High-Dose Chemotherapy and Autologous Stem Cell Transplantation for Relapsed or Refractory Primary Mediastinal Large B-Cell Lymphoma.
Adult
Humans
Hematopoietic Stem Cell Transplantation
/ methods
Rituximab
/ therapeutic use
Vorinostat
Retrospective Studies
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Melphalan
/ therapeutic use
Neoplasm Recurrence, Local
/ drug therapy
Transplantation, Autologous
Lymphoma, Large B-Cell, Diffuse
/ diagnostic imaging
Thymus Neoplasms
/ drug therapy
Autologous stem cell transplantation
High-dose chemotherapy
Primary mediastinal large B cell lymphoma
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:
Nov 2023
Nov 2023
Historique:
received:
23
06
2023
revised:
02
08
2023
accepted:
16
08
2023
medline:
3
11
2023
pubmed:
23
8
2023
entrez:
22
8
2023
Statut:
ppublish
Résumé
Primary mediastinal large B-cell lymphoma (PMBCL) is an uncommon, aggressive type of non-Hodgkin lymphoma. Rituximab-containing chemoimmunotherapy with or without radiation therapy (RT) is standard first-line treatment. Relapsed or refractory (R/R) disease has long been treated with salvage chemotherapy followed by high-dose chemotherapy (HDC), with autologous stem cell transplantation (ASCT) in appropriate patients. We retrospectively analyzed all patients with R/R PMBCL treated with HDC/ASCT at our center between January 2000 and August 2022. The 60 study patients received either rituximab-BEAM (n = 37) or rituximab-gemcitabine/busulfan/melphalan (R-GemBuMel) with or without vorinostat (n = 23), followed by ASCT. Forty-six patients received mediastinal RT, either as prior consolidation of frontline therapy or following ASCT. At median follow-up of 6 years (range, .3 to 21 years), the 5-year progression-free survival (PFS) and overall survival (OS) rates of the whole group were 58% and 77%, respectively, for the entire cohort, 51% and 65% for the R-BEAM recipients, and 69% and 82% for R-vorinostat/GemBuMel recipients. Multivariable analyses showed that a negative positron emission tomography scan at ASCT (hazard ratio [HR], .28) and involvement of only 1 organ (HR, .33) were independently associated with improved PFS. In addition, receipt of R-vorinostat/GemBuMel (HR, .23) was an independent favorable predictor of OS. Our data indicate that HDC/ASCT is effective in R/R PMBCL, with improved outcomes in patients receiving R-vorinostat/GemBuMel.
Identifiants
pubmed: 37607645
pii: S2666-6367(23)01500-2
doi: 10.1016/j.jtct.2023.08.019
pii:
doi:
Substances chimiques
Rituximab
4F4X42SYQ6
Vorinostat
58IFB293JI
Melphalan
Q41OR9510P
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
690-694Informations de copyright
Copyright © 2023 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.