Children's Oncology Group's 2023 blueprint for research: Cellular therapy and stem cell transplantation

Author:

Kitko Carrie L.1ORCID,Bollard Catherine M.234,Cairo Mitchell S.5ORCID,Chewning Joseph6,Fry Terry J.78,Pulsipher Michael A.9,Shenoy Shalini10,Wall Donna A.11,Levine John E.12ORCID

Affiliation:

1. Pediatric Stem Cell Transplant Program Vanderbilt University Medical Center Nashville Tennessee USA

2. Center for Cancer and Immunology Research Children's National Hospital Washington District of Columbia USA

3. GW Cancer Center George Washington University Washington District of Columbia USA

4. Division of Blood and Marrow Transplantation Children's National Hospital Washington District of Columbia USA

5. Division of Pediatric Hematology, Oncology and Stem Cell Transplantation, Maria Fareri Children's Hospital, Westchester Medical Center New York Medical College Valhalla New York USA

6. Division of Hematology and Oncology University of Alabama at Birmingham Birmingham Alabama USA

7. Department of Pediatrics University of Colorado Anschutz Medical Campus Aurora Colorado USA

8. Center for Cancer and Blood Disorders Children's Hospital Colorado Aurora Colorado USA

9. Division of Hematology and Oncology, Intermountain Primary Children's Hospital Huntsman Cancer Institute, Spencer Fox Eccles School of Medicine Salt Lake City Utah USA

10. Division of Pediatric Hematology and Oncology, Department of Pediatrics Washington University St Louis Missouri USA

11. Division of Haematology/Oncology Hospital for Sick Children Toronto Canada

12. Tisch Cancer Institute Icahn School of Medicine at Mount Sinai New York New York USA

Abstract

AbstractSince the publication of the last Cellular Therapy and Stem Cell Transplant blueprint in 2013, Children's Oncology Group cellular therapy‐based trials advanced the field and created new standards of care across a wide spectrum of pediatric cancer diagnoses. Key findings include that tandem autologous transplant improved survival for patients with neuroblastoma and atypical teratoid/rhabdoid brain tumors, one umbilical cord blood (UCB) donor was safer than two UCB donors, killer immunoglobulin receptor (KIR) mismatched donors did not improve survival for pediatric acute myeloid leukemia when in vivo T‐cell depletion is used, and the depth of remission as measured by next‐generation sequencing‐based minimal residual disease assessment pretransplant was the best predictor of relapse for acute lymphoblastic leukemia. Plans for the next decade include optimizing donor selection for transplants for acute leukemia/myelodysplastic syndrome, using novel engineered cellular therapies to target a wide array of malignancies, and developing better treatments for cellular therapy toxicities such as viral infections and graft‐vs‐host disease.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

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