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Phase 2 study of natalizumab plus standard corticosteroid treatment for high-risk acute graft-versus-host disease.
Al Malki, Monzr M; London, Kaitlyn; Baez, Janna; Akahoshi, Yu; Hogan, William J; Etra, Aaron; Choe, Hannah; Hexner, Elizabeth; Langston, Amelia; Abhyankar, Sunil; Ponce, Doris M; DeFilipp, Zachariah; Kitko, Carrie L; Adekola, Kehinde; Reshef, Ran; Ayuk, Francis; Capellini, Alexandra; Chanswangphuwana, Chantiya; Eder, Matthias; Eng, Gilbert; Gandhi, Isha; Grupp, Stephan; Gleich, Sigrun; Holler, Ernst; Javorniczky, Nora Rebeka; Kasikis, Stelios; Kowalyk, Steven; Morales, George; Özbek, Umut; Rösler, Wolf; Spyrou, Nikolaos; Yanik, Gregory; Young, Rachel; Chen, Yi-Bin; Nakamura, Ryotaro; Ferrara, James L M; Levine, John E.
Afiliação
  • Al Malki MM; Hematology/Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA.
  • London K; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Baez J; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Akahoshi Y; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Hogan WJ; Division of Hematology, Mayo Clinic, Rochester, MN.
  • Etra A; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Choe H; Division of Hematology, James Cancer Center, The Ohio State University, Columbus, OH.
  • Hexner E; Blood and Marrow Transplantation Program, Abramson Cancer Center, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
  • Langston A; Winship Cancer Institute, Emory University, Atlanta, GA.
  • Abhyankar S; Division of Hematologic Malignancies and Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS.
  • Ponce DM; Division of Hematology/Oncology, Department of Medicine, Adult Bone Marrow Transplantation Service, Memorial Sloan Kettering, New York, NY.
  • DeFilipp Z; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Kitko CL; Pediatric Stem Cell Transplant Program, Vanderbilt University Medical Center, Nashville, TN.
  • Adekola K; Division of Hematology/Oncology, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL.
  • Reshef R; Blood and Marrow Transplantation, Columbia University Medical Center, New York, NY.
  • Ayuk F; Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Capellini A; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Chanswangphuwana C; Department of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
  • Eder M; Department of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
  • Eng G; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Gandhi I; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Grupp S; Division of Oncology, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Gleich S; Department of Hematology and Oncology, Internal Medicine III, University of Regensburg, Regensburg, Germany.
  • Holler E; Department of Hematology and Oncology, Internal Medicine III, University of Regensburg, Regensburg, Germany.
  • Javorniczky NR; Department of Medicine I, Medical Center - University of Freiburg, Faculty of Medicine, Albert Ludwigs University, Freiburg, Germany.
  • Kasikis S; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Kowalyk S; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Morales G; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Özbek U; Department of Population Health Science and Policy, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Rösler W; Department of Internal Medicine 5, University Hospital Erlangen, Erlangen, Germany.
  • Spyrou N; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Yanik G; Blood and Marrow Transplant Program, Michigan Medicine, Ann Arbor, MI.
  • Young R; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Chen YB; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Nakamura R; Hematology/Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA.
  • Ferrara JLM; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Levine JE; The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Blood Adv ; 7(17): 5189-5198, 2023 09 12.
Article em En | MEDLINE | ID: mdl-37235690
ABSTRACT
Graft-versus-host disease (GVHD) of the gastrointestinal (GI) tract is the main cause of nonrelapse mortality (NRM) after allogeneic hematopoietic cell transplantation. Ann Arbor (AA) scores derived from serum biomarkers at onset of GVHD quantify GI crypt damage; AA2/3 scores correlate with resistance to treatment and higher NRM. We conducted a multicenter, phase 2 study using natalizumab, a humanized monoclonal antibody that blocks T-cell trafficking to the GI tract through the α4 subunit of α4ß7 integrin, combined with corticosteroids as primary treatment for patients with new onset AA2/3 GVHD. Seventy-five patients who were evaluable were enrolled and treated; 81% received natalizumab within 2 days of starting corticosteroids. Therapy was well tolerated with no treatment emergent adverse events in >10% of patients. Outcomes for patients treated with natalizumab plus corticosteroids were compared with 150 well-matched controls from the MAGIC database whose primary treatment was corticosteroids alone. There were no significant differences in overall or complete response between patients treated with natalizumab plus corticosteroids and those treated with corticosteroids alone (60% vs 58%; P = .67% and 48% vs 48%; P = 1.0, respectively) including relevant subgroups. There were also no significant differences in NRM or overall survival at 12 months in patients treated with natalizumab plus corticosteroids compared with controls treated with corticosteroids alone (38% vs 39%; P = .80% and 46% vs 54%; P = .48, respectively). In this multicenter biomarker-based phase 2 study, natalizumab combined with corticosteroids failed to improve outcome of patients with newly diagnosed high-risk GVHD. This trial was registered at www.clinicaltrials.gov as # NCT02133924.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article