Imatinib plasma levels in patients with gastrointestinal stromal tumour under routine clinical practice conditions

Author:

Del Rosario García Betel1ORCID,Morales Barrios José Alberto1,Jurado Josefina Cruz2,Díaz Ruth Ramos3ORCID,Viña Romero María Micaela4,Padrón Ivette Mourani3ORCID,Nazco Casariego Gloria Julia1,Nicolás Fernando Gutiérrez15

Affiliation:

1. Servicio de Farmacia, Complejo Hospitalario Universitario de Canarias, San Cristóbal de La Laguna, Tenerife, España

2. Servicio de Oncología Médica, Complejo Hospitalario Universitario de Canarias, San Cristóbal de La Laguna, Tenerife, España

3. Fundación Canaria Instituto de Investigación Sanitaria de Canarias (FIISC), San Cristóbal de La Laguna, Tenerife, España

4. Servicio de Farmacia, Complejo Hospitalario Nuestra Señora de la Candelaria, Santa Cruz de Tenerife, España

5. Unidad de Investigación del Complejo Hospitalario Universitario de Canarias, San Cristóbal de La Laguna, Tenerife, España

Abstract

Objectives Imatinib is the first therapeutic option for the treatment of unresectable or metastatic gastrointestinal stromal tumours. Previous studies have shown an improvement in patient survival rates following the use of imatinib. Nevertheless, adequate plasma concentrations of imatinib are necessary to achieve such improvement in survival and limit the toxicity of the drug. This study aims to analyse the influence of imatinib plasma concentrations on efficacy and safety in the treatment of gastrointestinal stromal tumour. Materials and methods This descriptive, multicentre study analysed plasma levels of imatinib in patients diagnosed with gastrointestinal stromal tumour in the period 2019–2020. An optimal therapeutic range of 750–1500 ng/mL was established for the patient stratification based on their minimum plasma concentrations measured at the steady state. Results This study included 11 patients with metastatic disease in total, among whom only 54.5% (n  =  6) had a minimum plasma concentrations measured at the steady state value within the therapeutic range. A median progression-free survival of 7.0 months was recorded for those patients with minimum plasma concentrations measured at the steady state < 750 ng/mL, while that median progression-free survival value remained unachieved for the group with minimum plasma concentrations measured at the steady state > 750 ng/mL ( p   =   0.005). The toxicity rate was 25% and 14.3% for patients with minimum plasma concentrations measured at the steady state > 1500 ng/mL and minimum plasma concentrations measured at the steady state ≤1500 ng/mL, respectively ( p  =  0.66). Conclusions The present study aims to describe the correlation between the toxicity and effectiveness of imatinib as a function of minimum plasma concentrations measured at the steady state under routine clinical practice conditions. The results described here show the usefulness of imatinib plasma concentrations monitoring as part of the standard daily routine in our hospitals.

Publisher

SAGE Publications

Subject

Pharmacology (medical),Oncology

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