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Phase I study evaluating the Fc-optimized FLT3 antibody FLYSYN in AML patients with measurable residual disease

BACKGROUND: About half of AML patients achieving complete remission (CR) display measurable residual disease (MRD) and eventually relapse. FLYSYN is an Fc-optimized antibody for eradication of MRD directed to FLT3/CD135, which is abundantly expressed on AML cells. METHODS: This first-in-human, open-...

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Autores principales: Heitmann, Jonas S., Schlenk, Richard F., Dörfel, Daniela, Kayser, Sabine, Döhner, Konstanze, Heuser, Michael, Thol, Felicitas, Kapp-Schwoerer, Silke, Labrenz, Jannik, Edelmann, Dominic, Märklin, Melanie, Vogel, Wichard, Bethge, Wolfgang, Walz, Juliane S., Große-Hovest, Ludger, Steiner, Martin, Jung, Gundram, Salih, Helmut R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433561/
https://www.ncbi.nlm.nih.gov/pubmed/37587502
http://dx.doi.org/10.1186/s13045-023-01490-w
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author Heitmann, Jonas S.
Schlenk, Richard F.
Dörfel, Daniela
Kayser, Sabine
Döhner, Konstanze
Heuser, Michael
Thol, Felicitas
Kapp-Schwoerer, Silke
Labrenz, Jannik
Edelmann, Dominic
Märklin, Melanie
Vogel, Wichard
Bethge, Wolfgang
Walz, Juliane S.
Große-Hovest, Ludger
Steiner, Martin
Jung, Gundram
Salih, Helmut R.
author_facet Heitmann, Jonas S.
Schlenk, Richard F.
Dörfel, Daniela
Kayser, Sabine
Döhner, Konstanze
Heuser, Michael
Thol, Felicitas
Kapp-Schwoerer, Silke
Labrenz, Jannik
Edelmann, Dominic
Märklin, Melanie
Vogel, Wichard
Bethge, Wolfgang
Walz, Juliane S.
Große-Hovest, Ludger
Steiner, Martin
Jung, Gundram
Salih, Helmut R.
author_sort Heitmann, Jonas S.
collection PubMed
description BACKGROUND: About half of AML patients achieving complete remission (CR) display measurable residual disease (MRD) and eventually relapse. FLYSYN is an Fc-optimized antibody for eradication of MRD directed to FLT3/CD135, which is abundantly expressed on AML cells. METHODS: This first-in-human, open-label, single-arm, multicenter trial included AML patients in CR with persisting or increasing MRD and evaluated safety/tolerability, pharmacokinetics and preliminary efficacy of FLYSYN at different dose levels administered intravenously (cohort 1–5: single dose of 0.5 mg/m(2), 1.5 mg/m(2), 5 mg/m(2), 15 mg/m(2), 45 mg/m(2); cohort 6: 15 mg/m(2) on day 1, 15 and 29). Three patients were treated per cohort except for cohorts 4 and 6, which were expanded to nine and ten patients, respectively. Primary objective was safety, and secondary efficacy objective was ≥ 1 log MRD reduction or negativity in bone marrow. RESULTS: Overall, 31 patients were treated, of whom seven patients (22.6%) experienced a transient decrease in neutrophil count (two grade 3, others ≤ grade 2). No infusion-related reaction or dose-limiting toxicity was observed. Adverse events (AEs) were mostly mild to moderate, with the most frequent AEs being hematologic events and laboratory abnormalities. Response per predefined criteria was documented in 35% of patients, and two patients maintained MRD negativity until end of study. Application of 45 mg/m(2) FLYSYN as single or cumulative dose achieved objective responses in 46% of patients, whereas 28% responded at lower doses. CONCLUSIONS: FLYSYN monotherapy is safe and well-tolerated in AML patients with MRD. Early efficacy data are promising and warrant further evaluation in an up-coming phase II trial. Trial registration This clinical is registered on clinicaltrials.gov (NCT02789254). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-023-01490-w.
