A pharmacometrics model to define docetaxel target in early breast cancer
- Autores
- Aldaz, Azucena; Schaiquevich, Paula Susana; Aramendía, José Manuel
- Año de publicación
- 2022
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Aims: We aimed to study the relation between pharmacokinetics (PK) and pharmacodynamics (PD) of docetaxel in early breast cancer and recommend a target exposure. Methods: A PK/PD study was performed in 27 early breast cancer patients treated with doxorubicin and cyclophosphamide for 4 cycles followed by 4 cycles of docetaxel 75–100 mg/m2 infused every 21 days. Individual Bayesian estimates of docetaxel PK parameters were obtained using a nonparametric population PK model developed with data from patients with metastatic breast cancer who received dose-intensified docetaxel (300–350 mg/m2). Docetaxel area under the curve (AUC) and maximum concentration (Cmax) in each cycle and total cumulative AUC (AUCcum) were calculated and related to the incidence of adverse effects and tumour recurrence. Results: Docetaxel clearance showed no change over the 4 treatment cycles, but a gradual increase in the volume of distribution was observed. One third of the patients had at least 1 dose reduction of docetaxel due to toxicity. The mean AUC, AUCcum and Cmax in patients showing docetaxel-associated adverse events were significantly higher than in patients free of toxicity (P <.05). Fatigue and decrease in haemoglobin and haematocrit levels were related to docetaxel AUC and Cmax and pain to AUC. AUC and Cmax >4.5 mg*h/L and 3.5 mg/L, respectively, were risk factors for docetaxel toxicity, while an AUC <4.5 mg*h/L was associated with tumour recurrence. Conclusion: We report for the first time a relation between docetaxel exposure and toxicity and recommend specific targets of drug exposure with implications for the clinical management of early breast cancer patients.
Fil: Aldaz, Azucena. Universidad de Navarra; España
Fil: Schaiquevich, Paula Susana. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Aramendía, José Manuel. Universidad de Navarra; España - Materia
-
BREAST CANCER
DOCETAXEL
PHARMACODYNAMICS
PHARMACOKINETICS
PRECISION MEDICINE - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/200647
Ver los metadatos del registro completo
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A pharmacometrics model to define docetaxel target in early breast cancerAldaz, AzucenaSchaiquevich, Paula SusanaAramendía, José ManuelBREAST CANCERDOCETAXELPHARMACODYNAMICSPHARMACOKINETICSPRECISION MEDICINEhttps://purl.org/becyt/ford/3.2https://purl.org/becyt/ford/3Aims: We aimed to study the relation between pharmacokinetics (PK) and pharmacodynamics (PD) of docetaxel in early breast cancer and recommend a target exposure. Methods: A PK/PD study was performed in 27 early breast cancer patients treated with doxorubicin and cyclophosphamide for 4 cycles followed by 4 cycles of docetaxel 75–100 mg/m2 infused every 21 days. Individual Bayesian estimates of docetaxel PK parameters were obtained using a nonparametric population PK model developed with data from patients with metastatic breast cancer who received dose-intensified docetaxel (300–350 mg/m2). Docetaxel area under the curve (AUC) and maximum concentration (Cmax) in each cycle and total cumulative AUC (AUCcum) were calculated and related to the incidence of adverse effects and tumour recurrence. Results: Docetaxel clearance showed no change over the 4 treatment cycles, but a gradual increase in the volume of distribution was observed. One third of the patients had at least 1 dose reduction of docetaxel due to toxicity. The mean AUC, AUCcum and Cmax in patients showing docetaxel-associated adverse events were significantly higher than in patients free of toxicity (P <.05). Fatigue and decrease in haemoglobin and haematocrit levels were related to docetaxel AUC and Cmax and pain to AUC. AUC and Cmax >4.5 mg*h/L and 3.5 mg/L, respectively, were risk factors for docetaxel toxicity, while an AUC <4.5 mg*h/L was associated with tumour recurrence. Conclusion: We report for the first time a relation between docetaxel exposure and toxicity and recommend specific targets of drug exposure with implications for the clinical management of early breast cancer patients.Fil: Aldaz, Azucena. Universidad de Navarra; EspañaFil: Schaiquevich, Paula Susana. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Aramendía, José Manuel. Universidad de Navarra; EspañaWiley Blackwell Publishing, Inc2022-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/200647Aldaz, Azucena; Schaiquevich, Paula Susana; Aramendía, José Manuel; A pharmacometrics model to define docetaxel target in early breast cancer; Wiley Blackwell Publishing, Inc; British Journal Of Clinical Pharmacology; 89; 2; 9-2022; 727-7360306-5251CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1111/bcp.15526info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T11:02:48Zoai:ri.conicet.gov.ar:11336/200647instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 11:02:49.031CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
A pharmacometrics model to define docetaxel target in early breast cancer |
| title |
A pharmacometrics model to define docetaxel target in early breast cancer |
| spellingShingle |
A pharmacometrics model to define docetaxel target in early breast cancer Aldaz, Azucena BREAST CANCER DOCETAXEL PHARMACODYNAMICS PHARMACOKINETICS PRECISION MEDICINE |
| title_short |
A pharmacometrics model to define docetaxel target in early breast cancer |
| title_full |
