Survival Outcomes of Younger Patients With Mantle Cell Lymphoma Treated in the Rituximab Era.
Adult
Age Factors
Aged
Antineoplastic Agents, Immunological
/ adverse effects
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Female
Hematopoietic Stem Cell Transplantation
/ adverse effects
Humans
Lymphoma, Mantle-Cell
/ mortality
Male
Middle Aged
North America
Progression-Free Survival
Retrospective Studies
Risk Assessment
Risk Factors
Rituximab
/ adverse effects
Time Factors
Transplantation, Autologous
Young Adult
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 02 2019
20 02 2019
Historique:
pubmed:
8
1
2019
medline:
18
12
2019
entrez:
8
1
2019
Statut:
ppublish
Résumé
Mantle cell lymphoma (MCL) is a B-cell lymphoma characterized by cyclin D1 expression. Autologous hematopoietic cell transplantation (AHCT) consolidation after induction chemotherapy is often used for eligible patients; however, the benefit remains uncertain in the rituximab era. Herein we retrospectively assessed the impact of AHCT consolidation on survival in a large cohort of transplantation-eligible patients age 65 years or younger. We retrospectively studied transplantation-eligible adults age 65 years or younger with newly diagnosed MCL treated between 2000 and 2015. The primary objective was to assess for improved progression-free survival (PFS) with AHCT consolidation and secondarily to assess for improved overall survival (OS). Cox multivariable regression analysis and propensity score-weighted (PSW) analysis were performed. Data were collected from 25 medical centers for 1,254 patients; 1,029 met inclusion criteria. Median follow-up for the cohort was 76 months. Median PFS and OS were 62 and 139 months, respectively. On unadjusted analysis, AHCT was associated with improved PFS (75 v 44 months with v without AHCT, respectively; P < .01) and OS (147 v 115 months with v without AHCT, respectively; P < .05). On multivariable regression analysis, AHCT was associated with improved PFS (hazard ratio [HR], 0.54; 95% CI, 0.44 to 0.66; P < .01) and a trend toward improved OS (HR, 0.77; 95% CI, 0.59 to 1.01; P = .06). After PSW analysis, AHCT remained associated with improved PFS (HR, 0.70; 95% CI, 0.59 to 0.84; P < .05) but not improved OS (HR, 0.87; 95% CI, 0.69 to 1.1; P = .2). In this large cohort of younger, transplantation-eligible patients with MCL, AHCT consolidation after induction was associated with significantly improved PFS but not OS after PSW analysis. Within the limitations of a retrospective analysis, our findings suggest that in younger, fit patients, AHCT consolidation may improve PFS.
Identifiants
pubmed: 30615550
doi: 10.1200/JCO.18.00690
pmc: PMC7554677
doi:
Substances chimiques
Antineoplastic Agents, Immunological
0
Rituximab
4F4X42SYQ6
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
471-480Subventions
Organisme : NCI NIH HHS
ID : P30 CA006927
Pays : United States
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