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Weighted pseudo-values for partly unobserved group membership in paediatric stem cell transplantation studies

Generalised pseudo-values have been suggested to evaluate the impact of allogeneic stem cell transplantation on childhood leukaemia. The approach compares long-term survival of two cohorts defined by the availability or non-availability of suitable donors for stem cell transplantation. A patient...

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Autores principales: Mittlböck, Martina, Pötschger, Ulrike, Heinzl, Harald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8721556/
https://www.ncbi.nlm.nih.gov/pubmed/34812663
http://dx.doi.org/10.1177/09622802211041756
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author Mittlböck, Martina
Pötschger, Ulrike
Heinzl, Harald
author_facet Mittlböck, Martina
Pötschger, Ulrike
Heinzl, Harald
author_sort Mittlböck, Martina
collection PubMed
description Generalised pseudo-values have been suggested to evaluate the impact of allogeneic stem cell transplantation on childhood leukaemia. The approach compares long-term survival of two cohorts defined by the availability or non-availability of suitable donors for stem cell transplantation. A patient's cohort membership becomes known only after completed donor search with or without an identified donor. If a patient suffers an event during donor search, stem cell transplantation will no longer be indicated. In such a case, donor search will be ceased and cohort membership will remain unknown. The generalised pseudo-values approach considers donor identification as binary time-dependent covariate and uses inverse-probability-of-censoring weighting to adjust for non-identified donors. The approach leads to time-consuming computations due to multiple redefinitions of the risk set for pseudo-value calculation and an explicit adjustment for waiting-time bias. Here, the problem is looked at from a different angle. By considering the probability that a donor would have been identified after ceasing of donor search, weights for common pseudo-values are defined. This leads to a faster alternative approach as only a single risk set is necessary. Extensive computer simulations show that both, the generalised and the new weighted pseudo-values approach, provide approximately unbiased estimates. Confidence interval coverage is satisfactory for typical clinical scenarios. In situations, where donor identification takes considerably longer than usual, the weighted pseudo-values approach is preferable. Both approaches complement each other as they have different potential in addressing further aspects of the underlying medical question.
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spelling pubmed-87215562022-01-04 Weighted pseudo-values for partly unobserved group membership in paediatric stem cell transplantation studies Mittlböck, Martina Pötschger, Ulrike Heinzl, Harald Stat Methods Med Res Articles Generalised pseudo-values have been suggested to evaluate the impact of allogeneic stem cell transplantation on childhood leukaemia. The approach compares long-term survival of two cohorts defined by the availability or non-availability of suitable donors for stem cell transplantation. A patient's cohort membership becomes known only after completed donor search with or without an identified donor. If a patient suffers an event during donor search, stem cell transplantation will no longer be indicated. In such a case, donor search will be ceased and cohort membership will remain unknown. The generalised pseudo-values approach considers donor identification as binary time-dependent covariate and uses inverse-probability-of-censoring weighting to adjust for non-identified donors. The approach leads to time-consuming computations due to multiple redefinitions of the risk set for pseudo-value calculation and an explicit adjustment for waiting-time bias. Here, the problem is looked at from a different angle. By considering the probability that a donor would have been identified after ceasing of donor search, weights for common pseudo-values are defined. This leads to a faster alternative approach as only a single risk set is necessary. Extensive computer simulations show that both, the generalised and the new weighted pseudo-values approach, provide approximately unbiased estimates. Confidence interval coverage is satisfactory for typical clinical scenarios. In situations, where donor identification takes considerably longer than usual, the weighted pseudo-values approach is preferable. Both approaches complement each other as they have different potential in addressing further aspects of the underlying medical question. SAGE Publications 2021-11-23 2022-01 /pmc/articles/PMC8721556/ /pubmed/34812663 http://dx.doi.org/10.1177/09622802211041756 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Articles
Mittlböck, Martina
Pötschger, Ulrike
Heinzl, Harald
Weighted pseudo-values for partly unobserved group membership in paediatric stem cell transplantation studies
title Weighted pseudo-values for partly unobserved group membership in paediatric stem cell transplantation studies
title_full Weighted pseudo-values for partly unobserved group membership in paediatric stem cell transplantation studies
title_fullStr Weighted pseudo-values for partly unobserved group membership in paediatric stem cell transplantation studies
title_full_unstemmed Weighted pseudo-values for partly unobserved group membership in paediatric stem cell transplantation studies
title_short Weighted pseudo-values for partly unobserved group membership in paediatric stem cell transplantation studies
title_sort weighted pseudo-values for partly unobserved group membership in paediatric stem cell transplantation studies
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8721556/
https://www.ncbi.nlm.nih.gov/pubmed/34812663
http://dx.doi.org/10.1177/09622802211041756
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