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Assessment of ST2 for Risk of Death Following Graft-versus-Host Disease in the Pediatric and Adult Age Groups

41 Pages Posted: 28 Jun 2019

See all articles by Courtney Rowan

Courtney Rowan

Indiana University - School of Medicine

Francis Pike

Indiana University - School of Medicine

Kenneth R. Cooke

Johns Hopkins University - School of Medicine

Robert Krance

Baylor University - Texas Children's Hospital

Paul A. Carpenter

Fred Hutchinson Cancer Research Center

Christine Duncan

Harvard University - Boston Children’s Hospital

David A. Jacobsohn

George Washington University - Children's National Medical Center

Catherine M. Bollard

Children's National Medical Center; George Washington University - Department of Microbiology, Immunology and Tropical Medicine

Russell Cruz

Children’s National Medical Center

Abhijeet Malatpure

Indiana University - School of Medicine

Sherif S. Farag

Indiana University - School of Medicine

Jamie Renbarger

Indiana University - School of Medicine

Hao Liu

Indiana University - School of Medicine

Giorgos Bakoyannis

Indiana University - School of Medicine

Samir Hanash

University of Texas at Houston - MD Anderson Cancer Center

Sophie Paczesny

Indiana University - Department of Pediatrics; Indiana University - Department of Microbiology and Immunology

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Abstract

Background: To address the need for establishing prognostic markers of Non-Relapse Mortality (NRM) and acute graft-versus-hostdisease (aGVHD) after allogeneic hematopoietic cell transplantation (HCT) in the pediatric age group, we conducted a prospective study (NCT02194439).

Methods: 415 patients at six U.S. centers including 170 children ≤10 years were accrued from 2013 to 2018. Four biomarkers [stimulation-2 (ST2), interleukin-6, regenerating-islet-derived-3-alpha (REG3α) and tumornecrosis-factor-receptor-1 (TNFR1)] were assessed in the plasma pre-HCT (day -7), and at days +7, +14, +21 post-HCT. We performed landmark analyses for NRM and grade II-IV aGVHD, dichotomizing the cohort at ≤10 years and using each biomarker median as a cutoff for high and low risk groups. The multivariable analyses included the significant covariates.

Findings: The NRM was not different among children ≤10 years compared to subjects >10 years. Landmark analyses using post-HCT assays showed that ST2 (>26 ng/mL), TNFR1 (>3441 pg/mL), and REG3α (>25 ng/mL) are associated with NRM in both children <10 years [Hazard Ratio (HR) Confidence Intervals (CI): ST2: 9.13 (2.74-30.38), p=0.0003; TNFR1: 4.29 (1.48-12.48), p=0.0073; REG3α: 7.28 (2.05-25.93), p=0.0022] and children/adults >10 years [HR (CI): ST2: 2.60 (1.15-5.86), p=0.021; TNFR1: 2.09 (0.96-4.58), p=0.06; REG3α: 2.57 (1.19-5.55), p=0.016]. When pre-HCT biomarkers were included, ST2 remained significant in both cohorts. After adjustment for significant covariates (race/ethnicity, malignant disease, graft, GVHD prophylaxis), ST2 remained associated with NRM only in recipients ≤10 years [HR(CI): 4.82 (1.89-14.66), p=0.0056]. ST2 was also associated with grade II-IV aGVHD in both ≤10 years and >10 years groups (p=0.0059, and p<0.0001).

Interpretation: Assays of ST2, TNFR1, REG3α in the first 3 weeks following HCT have prognostic value for NRM and aGVHD in both children and adults. ST2 prior to HCT is a prognostic biomarker for NRM and severe aGVHD in children ≤10 years allowing for additional stratification.

Trial Registration: Clinicaltrial.gov under NCT02194439.

