Phase 2 study of natalizumab plus standard corticosteroid treatment for high-risk acute graft-versus-host disease

Author:

Al Malki Monzr M.1ORCID,London Kaitlyn2,Baez Janna2,Akahoshi Yu2ORCID,Hogan William J.3ORCID,Etra Aaron2,Choe Hannah4,Hexner Elizabeth5ORCID,Langston Amelia6ORCID,Abhyankar Sunil7,Ponce Doris M.8ORCID,DeFilipp Zachariah9ORCID,Kitko Carrie L.10,Adekola Kehinde11ORCID,Reshef Ran12,Ayuk Francis13,Capellini Alexandra2,Chanswangphuwana Chantiya14,Eder Matthias15,Eng Gilbert2,Gandhi Isha2ORCID,Grupp Stephan16,Gleich Sigrun17,Holler Ernst17,Javorniczky Nora Rebeka18,Kasikis Stelios2,Kowalyk Steven2,Morales George2,Özbek Umut19,Rösler Wolf20,Spyrou Nikolaos2ORCID,Yanik Gregory21,Young Rachel2,Chen Yi-Bin9ORCID,Nakamura Ryotaro1ORCID,Ferrara James L. M.2,Levine John E.2ORCID

Affiliation:

1. 1Hematology/Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA

2. 2The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY

3. 3Division of Hematology, Mayo Clinic, Rochester, MN

4. 4Division of Hematology, James Cancer Center, The Ohio State University, Columbus, OH

5. 5Blood and Marrow Transplantation Program, Abramson Cancer Center, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA

6. 6Winship Cancer Institute, Emory University, Atlanta, GA

7. 7Division of Hematologic Malignancies and Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS

8. 8Division of Hematology/Oncology, Department of Medicine, Adult Bone Marrow Transplantation Service, Memorial Sloan Kettering, New York, NY

9. 9Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA

10. 10Pediatric Stem Cell Transplant Program, Vanderbilt University Medical Center, Nashville, TN

11. 11Division of Hematology/Oncology, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL

12. 12Blood and Marrow Transplantation, Columbia University Medical Center, New York, NY

13. 13Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

14. 14Department of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Bangkok, Thailand

15. 15Department of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany

16. 16Division of Oncology, The Children’s Hospital of Philadelphia, Philadelphia, PA

17. 17Department of Hematology and Oncology, Internal Medicine III, University of Regensburg, Regensburg, Germany

18. 18Department of Medicine I, Medical Center - University of Freiburg, Faculty of Medicine, Albert Ludwigs University, Freiburg, Germany

19. 19Department of Population Health Science and Policy, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY

20. 20Department of Internal Medicine 5, University Hospital Erlangen, Erlangen, Germany

21. 21Blood and Marrow Transplant Program, Michigan Medicine, Ann Arbor, MI

Abstract

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 α4β7 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.

Publisher

American Society of Hematology

Subject

Hematology

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