Safety and survival outcomes for bloodless transplantation in patients with myeloma.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
15 01 2019
Historique:
received: 29 01 2018
revised: 01 04 2018
accepted: 18 05 2018
pubmed: 28 11 2018
medline: 28 10 2019
entrez: 28 11 2018
Statut: ppublish

Résumé

High-dose therapy (HDT) and autologous stem cell transplantation (ASCT) are established components in the treatment of multiple myeloma; however, undergoing transplantation usually requires hematopoietic support, which poses a challenge among patients who are unwilling to receive blood products. Most transplant centers decline HDT/ASCT to these patients because of safety concerns. Here, the authors' institutional data on safety, engraftment parameters, and survival outcomes after bloodless ASCT (BL-ASCT) are examined among patients with myeloma. This retrospective case-control study included patients who underwent BL-ASCT and Transfusion-supported ASCT (TS-ASCT) at Emory University Hospital between August 2006 and August 2016. In total, 24 patients who underwent BL-ASCT and 70 who underwent TS-ASCT were included. The median time for neutrophil engraftment, platelet engraftment and the median length of hospital stay all were equivalent for both groups. There were no transplant-related cardiovascular complications or mortality in either the BL-ASCT group or the TS-ASCT group. The median progression-free survival was 36 months and 44 months in the BL-ASCT and TS-ASCT groups, respectively (P = .277), and the median OS was not reached in either group at a median follow-up of 59 months after ASCT (P = .627). There was no transplant-related mortality at the 100-day or 1-year mark in either group. BL-ASCT is safe and feasible; transplant-related mortality, cardiovascular and hematologic complications are similar to those associated with TS-ASCT. Furthermore, BL-ASCT can yield similar engraftment and survival parameters comparable to those observed with TS-ASCT.

Identifiants

pubmed: 30480777
doi: 10.1002/cncr.31677
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

185-193

Informations de copyright

© 2018 American Cancer Society.

Auteurs

Nisha S Joseph (NS)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

Jonathan L Kaufman (JL)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

Lawrence H Boise (LH)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

Kelly Valla (K)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

Dhwani K Almaula (DK)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

Chikaodili O Obidike (CO)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

Amelia A Langston (AA)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

Edmund K Waller (EK)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

Hanna J Khoury (HJ)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

Christopher R Flowers (CR)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

Michael Graiser (M)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

Leonard T Heffner (LT)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

Sagar Lonial (S)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

Ajay K Nooka (AK)

Department of Hematology and Oncology Winship Cancer Institute, Emory University, Atlanta, Georgia.

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