Biologic Assignment Trial of Reduced-Intensity Hematopoietic Cell Transplantation Based on Donor Availability in Patients 50-75 Years of Age With Advanced Myelodysplastic Syndrome.
Aged
Female
Follow-Up Studies
Graft vs Host Disease
/ etiology
Hematopoietic Stem Cell Transplantation
/ adverse effects
Histocompatibility Testing
Humans
Intention to Treat Analysis
Leukemia
/ therapy
Male
Middle Aged
Myelodysplastic Syndromes
/ therapy
Quality of Life
Survival Rate
Tissue Donors
Transplantation Conditioning
/ methods
Transplantation, Homologous
/ adverse effects
Treatment Outcome
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333
Informations de publication
Date de publication:
20 10 2021
20 10 2021
Historique:
pubmed:
10
6
2021
medline:
15
12
2021
entrez:
9
6
2021
Statut:
ppublish
Résumé
Allogeneic hematopoietic cell transplantation (HCT) is the only potentially curative therapy for myelodysplastic syndromes (MDS), although it is infrequently offered to older patients. The relative benefits of HCT over non-HCT therapy in older patients with higher-risk MDS have not been defined. We conducted a multicenter biologic assignment trial comparing reduced-intensity HCT to hypomethylating therapy or best supportive care in subjects 50-75 years of age with intermediate-2 or high-risk de novo MDS. The primary outcome was overall survival probability at 3 years. Between January 2014 and November 2018, we enrolled 384 subjects at 34 centers. Subjects were assigned to the Donor or No-Donor arms according to the availability of a matched donor within 90 days of study registration. The median follow-up time for surviving subjects was 34.2 months (range: 2.3-38 months) in the Donor arm and 26.9 months (range: 2.4-37.2 months) in the No-Donor arm. In an intention-to-treat analysis, the adjusted overall survival rate at 3 years in the Donor arm was 47.9% (95% CI, 41.3 to 54.1) compared with 26.6% (95% CI, 18.4 to 35.6) in the No-Donor arm ( We observed a significant survival advantage in older subjects with higher-risk MDS who have a matched donor identified and underwent reduced-intensity HCT, when compared with those without a donor. HCT should be included as an integral part of MDS management plans in fit older adults with higher-risk MDS.
Identifiants
pubmed: 34106753
doi: 10.1200/JCO.20.03380
pmc: PMC8791814
doi:
Banques de données
ClinicalTrials.gov
['NCT02016781']
Types de publication
Clinical Trial
Journal Article
Multicenter Study
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
3328-3339Subventions
Organisme : NHLBI NIH HHS
ID : UG1 HL109322
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL108945
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL108987
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL069278
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL069246
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Commentaires et corrections
Type : CommentIn
Références
Lancet Oncol. 2009 Mar;10(3):223-32
pubmed: 19230772
J Natl Cancer Inst. 2008 Nov 5;100(21):1542-51
pubmed: 18957672
Stat Med. 2007 Oct 30;26(24):4505-19
pubmed: 17348080
Blood. 2001 Jan 1;97(1):56-62
pubmed: 11133742
JAMA Oncol. 2020 Apr 1;6(4):486-493
pubmed: 31830234
J Clin Oncol. 2017 Aug 20;35(24):2745-2753
pubmed: 28486043
Lancet. 2002 Apr 13;359(9314):1309-10
pubmed: 11965278
Biol Blood Marrow Transplant. 2014 Oct;20(10):1566-72
pubmed: 24972249
Blood. 1997 Mar 15;89(6):2079-88
pubmed: 9058730
Bone Marrow Transplant. 1997 Feb;19(4):357-68
pubmed: 9051246
J Clin Oncol. 2002 May 15;20(10):2429-40
pubmed: 12011120
Biol Blood Marrow Transplant. 2012 Sep;18(9):1415-21
pubmed: 22579634
Blood Adv. 2019 Nov 26;3(22):3488-3498
pubmed: 31725894
Leukemia. 2015 Jul;29(7):1496-501
pubmed: 25676424
J Clin Oncol. 2010 Feb 1;28(4):586-95
pubmed: 20038732
J Clin Oncol. 2014 Sep 1;32(25):2691-8
pubmed: 25092778
N Engl J Med. 2017 Feb 9;376(6):536-547
pubmed: 28177873
Biol Blood Marrow Transplant. 2012 Jan;18(1):18-36.e6
pubmed: 21803017
Biol Blood Marrow Transplant. 2017 Jun;23(6):971-979
pubmed: 28288952
J Clin Oncol. 2013 Jul 20;31(21):2662-70
pubmed: 23797000
Med Care. 1993 Mar;31(3):247-63
pubmed: 8450681
Blood. 2017 Mar 30;129(13):1753-1762
pubmed: 28096091
Cancer. 2006 Apr 15;106(8):1794-803
pubmed: 16532500
Clin Trials. 2008;5(6):607-16
pubmed: 19029209
Blood. 2012 Jun 21;119(25):6172-3
pubmed: 22730526
Biol Blood Marrow Transplant. 2019 Jan;25(1):114-120
pubmed: 30172776
Blood. 2011 Jan 13;117(2):403-11
pubmed: 20940414
Biol Blood Marrow Transplant. 2018 Jun;24(6):1232-1236
pubmed: 28918304
N Engl J Med. 1998 Dec 3;339(23):1649-56
pubmed: 9834301
J Clin Oncol. 2011 Feb 10;29(5):566-72
pubmed: 21220586
J Clin Oncol. 2010 Apr 10;28(11):1878-87
pubmed: 20212255
Med Care. 2005 Mar;43(3):203-20
pubmed: 15725977
Biol Blood Marrow Transplant. 2009 Dec;15(12):1628-33
pubmed: 19896087
Haematologica. 2017 Dec;102(12):2030-2038
pubmed: 28971906
Int J Epidemiol. 2004 Feb;33(1):15-7
pubmed: 15075139
J Clin Oncol. 2016 Oct 20;34(30):3627-3637
pubmed: 27601546
Blood. 2004 Jul 15;104(2):579-85
pubmed: 15039286
Blood. 2013 Sep 12;122(11):1974-82
pubmed: 23847196
J Clin Oncol. 2011 May 20;29(15):1987-96
pubmed: 21483003
Leukemia. 2003 May;17(5):859-68
pubmed: 12750698
J Clin Oncol. 2011 Aug 20;29(24):3322-7
pubmed: 21788559
Blood Adv. 2018 Aug 28;2(16):2095-2103
pubmed: 30135184
Comput Methods Programs Biomed. 2007 Nov;88(2):95-101
pubmed: 17850917