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Comparative assessment of pharmacokinetics, and pharmacodynamics between RTXM83™, a rituximab biosimilar, and rituximab in diffuse large B-cell lymphoma patients: a population PK model approach.
Candelaria, Myrna; Gonzalez, Derlis; Fernández Gómez, Francisco Javier; Paravisini, Alexandra; Del Campo García, Ana; Pérez, Luis; Miguel-Lillo, Bernardo; Millán, Susana.
Afiliação
  • Candelaria M; Instituto Nacional de Cancerología, Av. San Fernando No. 22, Tlalpan, Sección XVI, Mexico, DF, Mexico.
  • Gonzalez D; Instituto Privado de Hematología e Investigación Clínica (IPHIC), Mariano Roque Alonso 1450, Asunción, Paraguay.
  • Fernández Gómez FJ; mAbxience Research S.L., Manuel Pombo Angulo 28, 28050, Madrid, Spain. javierfergo@outlook.com.
  • Paravisini A; mAbxience Research S.L., Manuel Pombo Angulo 28, 28050, Madrid, Spain.
  • Del Campo García A; mAbxience Research S.L., Manuel Pombo Angulo 28, 28050, Madrid, Spain.
  • Pérez L; mAbxience Research S.L., Manuel Pombo Angulo 28, 28050, Madrid, Spain.
  • Miguel-Lillo B; SGS Exprimo NV, Mechelen, Belgium.
  • Millán S; mAbxience Research S.L., Manuel Pombo Angulo 28, 28050, Madrid, Spain.
Cancer Chemother Pharmacol ; 81(3): 515-527, 2018 03.
Article em En | MEDLINE | ID: mdl-29362903
PURPOSE: The main objective was to quantify any potential differences in pharmacokinetic (PK) parameters (AUC and Cmax) between RTXM83, a proposed rituximab biosimilar, and its reference product, using a population PK model approach. METHODS: Rituximab PK and PD data were obtained from a randomized, double-blind, phase III clinical study (RTXM83-AC-01-11) in patients with diffuse large B-cell lymphoma (DLBCL) that received 375 mg/m2 intravenous RTXM83 or its reference product with CHOP regimen, every 3 weeks, for six cycles. Rituximab levels were quantified by Meso Scale Discovery assay. PK analysis was performed using NONMEM 7.3.0. The effect of disease and patient covariates on RXTM83 PK was investigated. Model was evaluated using visual predictive check and non-parametric bootstrap. RESULTS: In total, 251 DLBCL patients (127 and 124 in RXTM83-CHOP and rituximab-CHOP arms, respectively) and 5341 serum concentrations (2703 for RXTM83 and 2638 for rituximab, respectively) were available for the population PK analysis. The volume of distribution of the central compartment (V1) and clearance of RXTM83 were estimated at 3.19 L and 12.5 mL/h, respectively. Body surface area allowed to explain the interindividual variability for V1. A statistical analysis showed that systemic exposure (AUC and Cmax) of RTXM83 was similar to rituximab. The 90% confidence intervals for all pairwise comparisons were within the predefined bioequivalence interval of 0.80-1.25. PD similarity of B-cell depletion and recovery was also observed. CONCLUSIONS: The time course of RTXM83 was well characterized by the model developed. The systemic exposure of RTXM83 and its associated variability were similar to those for rituximab reference in DLBCL patients, demonstrating PK similarity. The PD similarity of RTXM83 and rituximab reference product was also demonstrated.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma Difuso de Grandes Células B / Medicamentos Biossimilares / Rituximab Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Cancer Chemother Pharmacol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: México País de publicação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma Difuso de Grandes Células B / Medicamentos Biossimilares / Rituximab Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Cancer Chemother Pharmacol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: México País de publicação: Alemanha