Abstract 1443
Background
SCHOLAR-1 (Crump, ASCO 2016) is a large, pooled analysis of rNHL and demonstrated poor outcomes: objective response rate (ORR)= 26%; complete response (CR)=8%. ZUMA-1 is the first, multicenter trial of anti-CD19 CAR T cells (axi-cel) in rNHL and reported positive results: ORR= 82%; CR = 54%. This is a comparative analysis of outcomes from ZUMA-1 and SCHOLAR-1 after adjusting for imbalances in key covariates of patients enrolled.
Methods
Eligible pts for both studies had rNHL (stable disease ≤6 mos with ≥4 cycles frontline or ≥ 2 cycles later-line therapy, progressive disease as best response, or relapse ≤12 mos post autologous stem cell transplant). Standardized analyses were performed to account for other baseline covariates that were imbalanced between the studies despite similar inclusion criteria. These analyses equally weighted the proportions of patients with select prognostic covariates between the two studies. The pre-specified covariates selected for weighting were refractory subgroup and occurrence of SCT after refractory status. Sensitivity analyses included additional covariates.
Results
101 ZUMA-1 pts received axi-cel; SCHOLAR-1 included data from 508 pts. Baseline characteristics for each study are listed in the Table. ZUMA-1 median follow-up was 8.7 mos. Using the standardized analysis, the estimated ORR and CR rates in SCHOLAR-1 were 20% and 6%, respectively. Standardized 6-mo survival rate for SCHOLAR-1 was 35%. Risk of death in ZUMA-1 was reduced by 77% relative to SCHOLAR-1 (P < .0001).Table:
1161P
ZUMA-1 mITT | SCHOLAR-1 Response | |
---|---|---|
N = 101 | N = 508 | |
Age, ≥65 y, n (%) | 24 (24) | 74 (15) |
Refractory subgroup, n (%) | ||
Primary refractory | 2 (2) | 101 (20) |
Refractory to ≥ 2L | 78 (77) | 316 (62) |
Relapse ConclusionsDespite the imbalances between the ZUMA-1 and SCHOLAR-1 studies, axi-cel appears to represent a significantly improved treatment option for pts with rNHL compared with currently available therapies as used in the SCHOLAR-1 study. Clinical trial identificationNCT02348216 Legal entity responsible for the studyKite Pharma FundingKite Pharma DisclosureS.S. Neelapu: Kite research funding, consultant and advisory board member for Kite. F.L. Locke: Scientific advisory board and Moffitt receives research funding from Kite Pharma; Consultant for Cellular Biomedicine Group, Inc. P.M. Reagan: Research Funding: Seattle Genetics. D. Miklos, C.A. Jacobson: Consulting or Advisory Role: PCYC, Sanofi, Adaptive Biotechnologies, Kite, Genentech, Velos; Research Funding: PCYC; Patents: PCYC; Travel Accommodations: PCYC, Sanofi I. Braunschweig: Stock/Equity Ownership: Kite Pharma. T. Siddiqi: Speaker\'s bureau for Pharmacyclics/Jannsen (ibrutinib) and Seattle Genetics (brentuximab vedotin). Y. Lin: Employment: Mayo Clinic; Research funding: Janssen. J. Kuruvilla: Research funding: Celgene, Roche, Karyopharm; consultant: Bristol-Myers Squib, Gilead, Janssen, Hoffman LaRoche, Seattle Genetics; honoraria: Amgen, Bristol-Myers Squibb, Celgene, Gilead, Roche, Janssen, Lundbeck, Merck, Seattle Genetics, B.K. Link, U. Farooq: Research Funding: Kite Pharma. L. Navale, W.Y. Go: Employment: Kite Pharma. J. Wiezorek: Leadership: Kite Pharma. All other authors have declared no conflicts of interest. Resources from the same session3660 - Tumor-stroma interactions and response to targeted agents in preclinical models of colorectal cancer (CRC)Presenter: Chiara Bazzichetto Session: Poster display session Resources: Abstract 2831 - Molecular profiling of colorectal tumors stratified by the histological tumor-stroma ratioPresenter: Tessa Sandberg Session: Poster display session Resources: Abstract 4988 - The Characteristics and Prognostic Factors in Colorectal Cancer Containing Signet Ring CellPresenter: Xiang Quan Kong Session: Poster display session Resources: Abstract 1844 - Effect of lateral lymph node dissection for lower rectal cancer: An ad hoc analysis of the ACTS-RC randomized clinical trialPresenter: Eiji Oki Session: Poster display session Resources: Abstract 4371 - Effects of mesorectal fascia (MRF) status for locally advanced rectal cancer: Results of a multicenter, randomized, controlled, phase II trial (FDRT-002)Presenter: Ji Zhu Session: Poster display session Resources: Abstract 2018 - Planned organ preservation for selected T2, T3 rectal cancer. French experience using chemo radiotherapy and Contact X Ray boostPresenter: Jean-Pierre Gérard Session: Poster display session Resources: Abstract 2891 - Comparison between magnetic resonance imaging (MRI) and pathology in the assessment of tumour regression grade (TRG) in rectal cancer (RC)Presenter: Francesco Sclafani Session: Poster display session Resources: Abstract 4031 - FOLFIRINOX as induction treatment in rectal cancer patients with synchronous metastases (RCSM): final results of the FFCD 1102 phase II trial.Presenter: Jean-Baptiste BACHET Session: Poster display session Resources: Abstract 3864 - Neoadjuvant treatment with mFOLFOXIRI alone versus chemoradiotherapy in locally advanced rectal cancer: A Propensity Score Analysis from two prospective trialsPresenter: JianWei Zhang Session: Poster display session Resources: Abstract 1429 - Updated survival results of FACT trial: Multicenter phase II trial of neoadjuvant chemotherapy with mFOLFOX6 for stage II/III rectal cancer with a T3/T4 tumor.Presenter: Hirotoshi Hasegawa Session: Poster display session Resources: Abstract This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used. For more detailed information on the cookies we use, please check our Privacy Policy.
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