External validation and comparison of multiple prognostic scores in allogeneic hematopoietic stem cell transplantation

Roni Shouval, Joshua A. Fein, Aniela Shouval, Ivetta Danylesko, Noga Shem-Tov, Maya Zlotnik, Ronit Yerushalmi, Avichai Shimoni, Arnon Nagler

Research output: Contribution to journalArticlepeer-review

71 Scopus citations

Abstract

Clinical decisions in allogeneic hematopoietic stem cell transplantation (allo-HSCT) are supported by the use of prognostic scores for outcome prediction. Scores vary in their features and in the composition of development cohorts. We sought to externally validate and compare the performance of 8 commonly applied scoring systems on a cohort of allo-HSCT recipients. Among 528 patients studied, acute myeloid leukemia was the leading transplant indication (44%) and 46% of patients had a matched sibling donor. Most models successfully grouped patients into higher and lower risk strata, supporting their use for risk classification. However, discrimination varied (2-year overall survival area under the receiver operating characteristic curve [AUC]: revised Pretransplantation Assessment of Mortality [rPAM], 0.64; PAM, 0.63; revised Disease Risk Index [rDRI], 0.62; Endothelial Activation and Stress Index [EASIx], 0.60; combined European Society for Blood and Marrow Transplantation [EBMT]/Hematopoietic Cell Transplantation-specific Comorbidity Index [HCT-CI], 0.58; EBMT, 0.58; Comorbidity-Age, 0.58; HCT-CI, 0.55); AUC ranges from 0.5 (random) to 1.0 (perfect prediction). rPAM and PAM, which had the greatest predictive capacity across all outcomes, are comprehensive models including patient, disease, and transplantation information. Interestingly, EASIx, a biomarker-driven model, had comparable performance for nonrelapse mortality (NRM; 2-year AUC, 0.65) but no predictive value for relapse (2-year AUC, 0.53). Overall, allo-HSCT prognostic systems may be useful for risk stratification, but individual prediction remains a challenge, as reflected by the scores’ limited discriminative capacity.

Original languageEnglish
Pages (from-to)1881-1890
Number of pages10
JournalBlood advances
Volume3
Issue number12
DOIs
StatePublished - 25 Jun 2019
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2019 by The American Society of Hematology

Funding

This work was supported by The Varda and Boaz Dotan Research Center in Hemato-Oncology affiliated with the Cancer Biology Research Center of Tel Aviv University and The Shalvi Foundation for the Support of Medical Research.

FundersFunder number
Shalvi Foundation
Varda and Boaz Dotan Research Center
Tel Aviv University

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