| Literature DB >> 34152404 |
Parastoo B Dahi1,2, Jasme Lee3, Sean M Devlin3, Josel Ruiz1, Molly Maloy1, Carlos Rondon-Clavo1, Erica Petrlik1, Roni Tamari1,2, Gunjan Shah1,2, Michael Scordo1,2, Matthew J Matasar2,4, Paul A Hamlin2,4, Esperanza Papadopoulos1,2, Ann A Jakubowski1,2, Miguel-Angel Perales1,2, Craig H Moskowitz5, Craig S Sauter1,2, Sergio A Giralt1,2.
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.Entities:
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Year: 2021 PMID: 34152404 DOI: 10.1182/bloodadvances.2020004167
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529