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The lung allocation score and other available models lack predictive accuracy for post-lung transplant survival.
- Source :
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The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation [J Heart Lung Transplant] 2022 Aug; Vol. 41 (8), pp. 1063-1074. Date of Electronic Publication: 2022 May 20. - Publication Year :
- 2022
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Abstract
- Background: Improved predictive models are needed in lung transplantation in the setting of a proposed allocation system that incorporates longer-term post-transplant survival in the United States. Allocation systems require accurate mortality predictions to justly allocate organs.<br />Methods: Utilizing the United Network for Organ Sharing database (2005-2017), we fit models to predict 1-year mortality based on the Lung Allocation Score (LAS), the Chan, et al, 2019 model, a novel "clinician" model (a priori clinician selection of pre-transplant covariates), and two machine learning models (Least Absolute Shrinkage and Selection Operator; LASSO and Random Forests) for predicting 1-year and 3-year post-transplant mortality. We compared predictive accuracy among models. We evaluated the calibration of models by comparing average predicted probability vs observed outcome per decile. We repeated analyses fit for 3-year mortality, disease category, including donor covariates, and LAS era.<br />Results: The area under the cure for all models was low, ranging from 0.55 to 0.62. All exhibited reasonable negative predictive values (0.87-0.90), but the positive predictive value for was poor (all <0.25). Evaluating LAS calibration found 1-year post-transplant estimates consistently overestimated risk of mortality, with greater differences in higher deciles. LASSO, Random Forests, and clinician models showed no improvement when evaluated by disease category or with the addition of donor covariates and performed worse for 3-year outcomes.<br />Conclusions: The LAS overestimated patients' risk of post-transplant death, thus underestimating transplant benefit in the sickest candidates. Novel models based on pre-transplant recipient covariates failed to improve prediction. There should be wariness in post-transplant survival predictions from available models.<br />Competing Interests: Disclosure statement CHG, EDL, CAM, and KJR report additional grant support from the United States CFF. CAM reports grant support from the NIH Lung Transplant Outcomes Group. CHG reports grant support from the European Commission and NIH National Heart, Lung, and Blood Institute; National Institute of Diabetes and Digestive and Kidney Diseases; and National Center for Research Resources. CHG reports personal or other fees from Gilead Sciences, Novartis, Boehringer Ingelheim, and Vertex Pharmaceuticals. KJR reports grant support from the NIH. None of these financial relationships influenced the interpretation or reporting of the current study. Grant/Research Support; Current/Ongoing - CHEST Foundation Grant in CF in partnership with Vertex Pharmaceuticals, Cystic Fibrosis Foundation (CFF), and the National Institutes of Health (NIH) (K23HL138154). A portion of the findings were presented during the 2022 ISHLT 42nd Annual Meeting and Scientific Sessions as a Mini Oral presentation by JMB.<br /> (Copyright © 2022 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.)
Details
- Language :
- English
- ISSN :
- 1557-3117
- Volume :
- 41
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation
- Publication Type :
- Academic Journal
- Accession number :
- 35690561
- Full Text :
- https://doi.org/10.1016/j.healun.2022.05.008