Chronic GvHD NIH Consensus Project Biology Task Force: Evolving path to personalized treatment of chronic GvHD

Author:

Buxbaum Nataliya Prokopenko1,Socié Gerard2,Hill Geoffrey R3,MacDonald Kelli PA4,Tkachev Victor5ORCID,Teshima Takanori6ORCID,Lee Stephanie J7ORCID,Ritz Jerome8ORCID,Sarantopoulos Stefanie9,Luznik Leo10,Zeng Defu11ORCID,Paczesny Sophie12ORCID,Martin Paul J.3ORCID,Pavletic Steven Z13,Schultz Kirk R14,Blazar Bruce R.15ORCID

Affiliation:

1. Roswell Park Comprehensive Cancer Center, Buffalo, New York, United States

2. Division of Hematology, Hospital Saint Louis & University Paris, Paris, France, Paris, France

3. Fred Hutchinson Cancer Research Center, Seattle, Washington, United States

4. QIMR Berghofer MRI, Brisbane, Australia

5. Boston Children's Hospital, Boston, Massachusetts, United States

6. Hokkaido University Faculty of Medicine, Sapporo, Japan

7. Fred Hutchinson Cancer Center, Seattle, Washington, United States

8. Dana-Farber Cancer Institute; Harvard Medical School, Boston, Massachusetts, United States

9. Duke University, Durham, North Carolina, United States

10. Johns Hopkins University, Baltimore, Maryland, United States

11. The Beckman Research Institute of City of Hope, Duarte,, California, United States

12. Medical University of South Carolina, Charleston, South Carolina, United States

13. National Cancer Institute, Bethesda, Maryland, United States

14. BC Children's Hospital, Vancouver, Canada

15. University of Minnesota, Minneapolis, Minnesota, United States

Abstract

Chronic GvHD (cGvHD) remains a prominent barrier to allogeneic hematopoietic stem cell transplantion as the leading cause of non-relapse mortality and significant morbidity. Tremendous progress has been achieved in both understanding of pathophysiology and the development of new therapies for cGvHD. While our field has historically approached treatment from an empiric position, research performed at the bedside and bench has elucidated some of the complex pathophysiology of cGvHD. From the clinical perspective, there is significant variability of disease manifestations between individual patients, pointing to diverse biological underpinnings. Capitalizing on progress made to date, the field is now focused on establishing personalized treatment approaches. The manuscript's intent is to concisely review recent knowledge gained and formulate a path towards patient-specific cGvHD therapy.

Publisher

American Society of Hematology

Subject

Hematology

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