Impact of Conditioning Intensity and Genomics on Relapse After Allogeneic Transplantation for Patients With Myelodysplastic Syndrome.


Journal

JCO precision oncology
ISSN: 2473-4284
Titre abrégé: JCO Precis Oncol
Pays: United States
ID NLM: 101705370

Informations de publication

Date de publication:
2021
Historique:
received: 31 08 2020
revised: 09 11 2020
accepted: 14 12 2020
entrez: 26 5 2021
pubmed: 27 5 2021
medline: 27 5 2021
Statut: epublish

Résumé

Patients with myelodysplastic syndrome (MDS) are at risk of relapse after allogeneic hematopoietic cell transplantation. The utility of ultra-deep genomic testing to predict and the impact of conditioning intensity to prevent MDS relapse are unknown. Targeted error-corrected DNA sequencing was performed on preconditioning blood samples from patients with MDS (n = 48) from the Blood and Marrow Transplant Clinical Trials Network 0901 phase III randomized clinical trial, which compared outcomes by allogeneic hematopoietic cell transplantation conditioning intensity in adult patients with < 5% marrow myeloblasts and no leukemic myeloblasts in blood on morphological analysis at the time of pretransplant assessment. Clinical end points (53-month median follow-up) included transplant-related mortality (TRM), relapse, relapse-free survival (RFS), and overall survival (OS). Of the 48 patients examined, 14 experienced TRM, 23 are relapse-free, and 11 relapsed, of which 7 died. Using a previously described set of 10 gene regions, 42% of patients (n = 20) had mutations detectable before random assignment to reduced intensity conditioning (RIC) or myeloablative conditioning (MAC). Testing positive was associated with increased rates of relapse (3-year relapse, 40% This study provides evidence that targeted DNA sequencing in patients with MDS before transplant can identify those with highest post-transplant relapse rates. In those testing positive, random assignment to MAC lowered but did not eliminate relapse risk.

Identifiants

pubmed: 34036237
doi: 10.1200/PO.20.00355
pii: PO.20.00355
pmc: PMC8140814
pii:
doi:

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural Research Support, U.S. Gov't, P.H.S.

Langues

eng

Subventions

Organisme : NHLBI NIH HHS
ID : UG1 HL069290
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL069274
Pays : United States
Organisme : NHLBI NIH HHS
ID : U24 HL138660
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL069294
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL069246
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL069274
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL138658
Pays : United States

Informations de copyright

© 2021 by American Society of Clinical Oncology.

Déclaration de conflit d'intérêts

The following represents disclosure information provided by authors of this manuscript. All relationships are considered compensated unless otherwise noted. Relationships are self-held unless noted. I = Immediate Family Member, Inst = My Institution. Relationships may not relate to the subject matter of this manuscript. For more information about ASCO’s conflict of interest policy, please refer to www.asco.org/rwc or ascopubs.org/cci/author-center. Open Payments is a public database containing information reported by companies about payments made to US-licensed physicians (Open Payments). No potential conflicts of interest were reported.

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Auteurs

Laura W Dillon (LW)

Laboratory of Myeloid Malignancies, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD.

Gege Gui (G)

Laboratory of Myeloid Malignancies, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD.

Brent R Logan (BR)

Medical College of Wisconsin, Milwaukee, WI.

Mingwei Fei (M)

Medical College of Wisconsin, Milwaukee, WI.

Jack Ghannam (J)

Laboratory of Myeloid Malignancies, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD.

Yuesheng Li (Y)

Laboratory of Myeloid Malignancies, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD.

Abel Licon (A)

ArcherDX, Boulder, CO.

Edwin P Alyea (EP)

Dana Farber Cancer Institute, Boston, MA.

Asad Bashey (A)

Blood and Marrow Transplant Program at Northside Hospital, Atlanta, GA.

Steven M Devine (SM)

National Marrow Donor Program and Center for International Blood and Marrow Transplant Research, Minneapolis, MN.

Hugo F Fernandez (HF)

Moffitt Cancer Center and Research Institute, Tampa, FL.

Sergio Giralt (S)

Memorial Sloan Kettering Cancer Center, New York, NY.

Mehdi Hamadani (M)

West Virginia University Medicine, Morgantown, WV.

Alan Howard (A)

National Marrow Donor Program and Center for International Blood and Marrow Transplant Research, Minneapolis, MN.

Richard T Maziarz (RT)

Knight Cancer Institute, Oregon Health & Science University, Portland, OR.

David L Porter (DL)

University of Pennsylvania, Philadelphia, PA.

Erica D Warlick (ED)

University of Minnesota, Minneapolis, MN.

Marcelo C Pasquini (MC)

Medical College of Wisconsin, Milwaukee, WI.

Bart L Scott (BL)

Fred Hutchinson Cancer Research Center, Seattle, WA.

Mitchell E Horwitz (ME)

Duke University, Durham, NC.

H Joachim Deeg (HJ)

Fred Hutchinson Cancer Research Center, Seattle, WA.

Christopher S Hourigan (CS)

Laboratory of Myeloid Malignancies, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD.

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Classifications MeSH