Adjusted comparison of outcomes between patients from CARTITUDE-1 versus multiple myeloma patients with prior exposure to proteasome inhibitors, immunomodulatory drugs and anti-CD38 antibody from the prospective, multinational LocoMMotion study of real-world clinical practice

被引:12
|
作者
Mateos, Maria-Victoria [1 ]
Weisel, Katja [2 ]
Martin, Thomas [3 ]
Berdeja, Jesus G. [4 ]
Jakubowiak, Andrzej [5 ]
Stewart, A. Keith [6 ,7 ]
Jagannath, Sundar [8 ]
Lin, Yi [9 ]
Diels, Joris [10 ]
Ghilotti, Francesca [11 ]
Thilakarathne, Pushpike [10 ]
Perualila, Nolen J. [10 ]
Cabrieto, Jedelyn [10 ]
Haefliger, Benjamin [12 ]
Erler-Yates, Nichola [13 ]
Hague, Clare [14 ]
Jackson, Carolyn C. [15 ]
Schecter, Jordan M. [15 ]
Strulev, Vadim [16 ]
Nesheiwat, Tonia [17 ]
Pacaud, Lida [17 ]
Einsele, Hermann [18 ]
Moreau, Philippe [19 ]
机构
[1] Univ Hosp Salamanca, IBSAL, CIC, Salamanca, Spain
[2] Univ Med Ctr Hamburg Eppendorf, Hamburg, Germany
[3] UCSF Helen Diller Family Comprehens Canc Ctr, San Francisco, CA USA
[4] Sarah Cannon Res Inst, Nashville, TN USA
[5] Univ Chicago, Chicago, IL USA
[6] Univ Hlth Network, Toronto, ON, Canada
[7] Princess Margaret Canc Ctr, Toronto, ON, Canada
[8] Mt Sinai Med Ctr, New York, NY USA
[9] Mayo Clin, Rochester, MN USA
[10] Janssen Pharmaceut NV, Beerse, Belgium
[11] Janssen Cilag SpA, Cologno Monzese, Italy
[12] Cilag GmbH Int, Zug, Switzerland
[13] Janssen Cilag GmbH, Neuss, Germany
[14] Janssen Cilag NV, High Wycombe, England
[15] Janssen R&D, Raritan, NJ USA
[16] Janssen Pharmaceut NV, EMEA Med Affairs, Beerse, Belgium
[17] Legend Biotech USA Inc, Piscataway, NJ USA
[18] Univ Klinikum Wurzburg, Med Klin & Poliklin II, Wurzburg, Germany
[19] Univ Hosp Hotel Dieu, Clin Hematol, Nantes, France
关键词
PLUS BORTEZOMIB; OPEN-LABEL; PHASE-III; DEXAMETHASONE; POMALIDOMIDE; DIAGNOSIS; PATTERNS; THERAPY;
D O I
10.3324/haematol.2022.280482
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ciltacabtagene autoleucel (cilta-cel) is a chimeric antigen receptor T-cell therapy studied in patients with multiple myeloma exposed to three classes of treatment in the single-arm CARTITUDE-1 study. To assess the effectiveness of cilta-cel compared to real-world clinical practice (RWCP), we performed adjusted comparisons using individual patients' data from CARTITUDE-1 and LocoMMotion, a prospective, multinational study of patients with multiple myeloma triple-class exposed of treatment. Comparisons were performed using inverse probability weighting. In CARTITUDE-1, 113 patients were enrolled, and 97 patients were infused with cilta-cel. In LocoMMotion, 248 patients were enrolled, and 170 patients were included in the comparisons versus infused patients. Ninety-two unique regimens were used in LocoMMotion, most frequently carfilzomib-dexamethasone (13.7%), pomalidomide-cyclophosphamide-dexamethasone (13.3%) and pomalidomidedexamethasone (11.3%). Adjusted comparisons showed that patients treated with cilta-cel were 3.12-fold more likely to respond to treatment than those managed by RWCP (response rate, 3.12, 95% confidence interval [95% CI]: 2.24-4.00), had their risk of progression or death reduced to by 85% (progression-free survival hazard ratio=0.15, 95% CI: 0.08-0.29), and a risk of death lowered by 80% (overall survival hazard ratio HR=0.20, 95% CI: 0.09-0.41). The incremental improvement in health related quality of life from baseline for cilta-cel versus RWCP at week 52, as measured by EORTC QLQ-C30 Global Health Status, was 13.4 (95% CI: 3.5-23.6) and increased to 30.8 (95% CI: 21.8-39.8) when including death as additional information regarding patients' health status. Patients treated with cilta-cel experienced more adverse events than those managed with RWCP (any grade: 100% vs. 83.5%). The results from this study demonstrate improved efficacy outcomes of cilta-cel versus RWCP and highlight its potential as a novel and effective treatment option for patients with multiple myeloma triple-class exposed of antimyeloma treatment. CARTITUDE-1 is registered with clinicaltrials gov. Identifier: NCT03548207. LocoMMotion is registered with clinicaltrials gov. Identifier: NCT04035226.
引用
收藏
页码:2192 / 2204
页数:13
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