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Verification of the Prediction Accuracy of a Biomarker-Based Prognostic for Veno-Occlusive Disease/Sinusoidal Obstruction Syndrome (VOD/SOS) After Hematopoietic Cell Transplantation (HCT).
Putta, Santosh; Young, Bradford; Pine, Polly; Shi, Ju; Amber, Vian; Saber, Wael; Levine, John E; Grupp, Stephan A.
Afiliação
  • Putta S; BioLegend, San Diego, California. Electronic address: santosh.putta@biolegend.com.
  • Young B; B.A.Y. Biotech Consulting, Annapolis, Maryland.
  • Pine P; Jazz Pharmaceuticals, Palo Alto, California.
  • Shi J; Jazz Pharmaceuticals, Palo Alto, California.
  • Amber V; Jazz Pharmaceuticals, Oxford, UK.
  • Saber W; CIBMTR, Milwaukee, Wisconsin.
  • Levine JE; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Grupp SA; Pediatric Oncology, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Transplant Cell Ther ; 2024 Jul 10.
Article em En | MEDLINE | ID: mdl-38996974
ABSTRACT
Veno-occlusive disease/sinusoidal obstruction syndrome (VOD/SOS) is a potentially life-threatening complication of hematopoietic cell transplantation (HCT), especially in severe cases. Patient outcomes are improved with prompt treatment; however, diagnosing this disease is challenging as many clinical symptoms of VOD/SOS overlap with other post-HCT complications. A biomarker-based prognostic test for the assessment of VOD/SOS risk, termed "VODCheck" was developed in a previous study but has not yet been validated. This study aimed to validate the accuracy of VODCheck as a prognostic test for VOD/SOS in an independent cohort of patients. VODCheck incorporates hyaluronan (HA), angiopoietin-2 (ANG-2), and thrombomodulin (TM) based on their association with VOD/SOS, their analytical characteristics, and their ability to complement each other in a multivariate prognostic model. To validate VODCheck we measured plasma biomarker levels from a subset of patients enrolled in the control arm of a phase 3 study that tested VOD/SOS prophylaxis. We used a hierarchical design with prespecified primary (day 7), secondary A (day 15), and secondary B (day 1) hypotheses to verify the prognostic accuracy of VODCheck post-HCT. The cases of VOD/SOS (n = 22) were age-matched ∼13 with controls (n = 65). VODCheck was prognostic of VOD/SOS risk at all 3 time points with an area under the curve (AUC) of .815 (P < .001) for day 7, .836 (P < .001) for day 15, and .706 (P = .002) for day 1 post-HCT. A multivariate analysis confirmed the prognostic accuracy of VODCheck after adjustment for confounders such as age, VOD/SOS risk status, primary disease, and ozogamicin treatment. VODCheck was validated as an independent predictor of risk for VOD/SOS within 15 days post-HCT and appears to provide clinicians with actionable information to improve patient care.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Transplant Cell Ther Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Transplant Cell Ther Ano de publicação: 2024 Tipo de documento: Article