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Population Pharmacokinetics of Inotuzumab Ozogamicin in Pediatric Relapsed/Refractory B-Cell Precursor Acute Lymphoblastic Leukemia: Results of Study ITCC-059.

Jen-Hao Wu ,
Edoardo Pennesi ,
Francisco Bautista ,
May Garrett ,
Kei Fukuhara ,
Erica Brivio ,
Anneke C J Ammerlaan ,
Franco Locatelli ,
Inge M van der Sluis ,
Claudia Rossig ,
Christiane Chen-Santel ,
Bella Bielorai ,
Arnaud Petit ,
Jan Starý ,
Cristina Díaz-de-Heredia ,
Susana Rives ,
Aengus O'Marcaigh ,
Carmelo Rizzari ,
Gernot Engstler ,
Karsten Nysom ,
Alba Rubio-San-Simón ,
Benedicte Bruno ,
Yves Bertrand ,
Benoît Brethon ,
Fanny Rialland ,
Geneviève Plat ,
Uta Dirksen ,
Lucie Sramkova ,
C Michel Zwaan ,
Alwin D R Huitema

Abstract

METHODS

From 531 adult patients with B-cell non-Hodgkin's lymphoma, 234 adult patients with BCP-ALL, and 53 pediatric patients with BCP-ALL, 8924 inotuzumab ozogamicin serum concentrations were analyzed using non-linear mixed-effects modeling. A published adult inotuzumab ozogamicin population-pharmacokinetic model, a two-compartment model with linear and time-dependent clearance, was adapted to describe the pediatric data.

CONCLUSIONS

The pharmacokinetic profile of inotuzumab ozogamicin in pediatric patients with relapsed/refractory BCP-ALL was well described in this study. No dose adjustment is required clinically for pediatric patients with BCP-ALL based on the simulated inotuzumab ozogamicin exposure at the recommended pediatric phase II dose, promising efficacy and acceptable tolerability.

RESULTS

Modifications in this analysis, compared to the published adult model, included: (i) re-estimating pharmacokinetic parameters and covariate effects; (ii) modifying covariate representation; and (iii) introducing relevant pediatric covariate effects (age on the decay coefficient of time-dependent clearance and ALL effect (disease type and/or different bioanalytical analysis methods) on initial values of time-dependent clearance). For patients with relapsed/refractory BCP-ALL, increasing age was associated with a decreasing decay coefficient of time-dependent clearance, reflecting that the target-mediated drug clearance declines more rapidly in children. In pediatric BCP-ALL, the median [interquartile range] cumulative area under the concentration-time curve was significantly higher among responders (n = 42) versus non-responders (n = 10) at the end of the first cycle (26.1 [18.9-35.0] vs 10.1 [9.19-16.1], × 103 ng*h/mL, p < 0.001). From simulations performed at the recommended pediatric phase II dose, inotuzumab ozogamicin exposure reached a similar level as observed in responding pediatric trial participants.

BACKGROUND AND OBJECTIVE

Inotuzumab ozogamicin is an antibody-drug conjugate approved for treating relapsed/refractory B-cell precursor acute lymphoblastic leukemia (BCP-ALL) in adults. Pediatric pharmacokinetic data of inotuzumab ozogamicin are lacking. This study is the first to examine the population pharmacokinetics of inotuzumab ozogamicin in pediatric patients with relapsed/refractory BCP-ALL.

More about this publication

Clinical pharmacokinetics

Volume 63
Issue nr. 7
Pages 981-997
Publication date 01-07-2024

Full text links

Publisher website (DOI) 10.1007/s40262-024-01386-z
Europe PubMed Central 38907948
Pubmed 38907948

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