Clinical outcomes after idecabtagene vicleucel in older patients with multiple myeloma: a multicenter real-world experience

被引:2
作者
Kalariya, Nilesh M. [1 ]
Hildebrandt, Michelle A. T. [1 ]
Hansen, Doris K. [2 ]
Sidana, Surbhi [3 ]
Khouri, Jack [4 ]
Ferreri, Christopher J. [5 ]
Doyle, William N. [2 ]
Castaneda-Puglianini, Omar [2 ]
Freeman, Ciara L. [2 ]
Hovanky, Vanna [3 ]
Hosoya, Hitomi [3 ]
Shune, Leyla O. [6 ]
Patel, Krina K. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr Houston, Dept Lymphoma & Myeloma, 1515 Holcombe Blvd,Unit 0429, Houston, TX 77030 USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Blood & Marrow Transplant & Cellular Immunotherapy, Tampa, FL USA
[3] Stanford Univ, Sch Med, Stanford, CA USA
[4] Cleveland Clin, Taussig Canc Ctr, Cleveland, OH USA
[5] Wake Forest Univ, Sch Med, Levine Canc Inst, Atrium Hlth, Charlotte, NC USA
[6] Univ Kansas Med Ctr, Kansas City, KS USA
关键词
T-CELL THERAPY; SURVIVAL; TRENDS; BCMA; AGE;
D O I
10.1182/bloodadvances.2024013540
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The safety and efficacy of chimeric antigen receptor T-cell therapy is not well described in older patients, a population that has higher frailty and comorbidities. In this multicenter retrospective study, we evaluated clinical outcomes along with frailty and geriatric characteristics such as comorbidities, polypharmacy, falls, neuropathy, organ dysfunction, and performance status in younger (aged <65 years) vs older (aged >= 65 years) patients who received commercial idecabtagene vicleucel (ide-cel). A total of 156 patients (n = 75, aged >= 65 years) were infused with ide-cel by data cutoff. In older patients (median age: 69 years; range, 65-83; 66.7% frail; 77.3% did not meet KarMMa eligibility criteria), with a median follow-up duration of 14.2 months, best overall response rate (ORR) was 86.7%, which was comparable with pivotal KarMMa study results (ORR: 73%). Median progression-free survival and overall survival in older patients were 9.1 months and 26.5 months, respectively. Grade >= 3 cytokine-release syndrome and immune effector cell-associated neurotoxicity syndrome were observed in 1% and 4% of older patients, respectively. Compared with younger patients, the older patients had significantly higher prevalence of frailty, geriatric characteristics such as polypharmacy (>= 5 drugs; 97%), >= 4 comorbidities (69%), and organ dysfunction (35%; P < .05). The safety and efficacy of ide-cel therapy were similar in younger and older patients. Frailty and geriatric characteristics such as polypharmacy, comorbidities, and organ dysfunction in older patients did not confer an inferior overall outcome.
引用
收藏
页码:4679 / 4688
页数:10
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