Literature DB >> 33449816

Phase II Trial of Costimulation Blockade With Abatacept for Prevention of Acute GVHD.

Benjamin Watkins1, Muna Qayed1, Courtney McCracken2, Brandi Bratrude3, Kayla Betz3, Yvonne Suessmuth1, Alison Yu3, Shauna Sinclair4, Scott Furlan5, Steven Bosinger6, Victor Tkachev3, James Rhodes7, Audrey Grizzle Tumlin7, Alexandria Narayan5, Kayla Cribbin4, Scott Gillespie2, Ted A Gooley5, Marcelo C Pasquini8, Kyle Hebert8, Urvi Kapoor9, Andre Rogatko10, Mourad Tighiouart10, Sungjin Kim10, Catherine Bresee10, Sung W Choi11, Jeffrey Davis12, Christine Duncan3, Roger Giller13, Michael Grimley14, Andrew C Harris15, David Jacobsohn16, Nahal Lalefar17, Maxim Norkin18, Nosha Farhadfar19, Michael A Pulsipher20, Shalini Shenoy21, Aleksandra Petrovic4, Kirk R Schultz12, Gregory A Yanik11, Edmund K Waller22, John E Levine9, James L Ferrara9, Bruce R Blazar23, Amelia Langston22, John T Horan3, Leslie S Kean3.   

Abstract

PURPOSE: Severe (grade 3-4) acute graft-versus-host disease (AGVHD) is a major cause of death after unrelated-donor (URD) hematopoietic cell transplant (HCT), resulting in particularly high mortality after HLA-mismatched transplantation. There are no approved agents for AGVHD prevention, underscoring the critical unmet need for novel therapeutics. ABA2 was a phase II trial to rigorously assess safety, efficacy, and immunologic effects of adding T-cell costimulation blockade with abatacept to calcineurin inhibitor (CNI)/methotrexate (MTX)-based GVHD prophylaxis, to test whether abatacept could decrease AGVHD.
METHODS: ABA2 enrolled adults and children with hematologic malignancies under two strata: a randomized, double-blind, placebo-controlled stratum (8/8-HLA-matched URD), comparing CNI/MTX plus abatacept with CNI/MTX plus placebo, and a single-arm stratum (7/8-HLA-mismatched URD) comparing CNI/MTX plus abatacept versus CNI/MTX CIBMTR controls. The primary end point was day +100 grade 3-4 AGVHD, with day +180 severe-AGVHD-free-survival (SGFS) a key secondary end point. Sample sizes were calculated using a higher type-1 error (0.2) as recommended for phase II trials, and were based on predicting that abatacept would reduce grade 3-4 AGVHD from 20% to 10% (8/8s) and 30% to 10% (7/8s). ABA2 enrolled 142 recipients (8/8s, median follow-up = 716 days) and 43 recipients (7/8s, median follow-up = 708 days).
RESULTS: In 8/8s, grade 3-4 AGVHD was 6.8% (abatacept) versus 14.8% (placebo) (P = .13, hazard ratio = 0.45). SGFS was 93.2% (CNI/MTX plus abatacept) versus 82% (CNI/MTX plus placebo, P = .05). In the smaller 7/8 cohort, grade 3-4 AGVHD was 2.3% (CNI/MTX plus abatacept, intention-to-treat population), which compared favorably with a nonrandomized matched cohort of CNI/MTX (30.2%, P < .001), and the SGFS was better (97.7% v 58.7%, P < .001). Immunologic analysis revealed control of T-cell activation in abatacept-treated patients.
CONCLUSION: Adding abatacept to URD HCT was safe, reduced AGVHD, and improved SGFS. These results suggest that abatacept may substantially improve AGVHD-related transplant outcomes, with a particularly beneficial impact on HLA-mismatched HCT.

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Year:  2021        PMID: 33449816      PMCID: PMC8260909          DOI: 10.1200/JCO.20.01086

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   50.717


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