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Published on: May 7, 2015
Elevation of Urinary Liver-Type Fatty Acid-Binding Protein Is a Harbinger of Poor Patient Prognosis after Allogeneic
Naoki Shingai1, Akihito Ota2, Kana Kato1
1Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Bunkyo-ku, Tokyo, Japan.
Insights
Elevated urinary liver-type fatty acid-binding protein (uL-FABP) before stem cell transplantation (SCT) predicts poor overall survival and nonrelapse mortality. Baseline uL-FABP measurement offers a simple method for predicting SCT patient survival.
Area of Science:
- Nephrology
- Oncology
- Biomarkers
Background:
- Urinary liver-type fatty acid-binding protein (uL-FABP) is a prognostic biomarker for various diseases.
- Previous studies indicated uL-FABP may predict acute kidney injury post-stem cell transplantation (SCT).
- The prognostic value of uL-FABP for overall survival in SCT patients remained undetermined.
Purpose of the Study:
- To investigate if uL-FABP levels can stratify patient prognosis after SCT.
- To determine the association between baseline and post-SCT uL-FABP levels and survival outcomes.
Main Methods:
- A long-term follow-up study of patients from a preceding prospective cohort.
- Classification into high and low uL-FABP groups based on pre-conditioning baseline levels (cutoff 8.4 μg/gCr).
- Cox proportional hazard and Fine-Gray regression models were used for survival and competing risk analyses, respectively.
Main Results:
- High baseline uL-FABP was a significant predictor of poor 5-year overall survival (HR 3.54, P=.002).
- High baseline uL-FABP was also a significant predictor of 5-year nonrelapse mortality (HR 3.37, P=.01).
- Post-SCT uL-FABP levels (days 0, 7, 14) did not significantly predict survival outcomes.
Conclusions:
- Pre-conditioning baseline uL-FABP is a significant prognostic factor for overall survival and nonrelapse mortality in SCT patients.
- Measuring baseline uL-FABP provides a simple and effective method for predicting survival in patients undergoing SCT.
- Post-transplant uL-FABP levels do not appear to be significant predictors of survival.
Abstract:
Several recent studies have demonstrated that urinary levels of liver-type fatty acid-binding protein (L-FABP) can be used to stratify the prognosis of cardiac disease, cardiac intensive care unit admission, cirrhosis, and coronavirus disease 2019. Our initial prospective study revealed that urinary L-FABP (uL-FABP) was associated with a high probability of acute kidney injury after stem cell transplantation (SCT); however, the relevance of elevated uL-FABP to the prognosis of patients undergoing SCT remains to be determined. We aimed to investigate whether uL-FABP levels can be used to stratify patient prognosis after SCT. To achieve this aim, we conducted a new long-term follow-up study using data from patients enrolled in our preceding prospective cohort study. Patients were classified into high and low uL-FABP groups based on levels measured at baseline (ie, before initiating the conditioning regimen), using an uL-FABP cutoff of 8.4 μg/gCr, which was determined based on data from healthy adults. uL-FABP levels were also measured on days 0, 7, and 14 after SCT. Cox proportional hazard regression was used to examine the effects of each factor on survival outcomes, and Fine-Gray regression was used in the presence of competing risks. Multivariate analysis incorporating confounders was then performed for factors with P < .1 in univariate analysis. In total, 20 of 84 patients (23.8%), 57 of 84 patients (67.9%), 34 of 49 patients (69.4%), and 34 of 46 patients (73.9%) were classified into the high uL-FABP group at baseline and on days 0, 7, and 14, respectively. The 5-year overall survival (OS) rate was 23.9% in the high uL-FABP group and 68.9% in the low uL-FABP group. The multivariate analysis identified a high uL-FABP level at baseline as a significant prognostic factor for poor OS (hazard ratio [HR], 3.54; P = .002). The 5-year cumulative incidence rate for nonrelapse mortality (NRM) was 50.0% in the high uL-FABP group and 19.9% in the low uL-FABP group. In the multivariate analysis, high uL-FABP at baseline was a significant prognostic factor for NRM (HR, 3.37; P = .01). uL-FABP levels did not significantly stratify the cumulative incidence of relapse (HR, 2.13; P = .11). uL-FABP levels on days 0, 7, and 14 were not significant predictors of survival. High uL-FABP level before initiation of conditioning significantly influences OS and NRM following SCT, whereas a high uL-FABP level at any point after the conditioning regimen does not. Our results show that measuring uL-FABP level at baseline may be a simple way to predict survival in patients undergoing SCT.
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