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 session3085 - Sequential therapy with bevacizumab and epidermal growth factor receptor-directed agents for metastatic colorectal carcinoma: a retrospective, registry-based analysisPresenter: Tomas Buchler Session: Poster display session Resources: Abstract 3551 - Outcomes in patients receiving maintenance therapy in two panitumumab (Pmab) first-line trials for metastatic colorectal cancer (mCRC)Presenter: Fernando Rivera Herrero Session: Poster display session Resources: Abstract 2191 - AMALTHEA: A prospective, single-arm study of the Hellenic Cooperative Oncology Group evaluating the efficacy and safety of 1st line FOLFIRI+Aflibercept in patients with metastatic colorectal cancer.Presenter: George Pentheroudakis Session: Poster display session Resources: Abstract Slides 2559 - Multicenter phase II study of biweekly XELIRI plus Bevacizumab as a second-line therapy in patients with metastatic colorectal cancer (JSWOG-C3 study)Presenter: Yoshiko Mori Session: Poster display session Resources: Abstract 3760 - Sex-related differences in circadian-dependent tolerance of Irinotecan (I) added to chronomodulated (chrono) 5-Fluorouracil (F), Leucovorin (L) and Oxaliplatin (O): final results from international randomised time-finding study in patients with metastatic colorectal cancer (MCC).Presenter: Francis Levi Session: Poster display session Resources: Abstract 4280 - Mechanism of Pelareorep (Pel)-mediated cell death in a Phase I study in combination with irinotecan/ fluorouracil/ leucovorin/ bevacizumab (FOLFIRI/B) in patients with KRAS mutant metastatic colorectal cancer (mCRC)Presenter: SANJAY GOEL Session: Poster display session Resources: Abstract 2889 - Bevacizumab first line and impact on subsequent anti-EGFR activity.Presenter: Timothy Price Session: Poster display session Resources: Abstract 5158 - Efficacy of anti-EGFR antibodies combined with chemotherapy for elderly patients with RAS wild-type Metastatic Colorectal Cancer: A Systematic Review and Metanalysis.Presenter: Lorenzo Belluomini Session: Poster display session Resources: Abstract 5502 - Efficacy of panitumumab and cetuximab in elderly patients (aged ≥75) with chemotherapy-refractory wild-type KRAS exon 2 metastatic colorectal cancer (mCRC): retrospective analysis of data from nationwide Drug-Reimbursement-Access ProgramPresenter: Marcin Swierkowski Session: Poster display session Resources: Abstract 3493 - Toxicity and efficacy of flat-dosed versus body-surface area (BSA)-dosed capecitabinePresenter: Femke Man 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.
|