A Prospective Cohort Study Comparing Long-Term Outcomes with and without Palifermin in Patients Receiving Hematopoietic Cell Transplantation for Hematologic Malignancies.
KGF
Long-term
Malignancies
Mucositis
Palifermin
Safety
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
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.e10Subventions
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.
Références
Biol Blood Marrow Transplant. 2008 Sep;14(9):1017-1021
pubmed: 18721764
Mol Cancer Res. 2008 Aug;6(8):1337-46
pubmed: 18708365
CA Cancer J Clin. 2012 Nov-Dec;62(6):400-22
pubmed: 22972543
J Pediatr Hematol Oncol. 2017 May;39(4):e177-e182
pubmed: 28234746
Blood. 2006 Nov 1;108(9):3216-22
pubmed: 16835378
Biol Blood Marrow Transplant. 2016 Aug;22(8):1460-1466
pubmed: 27090960
Support Care Cancer. 2015 Nov;23(11):3141-7
pubmed: 25791390
Leuk Lymphoma. 2016;57(4):820-7
pubmed: 26428409
Int J Oral Sci. 2014 Mar;6(1):27-30
pubmed: 24357856
N Engl J Med. 2004 Dec 16;351(25):2590-8
pubmed: 15602019
Minerva Stomatol. 2016 Feb;65(1):43-50
pubmed: 26862696
Biol Blood Marrow Transplant. 2016 Jan;22(1):164-9
pubmed: 26303102
Curr Opin Support Palliat Care. 2017 Dec;11(4):341-346
pubmed: 28984677
Lancet. 2002 Apr 13;359(9314):1309-10
pubmed: 11965278
J Dent (Shiraz). 2016 Dec;17(4):343-347
pubmed: 27942550
Curr Opin Oncol. 2015 May;27(3):159-64
pubmed: 25774860
Bone Marrow Transplant. 2014 Sep;49(9):1193-7
pubmed: 25000456
Cancer. 2004 May 1;100(9 Suppl):1995-2025
pubmed: 15108222
Vox Sang. 2019 Oct;114(7):769-777
pubmed: 31402469
Semin Oncol. 2003 Dec;30(6 Suppl 18):76-83
pubmed: 14727245
J Adv Pract Oncol. 2013 Mar;4(2):89-100
pubmed: 25031987
Cochrane Database Syst Rev. 2017 Nov 28;11:CD011990
pubmed: 29181845
Anticancer Res. 2014 Dec;34(12):7379-82
pubmed: 25503176
Cancer. 2014 May 15;120(10):1453-61
pubmed: 24615748
Biol Blood Marrow Transplant. 2016 Jul;22(7):1247-1256
pubmed: 26968792
J Natl Cancer Inst Monogr. 2019 Aug 1;2019(53):
pubmed: 31425598
Support Care Cancer. 2019 Oct;27(10):4011-4022
pubmed: 31286233
J Natl Cancer Inst. 2006 Jun 21;98(12):812-24
pubmed: 16788155
BMJ Support Palliat Care. 2017 Mar;7(1):7-16
pubmed: 25818385
J Oncol Pharm Pract. 2005 Sep;11(3):121-5
pubmed: 16390600