months following HSCT. Sarcopenia was defined as pectoral muscle index (PMI) lower than the sex‐specific median at baseline. Changes in body composition over time were evaluated by generalized estimating equations. Cox regression models were used to investigate prognostic factors affecting overall survival (OS) and failure‐free survival (FFS). A nomogram was constructed from the Cox regression model for OS.ResultsWe included 298 adult SAA patients (including 129 females and 169 males) with a median age of 31 years [interquartile range (IQR), 24–39 years] at baseline. Sarcopenia was present in 148 (148/298, 50%) patients at baseline, 218 (218/285, 76%) patients post‐1 month, 209 (209/262, 80%) patients post‐3 month, 169 (169/218, 78%) patients post‐6 month, and 129 (129/181, 71%) patients post‐12 month. A significant decrease in pectoral muscle mass was observed in SAA patients from the time of transplant to 1 year after HSCT, and the greatest reduction occurred in post 1–3 months (P < 0.001). The sarcopenia group exhibited significantly lower 5‐year OS (90.6% vs. 100%, log‐rank P = 0.039) and 5‐year FFS (89.2% vs. 100%, log‐rank P = 0.021) than the nonsarcopenia group at baseline. Sarcopenia at baseline (hazard ratio, HR, 6.344; 95% confidence interval, CI: 1.570–25.538; P = 0.01; and HR, 3.275; 95% CI: 1.159–9.252; P = 0.025, respectively) and the delta value of the PMI at 6 months post‐transplantation (ΔPMI6) (HR, 0.531; 95% CI: 0.374–0.756; P < 0.001; and HR, 0.666; 95% CI: 0.505–0.879; P = 0.004, respectively) were demonstrated to be independent prognostic factors for OS and FFS in SAA patients undergoing HSCT, and were used to construct the nomogram. The C‐index of the nomogram was 0.75, and the calibration plot showed good agreement between the predictions made by the nomogram and actual observations.ConclusionsSarcopenia persists in SAA patients from the time of transplant to the 1‐year follow‐up after HSCT. Both sarcopenia at baseline and at 6 months following HSCT are associated with poor clinical outcomes, especially in patients with persistent muscle mass loss up to 6 months after transplantation.

Funder

Basic and Applied Basic Research Foundation of Guangdong Province

Publisher

Wiley

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