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Toxicities of high-dose chemotherapy and autologous hematopoietic cell transplantation in older patients with lymphoma.

Authors :
Dahi PB
Lee J
Devlin SM
Ruiz J
Maloy M
Rondon-Clavo C
Petrlik E
Tamari R
Shah G
Scordo M
Matasar MJ
Hamlin PA
Papadopoulos E
Jakubowski AA
Perales MA
Moskowitz CH
Sauter CS
Giralt SA
Source :
Blood advances [Blood Adv] 2021 Jun 22; Vol. 5 (12), pp. 2608-2618.
Publication Year :
2021

Abstract

High-dose chemotherapy and autologous hematopoietic cell transplantation is an effective consolidation therapy in lymphoma; however, its use in elderly patients has been limited because of concerns for greater toxicity in this group. We investigated the toxicities of carmustine, etoposide, cytarabine, and melphalan (BEAM) and autologous hematopoietic cell transplantation (AHCT) in 346 patients in 2 age groups: 279 patients aged 60 to 69 years and 67 patients aged ≥70 years. The majority developed severe toxicities; the most common were febrile neutropenia, gastrointestinal, infections, and cardiovascular. Older patients were at higher risk for grade ≥3 cardiovascular toxicities (hazard ratio [HR], 3.36; 95% confidence interval [CI], 2.25-5.00; P < .001) and skin toxicities (HR, 2.45; 95% CI, 1.08-5.54, P = .032). In the older group, nonrelapse mortality at 100 days and at 2 years was 2.99% (95% CI, 0.55-9.32) and 6.2% (95% CI, 1.97-13.95), respectively, vs 1.79% (95% CI, 0.68-3.92) and 2.91% (95% CI, 1.37-5.42), respectively, in the younger group. When adjusting for the number of grade ≥3 toxicities within the first 100 days, older patients had a 1.71-fold (95% CI, 1.08-2.71) increased risk for progression or death relative to younger patients. Although BEAM followed by AHCT is effective, it is associated with significant organ toxicities, especially in patients aged ≥70 years. Interventions to mitigate toxicities while maintaining efficacy are much needed.<br /> (© 2021 by The American Society of Hematology.)

Details

Language :
English
ISSN :
2473-9537
Volume :
5
Issue :
12
Database :
MEDLINE
Journal :
Blood advances
Publication Type :
Academic Journal
Accession number :
34152404
Full Text :
https://doi.org/10.1182/bloodadvances.2020004167