A Prospective Cohort Study Comparing Long-Term Outcomes with and without Palifermin in Patients Receiving Hematopoietic Cell Transplantation for Hematologic Malignancies.


Journal

Transplantation and cellular therapy
ISSN: 2666-6367
Titre abrégé: Transplant Cell Ther
Pays: United States
ID NLM: 101774629

Informations de publication

Date de publication:
10 2021
Historique:
received: 30 04 2021
revised: 22 06 2021
accepted: 27 06 2021
pubmed: 6 7 2021
medline: 21 10 2021
entrez: 5 7 2021
Statut: ppublish

Résumé

The incidence of debilitating oral mucositis (OM) can be as high as 99% after myeloablative conditioning regimens preparing patients with hematologic malignancies for hematopoietic cell transplantation (HCT). Palifermin (KGF) is a recombinant human keratinocyte growth factor that reduces the incidence and duration of severe OM. The long-term safety of KGF has not been well established, however. In this long-term prospective matched-cohort study, patients who received KGF (cases) and underwent autologous or allogeneic HCT for hematologic malignancies between 2006 and 2013 were matched 1:1 to patients who did not receive KGF (controls). The primary outcome was overall survival (OS). Other outcomes were disease relapse, new malignancies, pancreatitis, renal failure requiring dialysis, pulmonary complications, cataract surgery, and acute and chronic graft-versus-host disease (GVHD). The analysis population comprised 2191 matched pairs with a wide range of diseases and donor types that received diverse conditioning and GVHD preventive regimens, representing contemporary practice patterns. The median duration of follow-up was 8 years (range, 1 to 12.5 years). In multivariate analyses, the probabilities of OS (relative risk [RR], 1.01; 95% confidence interval [CI], 0.91 to 1.12), relapse (RR, 1.06; 95% CI, 0.94 to 1.18), new malignancies (RR, 0.89; 95% CI, 0.67 to 1.18), and cataract surgery (RR, 1.05; 95% CI, 0.74 to 1.50) were not statistically significantly different between cases and controls. In univariate analyses, no increased risks were observed for renal failure requiring dialysis, pancreatitis, acute GVHD, chronic GVHD, interstitial pneumonitis/acute respiratory distress syndrome/idiopathic pneumonia syndrome, or bronchiolitis obliterans/cryptogenic organizing pneumonia/bronchiolitis obliterans organizing pneumonia among cases compared with controls. This long-term prospective safety cohort study demonstrates that the KGF group had no increased risk of overall mortality, relapse, new malignancies, or any other key outcome. The broad inclusion criteria allow the results to be generalized to contemporary practice for patients with a wide range of diseases and receiving a wide range of HCT conditioning regimens and graft sources from diverse donor types.

Identifiants

pubmed: 34224914
pii: S2666-6367(21)01031-9
doi: 10.1016/j.jtct.2021.06.028
pmc: PMC8606163
mid: NIHMS1733777
pii:
doi:

Substances chimiques

Fibroblast Growth Factor 7 126469-10-1

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

837.e1-837.e10

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : U24 CA076518
Pays : United States

Informations de copyright

Copyright © 2021 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement M.R. is an employee and shareholder of Sobi. J.R.W. receives consulting fees from Celgene, Shire, Janssen, Ansun, Merck, Cidara, and Reveal. M.A.P. reports honoraria from AbbVie, Astellas, Bellicum, Celgene, Bristol-Myers Squibb, Incyte, Kite/Gilead, Merck, Miltenyi Biotec, Novartis, Nektar Therapeutics, Omeros, and Takeda. He serves on data monitoring and safety boards for Cidara Therapeutics, Servier, and Medigene and on the scientific advisory boards of MolMed and NexImmune. He has received research support for clinical trials from Incyte, Kite/Gilead, Miltenyi Biotec, and Novartis. S.F. reports grant/research support, consultant, stock/shareholder for Mustang Bio; he is a board member for Lixte Bio. The other authors have no conflicts of interest to disclose.

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Auteurs

Wael Saber (W)

Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin. Electronic address: wsaber@mcw.edu.

Patricia Steinert (P)

Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.

Mei-Jie Zhang (MJ)

Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin; Division of Biostatistics, Institute for Health and Equity, Medical College of Wisconsin, Milwaukee, Wisconsin.

Min Chen (M)

Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.

Andrea Pope (A)

Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.

Armand Keating (A)

Princess Margaret Cancer Center-BMT Program, Toronto, Ontario, Canada.

John R Wingard (JR)

Division of Hematology & Oncology, Department of Medicine, University of Florida, Gainesville, Florida.

Karen Ballen (K)

Division of Hematology/Oncology, University of Virginia Health System, Charlottesville, Virginia.

Patrick Stiff (P)

Division of Hematology/Oncology, Loyola University Medical Center, Maywood, Illinois.

Miguel-Angel Perales (MA)

Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Stephen Forman (S)

Department of Hematology & Hematopoietic Cell Transplantation, City of Hope, Duarte, California.

Richard Champlin (R)

Department of Stem Cell Transplantation and Cellular Therapy, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Amelia Langston (A)

Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, Georgia.

Mattias Rudebeck (M)

Swedish Orphan Biovitrum, Stockholm, Sweden.

Mary Horowitz (M)

Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.

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