Funding Statement: The Eunice Kennedy Shriver National Institute of Child Health and Human Development of Health from the National Institutes of Health R01HD074587, the National Cancer Institute R01CA168814, the Leukemia and Lymphoma Society (grant 1293-15), and the Lilly Physician Scientist Initiative Award.

Declaration of Interests: S.P. is an inventor on a patent on “Methods of detection of graft-versus-host disease” (US- 13/573,766). K.R.C. is on the advisory board of Jazz pharmaceuticals. All other authors declare no competing interests.

Ethics Approval Statement: This study was approved by the respective Institutional Review Boards at six adult and pediatric centers: Children's National Medical Center, Texas Children's Hospital, Fred Hutchinson Cancer Research Center, Boston Children’s/Dana Farber Cancer Institute, Johns Hopkins, and Indiana University. Informed consent was obtained from all patients or their legal guardians.

Keywords: biomarkers, graft-versus-host-disease, allogeneic hematopoietic cell transplantation, pediatric

Suggested Citation

Rowan, Courtney and Pike, Francis and Cooke, Kenneth R. and Krance, Robert and Carpenter, Paul A. and Duncan, Christine and Jacobsohn, David A. and Bollard, Catherine M. and Cruz, Russell and Malatpure, Abhijeet and Farag, Sherif S. and Renbarger, Jamie and Liu, Hao and Bakoyannis, Giorgos and Hanash, Samir and Paczesny, Sophie, Assessment of ST2 for Risk of Death Following Graft-versus-Host Disease in the Pediatric and Adult Age Groups (June 24, 2019). Available at SSRN: https://ssrn.com/abstract=3409311 or http://dx.doi.org/10.2139/ssrn.3409311

Courtney Rowan

Indiana University - School of Medicine ( email )

340 W 10th St #6200
Indianapolis, IN 46202
United States

Francis Pike

Indiana University - School of Medicine

340 W 10th St #6200
Indianapolis, IN 46202
United States

Kenneth R. Cooke

Johns Hopkins University - School of Medicine

733 North Broadway
Suite G-49
Baltimore, MD 21205-2196
United States

Robert Krance

Baylor University - Texas Children's Hospital

6621 Fannin St
Houston, TX 77030
United States

Paul A. Carpenter

Fred Hutchinson Cancer Research Center

1100 Fairview Avenue North
M2-C206
Seattle, WA 98109-1024
United States

Christine Duncan

Harvard University - Boston Children’s Hospital

300 Longwood Avenue
Landmark 5th Floor East
Boston, MA 02115
United States

David A. Jacobsohn

George Washington University - Children's National Medical Center

DC
United States

Catherine M. Bollard

Children's National Medical Center

DC
United States

George Washington University - Department of Microbiology, Immunology and Tropical Medicine

Washington, DC
United States

Russell Cruz

Children’s National Medical Center

111 Michigan Ave. NW
Washington, DC
United States

Abhijeet Malatpure

Indiana University - School of Medicine

340 W 10th St #6200
Indianapolis, IN 46202
United States

Sherif S. Farag

Indiana University - School of Medicine

340 W 10th St #6200
Indianapolis, IN 46202
United States

Jamie Renbarger

Indiana University - School of Medicine

340 W 10th St #6200
Indianapolis, IN 46202
United States

Hao Liu

Indiana University - School of Medicine

340 W 10th St #6200
Indianapolis, IN 46202
United States

Giorgos Bakoyannis

Indiana University - School of Medicine

340 W 10th St #6200
Indianapolis, IN 46202
United States

Samir Hanash

University of Texas at Houston - MD Anderson Cancer Center

1901 East Road, Unit 1950
Unit 1905
Houston, TX 77030
United States

Sophie Paczesny (Contact Author)

Indiana University - Department of Pediatrics ( email )

705 Riley Hospital Dr.
Indianapolis, IN 46202
United States

Indiana University - Department of Microbiology and Immunology ( email )

635 Barnhill Drive
Medical Science 420
Indianapolis, IN 46202
United States

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