Conditional Long-Term Survival after Autologous Hematopoietic Cell Transplantation for Diffuse Large B Cell Lymphoma.


Journal

Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
ISSN: 1523-6536
Titre abrégé: Biol Blood Marrow Transplant
Pays: United States
ID NLM: 9600628

Informations de publication

Date de publication:
12 2019
Historique:
received: 25 06 2019
revised: 19 08 2019
accepted: 09 09 2019
pubmed: 17 9 2019
medline: 9 9 2020
entrez: 17 9 2019
Statut: ppublish

Résumé

Autologous hematopoietic cell transplantation (AHCT) is standard therapy for patients with chemosensitive, relapsed, diffuse large B cell lymphoma (DLBCL). We performed a retrospective cohort study to delineate subsequent (conditional) and relative survival in 371 adult patients with DLBCL who underwent AHCT between 2000 and 2014 and had survived for 1, 2, 3, or 5 years after transplant. The probability of overall survival at 10 years after AHCT was 62%, 71%, 77%, and 86%, respectively, for the 4 cohorts, whereas that of progression-free survival (PFS) was 55%, 65%, 72%, and 81%, respectively. The respective cumulative incidence of nonrelapse mortality (NRM) at 10 years after transplantation was 13%, 12%, 11%, and 8%, respectively. In multivariable analysis, older age was associated with greater mortality risk among all but 5-year survivors; relapse within the landmark time was associated with greater mortality risk in all groups. Older age and relapse within the landmark time were associated with worse PFS in all groups. Standardized mortality ratio (SMR) was significantly higher than an age-, gender-, and race-matched general population, with the magnitude of SMR decreasing as the landmark time increased (4.0 for 1-year, 3.0 for 2-year, 2.4 for 3-year, and 1.8 for 5-year survivors). Our study provides information on long-term survival and prognosis that will assist in counseling patients with DLBCL who have received AHCT. Survival improves with longer time in remission post-transplant, although patients continue to remain at risk for NRM, underscoring the need for continued vigilance and prevention of late complications.

Identifiants

pubmed: 31525493
pii: S1083-8791(19)30622-6
doi: 10.1016/j.bbmt.2019.09.012
pmc: PMC6900450
mid: NIHMS1542267
pii:
doi:

Types de publication

Clinical Trial Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

2522-2526

Subventions

Organisme : NCI NIH HHS
ID : R01 CA215134
Pays : United States

Informations de copyright

Copyright © 2019 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

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Auteurs

Jessica El-Asmar (J)

Department of Internal Medicine, Cleveland Clinic, Cleveland, Ohio.

Lisa Rybicki (L)

Department of Quantitative Health Sciences, Cleveland Clinic, Cleveland, Ohio.

Brian J Bolwell (BJ)

Blood and Marrow Transplant Program, Cleveland Clinic, Cleveland, Ohio.

Mohamed A Kharfan-Dabaja (MA)

Blood and Marrow Transplant Program, Mayo Clinic, Jacksonville, Florida.

Robert Dean (R)

Blood and Marrow Transplant Program, Cleveland Clinic, Cleveland, Ohio.

Betty K Hamilton (BK)

Blood and Marrow Transplant Program, Cleveland Clinic, Cleveland, Ohio.

Rabi Hanna (R)

Department of Pediatric Hematology, Oncology and Transplantation, Cleveland Clinic, Cleveland, Ohio.

Deepa Jagadeesh (D)

Blood and Marrow Transplant Program, Cleveland Clinic, Cleveland, Ohio.

Matt Kalaycio (M)

Blood and Marrow Transplant Program, Cleveland Clinic, Cleveland, Ohio.

Brad Pohlman (B)

Blood and Marrow Transplant Program, Cleveland Clinic, Cleveland, Ohio.

Ronald Sobecks (R)

Blood and Marrow Transplant Program, Cleveland Clinic, Cleveland, Ohio.

Brian T Hill (BT)

Blood and Marrow Transplant Program, Cleveland Clinic, Cleveland, Ohio.

Navneet S Majhail (NS)

Blood and Marrow Transplant Program, Cleveland Clinic, Cleveland, Ohio. Electronic address: majhain@ccf.org.

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