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spelling pubmed-104335612023-08-18 Phase I study evaluating the Fc-optimized FLT3 antibody FLYSYN in AML patients with measurable residual disease Heitmann, Jonas S. Schlenk, Richard F. Dörfel, Daniela Kayser, Sabine Döhner, Konstanze Heuser, Michael Thol, Felicitas Kapp-Schwoerer, Silke Labrenz, Jannik Edelmann, Dominic Märklin, Melanie Vogel, Wichard Bethge, Wolfgang Walz, Juliane S. Große-Hovest, Ludger Steiner, Martin Jung, Gundram Salih, Helmut R. J Hematol Oncol Research BACKGROUND: About half of AML patients achieving complete remission (CR) display measurable residual disease (MRD) and eventually relapse. FLYSYN is an Fc-optimized antibody for eradication of MRD directed to FLT3/CD135, which is abundantly expressed on AML cells. METHODS: This first-in-human, open-label, single-arm, multicenter trial included AML patients in CR with persisting or increasing MRD and evaluated safety/tolerability, pharmacokinetics and preliminary efficacy of FLYSYN at different dose levels administered intravenously (cohort 1–5: single dose of 0.5 mg/m(2), 1.5 mg/m(2), 5 mg/m(2), 15 mg/m(2), 45 mg/m(2); cohort 6: 15 mg/m(2) on day 1, 15 and 29). Three patients were treated per cohort except for cohorts 4 and 6, which were expanded to nine and ten patients, respectively. Primary objective was safety, and secondary efficacy objective was ≥ 1 log MRD reduction or negativity in bone marrow. RESULTS: Overall, 31 patients were treated, of whom seven patients (22.6%) experienced a transient decrease in neutrophil count (two grade 3, others ≤ grade 2). No infusion-related reaction or dose-limiting toxicity was observed. Adverse events (AEs) were mostly mild to moderate, with the most frequent AEs being hematologic events and laboratory abnormalities. Response per predefined criteria was documented in 35% of patients, and two patients maintained MRD negativity until end of study. Application of 45 mg/m(2) FLYSYN as single or cumulative dose achieved objective responses in 46% of patients, whereas 28% responded at lower doses. CONCLUSIONS: FLYSYN monotherapy is safe and well-tolerated in AML patients with MRD. Early efficacy data are promising and warrant further evaluation in an up-coming phase II trial. Trial registration This clinical is registered on clinicaltrials.gov (NCT02789254). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-023-01490-w. BioMed Central 2023-08-17 /pmc/articles/PMC10433561/ /pubmed/37587502 http://dx.doi.org/10.1186/s13045-023-01490-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Heitmann, Jonas S.
Schlenk, Richard F.
Dörfel, Daniela
Kayser, Sabine
Döhner, Konstanze
Heuser, Michael
Thol, Felicitas
Kapp-Schwoerer, Silke
Labrenz, Jannik
Edelmann, Dominic
Märklin, Melanie
Vogel, Wichard
Bethge, Wolfgang
Walz, Juliane S.
Große-Hovest, Ludger
Steiner, Martin
Jung, Gundram
Salih, Helmut R.
Phase I study evaluating the Fc-optimized FLT3 antibody FLYSYN in AML patients with measurable residual disease
title Phase I study evaluating the Fc-optimized FLT3 antibody FLYSYN in AML patients with measurable residual disease
title_full Phase I study evaluating the Fc-optimized FLT3 antibody FLYSYN in AML patients with measurable residual disease
title_fullStr Phase I study evaluating the Fc-optimized FLT3 antibody FLYSYN in AML patients with measurable residual disease
title_full_unstemmed Phase I study evaluating the Fc-optimized FLT3 antibody FLYSYN in AML patients with measurable residual disease
title_short Phase I study evaluating the Fc-optimized FLT3 antibody FLYSYN in AML patients with measurable residual disease
title_sort phase i study evaluating the fc-optimized flt3 antibody flysyn in aml patients with measurable residual disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433561/
https://www.ncbi.nlm.nih.gov/pubmed/37587502
http://dx.doi.org/10.1186/s13045-023-01490-w
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