A pharmacometrics model to define docetaxel target in early breast cancer |
| title_fullStr |
A pharmacometrics model to define docetaxel target in early breast cancer |
| title_full_unstemmed |
A pharmacometrics model to define docetaxel target in early breast cancer |
| title_sort |
A pharmacometrics model to define docetaxel target in early breast cancer |
| dc.creator.none.fl_str_mv |
Aldaz, Azucena Schaiquevich, Paula Susana Aramendía, José Manuel |
| author |
Aldaz, Azucena |
| author_facet |
Aldaz, Azucena Schaiquevich, Paula Susana Aramendía, José Manuel |
| author_role |
author |
| author2 |
Schaiquevich, Paula Susana Aramendía, José Manuel |
| author2_role |
author author |
| dc.subject.none.fl_str_mv |
BREAST CANCER DOCETAXEL PHARMACODYNAMICS PHARMACOKINETICS PRECISION MEDICINE |
| topic |
BREAST CANCER DOCETAXEL PHARMACODYNAMICS PHARMACOKINETICS PRECISION MEDICINE |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.2 https://purl.org/becyt/ford/3 |
| dc.description.none.fl_txt_mv |
Aims: We aimed to study the relation between pharmacokinetics (PK) and pharmacodynamics (PD) of docetaxel in early breast cancer and recommend a target exposure. Methods: A PK/PD study was performed in 27 early breast cancer patients treated with doxorubicin and cyclophosphamide for 4 cycles followed by 4 cycles of docetaxel 75–100 mg/m2 infused every 21 days. Individual Bayesian estimates of docetaxel PK parameters were obtained using a nonparametric population PK model developed with data from patients with metastatic breast cancer who received dose-intensified docetaxel (300–350 mg/m2). Docetaxel area under the curve (AUC) and maximum concentration (Cmax) in each cycle and total cumulative AUC (AUCcum) were calculated and related to the incidence of adverse effects and tumour recurrence. Results: Docetaxel clearance showed no change over the 4 treatment cycles, but a gradual increase in the volume of distribution was observed. One third of the patients had at least 1 dose reduction of docetaxel due to toxicity. The mean AUC, AUCcum and Cmax in patients showing docetaxel-associated adverse events were significantly higher than in patients free of toxicity (P <.05). Fatigue and decrease in haemoglobin and haematocrit levels were related to docetaxel AUC and Cmax and pain to AUC. AUC and Cmax >4.5 mg*h/L and 3.5 mg/L, respectively, were risk factors for docetaxel toxicity, while an AUC <4.5 mg*h/L was associated with tumour recurrence. Conclusion: We report for the first time a relation between docetaxel exposure and toxicity and recommend specific targets of drug exposure with implications for the clinical management of early breast cancer patients. Fil: Aldaz, Azucena. Universidad de Navarra; España Fil: Schaiquevich, Paula Susana. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Aramendía, José Manuel. Universidad de Navarra; España |
| description |
Aims: We aimed to study the relation between pharmacokinetics (PK) and pharmacodynamics (PD) of docetaxel in early breast cancer and recommend a target exposure. Methods: A PK/PD study was performed in 27 early breast cancer patients treated with doxorubicin and cyclophosphamide for 4 cycles followed by 4 cycles of docetaxel 75–100 mg/m2 infused every 21 days. Individual Bayesian estimates of docetaxel PK parameters were obtained using a nonparametric population PK model developed with data from patients with metastatic breast cancer who received dose-intensified docetaxel (300–350 mg/m2). Docetaxel area under the curve (AUC) and maximum concentration (Cmax) in each cycle and total cumulative AUC (AUCcum) were calculated and related to the incidence of adverse effects and tumour recurrence. Results: Docetaxel clearance showed no change over the 4 treatment cycles, but a gradual increase in the volume of distribution was observed. One third of the patients had at least 1 dose reduction of docetaxel due to toxicity. The mean AUC, AUCcum and Cmax in patients showing docetaxel-associated adverse events were significantly higher than in patients free of toxicity (P <.05). Fatigue and decrease in haemoglobin and haematocrit levels were related to docetaxel AUC and Cmax and pain to AUC. AUC and Cmax >4.5 mg*h/L and 3.5 mg/L, respectively, were risk factors for docetaxel toxicity, while an AUC <4.5 mg*h/L was associated with tumour recurrence. Conclusion: We report for the first time a relation between docetaxel exposure and toxicity and recommend specific targets of drug exposure with implications for the clinical management of early breast cancer patients. |
| publishDate |
2022 |
| dc.date.none.fl_str_mv |
2022-09 |
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http://hdl.handle.net/11336/200647 Aldaz, Azucena; Schaiquevich, Paula Susana; Aramendía, José Manuel; A pharmacometrics model to define docetaxel target in early breast cancer; Wiley Blackwell Publishing, Inc; British Journal Of Clinical Pharmacology; 89; 2; 9-2022; 727-736 0306-5251 CONICET Digital CONICET |
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Aldaz, Azucena; Schaiquevich, Paula Susana; Aramendía, José Manuel; A pharmacometrics model to define docetaxel target in early breast cancer; Wiley Blackwell Publishing, Inc; British Journal Of Clinical Pharmacology; 89; 2; 9-2022; 727-736 0306-5251 CONICET Digital CONICET |
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eng |
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Wiley Blackwell Publishing, Inc |
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reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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