Comparative effectiveness of ZUMA-5 (axi-cel) vs SCHOLAR-5 external control in relapsed/refractory follicular lymphoma

被引:45
作者
Ghione, Paola [1 ,2 ]
Palomba, M. Lia [2 ]
Patel, Anik R. [3 ]
Bobillo, Sabela [4 ]
Deighton, Kevin [5 ]
Jacobson, Caron A. [6 ]
Nahas, Myrna [3 ]
Hatswell, Anthony J. [5 ]
Jung, A. Scott [3 ]
Kanters, Steve [7 ]
Snider, Julia Thornton [3 ]
Neelapu, Sattva S. [8 ]
Ribeiro, Maria Teresa [9 ]
Brookhart, M. Alan [10 ,11 ]
Ghesquieres, Herve [12 ]
Radford, John [13 ,14 ]
Gribben, John G. [15 ]
机构
[1] Roswell Pk Comprehens Canc Ctr, Buffalo, NY USA
[2] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[3] Kite, Santa Monica, CA USA
[4] Univ Hosp Vall dHebron, Vall DHebron Inst Oncol, Dept Haematol, Barcelona, Spain
[5] Delta Hat, Nottingham, England
[6] Dana Farber Canc Inst, Boston, MA 02115 USA
[7] RainCity Analyt, Vancouver, BC, Canada
[8] Univ Texas MD Anderson Canc Ctr, Div Canc Med, Dept Lymphoma & Myeloma, Houston, TX 77030 USA
[9] Portuguese Oncol Inst Porto, Porto, Portugal
[10] Target Real World Evidence RWE, Durham, NC USA
[11] Duke Univ, Dept Populat Hlth Sci, Durham, NC USA
[12] Hop Lyon Sud, Lyon, France
[13] Christie Natl Hlth Serv NHS Fdn Trust, Manchester, Lancs, England
[14] Univ Manchester, Div Canc Sci, Manchester, Lancs, England
[15] Queen Mary Univ London, Ctr Haematooncol, Barts Canc Inst, London, England
关键词
OUTCOMES; TRIAL; RISK;
D O I
10.1182/blood.2021014375
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the pivotal ZUMA-5 trial, axicabtagene ciloleucel (axi-cel; an autologous anti-CD19 chimeric antigen receptor T-cell therapy) demonstrated high rates of durable response in relapsed/refractory (r/r) follicular lymphoma (FL) patients. Here, outcomes from ZUMA-5 are compared with the international SCHOLAR-5 cohort, which applied key ZUMA-5 trial eligibility criteria simulating randomized controlled trial conditions. SCHOLAR-5 data were extracted from institutions in 5 countries, and from 1 historical clinical trial, for r/r FL patients who initiated a third or higher line of therapy after July 2014. Patient characteristics were balanced through propensity scoring on prespecified prognostic factors using standardized mortality ratio (SMR) weighting. Time-to-event outcomes were evaluated using weighted Kaplan-Meier analysis. Overall response rate (ORR) and complete response (CR) rate were compared using weighted odds ratios. The 143 ScHOLAR-5 patients reduced to an effective sample of 85 patients after SMR weighting vs 86 patients in ZUMA-5. Median follow-up time was 25.4 and 23.3 months for SCHOLAR-5 and ZUMA-5. Median overall survival (OS) and progression-free survival (PFS) in SCHOLAR-5 were 59.8 months reached in ZUMA-5. Hazard ratios for OS and PFS were 0.42 (95% confidence interval [CI], 0.21-0.83) and 0.30 (95% CI, 0.18-0.49). The ORR and CR rate were 49.9% and 29.9% in SCHOLAR-5 and 94.2% and 79.1% in ZUMA-5, for odds ratios of 16.2 (95% CI, 5.6-46.9) and 8.9 (95% CI, 4.3-18.3). Compared with available therapies, axi-cel demonstrated an improvement in meaningful clinical endpoints, suggesting axi-cel addresses an important unmet need for r/r FL patients.
引用
收藏
页码:851 / 860
页数:10
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