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National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: IIb. The 2020 Preemptive Therapy Working Group Report.
Pidala, Joseph; Kitko, Carrie; Lee, Stephanie J; Carpenter, Paul; Cuvelier, Geoffrey D E; Holtan, Shernan; Flowers, Mary E; Cutler, Corey; Jagasia, Madan; Gooley, Ted; Palmer, Joycelynne; Randolph, Tim; Levine, John E; Ayuk, Francis; Dignan, Fiona; Schoemans, Helene; Tkaczyk, Eric; Farhadfar, Nosha; Lawitschka, Anita; Schultz, Kirk R; Martin, Paul J; Sarantopoulos, Stefanie; Inamoto, Yoshihiro; Socie, Gerard; Wolff, Daniel; Blazar, Bruce; Greinix, Hildegard; Paczesny, Sophie; Pavletic, Steven; Hill, Geoffrey.
Afiliação
  • Pidala J; Blood and Marrow Transplantation and Cellular Immunotherapy, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida. Electronic address: joseph.pidala@moffitt.org.
  • Kitko C; Division of Pediatric Hematology/Oncology, Dpeartment of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Lee SJ; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Carpenter P; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Cuvelier GDE; Cancer Care Manitoba, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Holtan S; Division of Hematology, Oncology, and Transplantation, Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota.
  • Flowers ME; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Cutler C; Division of Stem Cell Transplantation and Cellular Therapy, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Jagasia M; Division of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Gooley T; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Palmer J; Division of Biostatistics, Department of Computational and Quantitative Medicine, City of Hope, Duarte, California.
  • Randolph T; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Levine JE; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Ayuk F; Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Dignan F; Department of Clinical Haematology, Manchester Royal Infirmary, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
  • Schoemans H; Department of Hematology, University Hospitals Leuven and Department of Public Health, KU Leuven, Leuven, Belgium.
  • Tkaczyk E; Department of Veterans Affairs and Departments of Dermatology and Biomedical Engineering, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Farhadfar N; Division of Hematology and Oncology, Department of Medicine, University of Florida, Gainesville, Florida.
  • Lawitschka A; Stem Cell Transplantation Unit, St Anna Children's Hospital, Medical University of Vienna, Vienna, Austria; Children's Cancer Research Institute, Vienna, Austria.
  • Schultz KR; Pediatric Hematology/Oncology/BMT, BC Children's Hospital, Vancouver, British Columbia, Canada.
  • Martin PJ; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Sarantopoulos S; Division of Hematological Malignancies and Cellular Therapy, Duke Cancer Institute, Duke University Department of Medicine, Durham, North Carolina.
  • Inamoto Y; Department of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
  • Socie G; Hematology and Bone Marrow Transplant Department, AP-HP Saint Louis Hospital and University of Paris, Paris, France.
  • Wolff D; Department of Internal Medicine III, University Hospital of Regensburg, Regensburg, Germany.
  • Blazar B; Department of Pediatrics, Division of Blood & Marrow Transplantation & Cellular Therapy, University of Minnesota, Minneapolis, Minnesota.
  • Greinix H; Clinical Division of Hematology, Medical University of Graz, Graz, Austria.
  • Paczesny S; Department of Microbiology and Immunology and Department of Pediatrics, Medical University of South Carolina, Charleston, South Carolina.
  • Pavletic S; Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Hill G; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Transplant Cell Ther ; 27(8): 632-641, 2021 08.
Article em En | MEDLINE | ID: mdl-33836313
ABSTRACT
Chronic graft-versus-host disease (GVHD) commonly occurs after allogeneic hematopoietic cell transplantation (HCT) despite standard prophylactic immune suppression. Intensified universal prophylaxis approaches are effective but risk possible overtreatment and may interfere with the graft-versus-malignancy immune response. Here we summarize conceptual and practical considerations regarding preemptive therapy of chronic GVHD, namely interventions applied after HCT based on evidence that the risk of developing chronic GVHD is higher than previously appreciated. This risk may be anticipated by clinical factors or risk assignment biomarkers or may be indicated by early signs and symptoms of chronic GVHD that do not fully meet National Institutes of Health diagnostic criteria. However, truly preemptive, individualized, and targeted chronic GVHD therapies currently do not exist. In this report, we (1) review current knowledge regarding clinical risk factors for chronic GVHD, (2) review what is known about chronic GVHD risk assignment biomarkers, (3) examine how chronic GVHD pathogenesis intersects with available targeted therapeutic agents, and (4) summarize considerations for preemptive therapy for chronic GVHD, emphasizing trial development, including trial design and statistical considerations. We conclude that robust risk assignment models that accurately predict chronic GVHD after HCT and early-phase preemptive therapy trials represent the most urgent priorities for advancing this novel area of research.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: America do norte Idioma: En Revista: Transplant Cell Ther Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: America do norte Idioma: En Revista: Transplant Cell Ther Ano de publicação: 2021 Tipo de documento: Article