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Flotetuzumab as salvage immunotherapy for refractory acute myeloid leukemia.


ABSTRACT: Approximately 50% of acute myeloid leukemia (AML) patients do not respond to induction therapy (primary induction failure [PIF]) or relapse after <6 months (early relapse [ER]). We have recently shown an association between an immune-infiltrated tumor microenvironment (TME) and resistance to cytarabine-based chemotherapy but responsiveness to flotetuzumab, a bispecific DART antibody-based molecule to CD3ε and CD123. This paper reports the results of a multicenter, open-label, phase 1/2 study of flotetuzumab in 88 adults with relapsed/refractory AML: 42 in a dose-finding segment and 46 at the recommended phase 2 dose (RP2D) of 500 ng/kg per day. The most frequent adverse events were infusion-related reactions (IRRs)/cytokine release syndrome (CRS), largely grade 1-2. Stepwise dosing during week 1, pretreatment dexamethasone, prompt use of tocilizumab, and temporary dose reductions/interruptions successfully prevented severe IRR/CRS. Clinical benefit accrued to PIF/ER patients showing an immune-infiltrated TME. Among 30 PIF/ER patients treated at the RP2D, the complete remission (CR)/CR with partial hematological recovery (CRh) rate was 26.7%, with an overall response rate (CR/CRh/CR with incomplete hematological recovery) of 30.0%. In PIF/ER patients who achieved CR/CRh, median overall survival was 10.2 months (range, 1.87-27.27), with 6- and 12-month survival rates of 75% (95% confidence interval [CI], 0.450-1.05) and 50% (95% CI, 0.154-0.846). Bone marrow transcriptomic analysis showed that a parsimonious 10-gene signature predicted CRs to flotetuzumab (area under the receiver operating characteristic curve = 0.904 vs 0.672 for the European LeukemiaNet classifier). Flotetuzumab represents an innovative experimental approach associated with acceptable safety and encouraging evidence of activity in PIF/ER patients. This trial was registered at www.clinicaltrials.gov as #NCT02152956.

SUBMITTER: Uy GL 

PROVIDER: S-EPMC7885824 | biostudies-literature | 2021 Feb

REPOSITORIES: biostudies-literature

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Flotetuzumab as salvage immunotherapy for refractory acute myeloid leukemia.

Uy Geoffrey L GL   Aldoss Ibrahim I   Foster Matthew C MC   Sayre Peter H PH   Wieduwilt Matthew J MJ   Advani Anjali S AS   Godwin John E JE   Arellano Martha L ML   Sweet Kendra L KL   Emadi Ashkan A   Ravandi Farhad F   Erba Harry P HP   Byrne Michael M   Michaelis Laura L   Topp Max S MS   Vey Norbert N   Ciceri Fabio F   Carrabba Matteo Giovanni MG   Paolini Stefania S   Huls Gerwin A GA   Jongen-Lavrencic Mojca M   Wermke Martin M   Chevallier Patrice P   Gyan Emmanuel E   Récher Christian C   Stiff Patrick J PJ   Pettit Kristen M KM   Löwenberg Bob B   Church Sarah E SE   Anderson Erica E   Vadakekolathu Jayakumar J   Santaguida Marianne M   Rettig Michael P MP   Muth John J   Curtis Teia T   Fehr Erin E   Guo Kuo K   Zhao Jian J   Bakkacha Ouiam O   Jacobs Kenneth K   Tran Kathy K   Kaminker Patrick P   Kostova Maya M   Bonvini Ezio E   Walter Roland B RB   Davidson-Moncada Jan K JK   Rutella Sergio S   DiPersio John F JF  

Blood 20210201 6


Approximately 50% of acute myeloid leukemia (AML) patients do not respond to induction therapy (primary induction failure [PIF]) or relapse after <6 months (early relapse [ER]). We have recently shown an association between an immune-infiltrated tumor microenvironment (TME) and resistance to cytarabine-based chemotherapy but responsiveness to flotetuzumab, a bispecific DART antibody-based molecule to CD3ε and CD123. This paper reports the results of a multicenter, open-label, phase 1/2 study of  ...[more]

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