Cargando…

Preclinical profile of cabazitaxel

First-generation taxanes have changed the treatment paradigm for a wide variety of cancers, but innate or acquired resistance frequently limits their use. Cabazitaxel is a novel second-generation taxane developed to overcome such resistance. In vitro, cabazitaxel showed similar antiproliferative act...

Descripción completa

Detalles Bibliográficos
Autores principales: Vrignaud, Patricia, Semiond, Dorothée, Benning, Veronique, Beys, Eric, Bouchard, Hervé, Gupta, Sunil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207555/
https://www.ncbi.nlm.nih.gov/pubmed/25378905
http://dx.doi.org/10.2147/DDDT.S64940
_version_ 1782340989324623872
author Vrignaud, Patricia
Semiond, Dorothée
Benning, Veronique
Beys, Eric
Bouchard, Hervé
Gupta, Sunil
author_facet Vrignaud, Patricia
Semiond, Dorothée
Benning, Veronique
Beys, Eric
Bouchard, Hervé
Gupta, Sunil
author_sort Vrignaud, Patricia
collection PubMed
description First-generation taxanes have changed the treatment paradigm for a wide variety of cancers, but innate or acquired resistance frequently limits their use. Cabazitaxel is a novel second-generation taxane developed to overcome such resistance. In vitro, cabazitaxel showed similar antiproliferative activity to docetaxel in taxane-sensitive cell lines and markedly greater activity in cell lines resistant to taxanes. In vivo, cabazitaxel demonstrated excellent antitumor activity in a broad spectrum of docetaxel-sensitive tumor xenografts, including a castration-resistant prostate tumor xenograft, HID28, where cabazitaxel exhibited greater efficacy than docetaxel. Importantly, cabazitaxel was also active against tumors with innate or acquired resistance to docetaxel, suggesting therapeutic potential for patients progressing following taxane treatment and those with docetaxel-refractory tumors. In patients with tumors of the central nervous system (CNS), and in patients with pediatric tumors, therapeutic success with first-generation taxanes has been limited. Cabazitaxel demonstrated greater antitumor activity than docetaxel in xenograft models of CNS disease and pediatric tumors, suggesting potential clinical utility in these special patient populations. Based on therapeutic synergism observed in an in vivo tumor model, cabazitaxel is also being investigated clinically in combination with cisplatin. Nonclinical evaluation of the safety of cabazitaxel in a range of animal species showed largely reversible changes in the bone marrow, lymphoid system, gastrointestinal tract, and male reproductive system. Preclinical safety signals of cabazitaxel were consistent with the previously reported safety profiles of paclitaxel and docetaxel. Clinical observations with cabazitaxel were consistent with preclinical results, and cabazitaxel is indicated, in combination with prednisone, for the treatment of patients with hormone-refractory metastatic prostate cancer previously treated with docetaxel. In conclusion, the demonstrated activity of cabazitaxel in tumors with innate or acquired resistance to docetaxel, CNS tumors, and pediatric tumors made this agent a candidate for further clinical evaluation in a broader range of patient populations compared with first-generation taxanes.
format Online
Article
Text
id pubmed-4207555
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-42075552014-11-06 Preclinical profile of cabazitaxel Vrignaud, Patricia Semiond, Dorothée Benning, Veronique Beys, Eric Bouchard, Hervé Gupta, Sunil Drug Des Devel Ther Review First-generation taxanes have changed the treatment paradigm for a wide variety of cancers, but innate or acquired resistance frequently limits their use. Cabazitaxel is a novel second-generation taxane developed to overcome such resistance. In vitro, cabazitaxel showed similar antiproliferative activity to docetaxel in taxane-sensitive cell lines and markedly greater activity in cell lines resistant to taxanes. In vivo, cabazitaxel demonstrated excellent antitumor activity in a broad spectrum of docetaxel-sensitive tumor xenografts, including a castration-resistant prostate tumor xenograft, HID28, where cabazitaxel exhibited greater efficacy than docetaxel. Importantly, cabazitaxel was also active against tumors with innate or acquired resistance to docetaxel, suggesting therapeutic potential for patients progressing following taxane treatment and those with docetaxel-refractory tumors. In patients with tumors of the central nervous system (CNS), and in patients with pediatric tumors, therapeutic success with first-generation taxanes has been limited. Cabazitaxel demonstrated greater antitumor activity than docetaxel in xenograft models of CNS disease and pediatric tumors, suggesting potential clinical utility in these special patient populations. Based on therapeutic synergism observed in an in vivo tumor model, cabazitaxel is also being investigated clinically in combination with cisplatin. Nonclinical evaluation of the safety of cabazitaxel in a range of animal species showed largely reversible changes in the bone marrow, lymphoid system, gastrointestinal tract, and male reproductive system. Preclinical safety signals of cabazitaxel were consistent with the previously reported safety profiles of paclitaxel and docetaxel. Clinical observations with cabazitaxel were consistent with preclinical results, and cabazitaxel is indicated, in combination with prednisone, for the treatment of patients with hormone-refractory metastatic prostate cancer previously treated with docetaxel. In conclusion, the demonstrated activity of cabazitaxel in tumors with innate or acquired resistance to docetaxel, CNS tumors, and pediatric tumors made this agent a candidate for further clinical evaluation in a broader range of patient populations compared with first-generation taxanes. Dove Medical Press 2014-10-13 /pmc/articles/PMC4207555/ /pubmed/25378905 http://dx.doi.org/10.2147/DDDT.S64940 Text en © 2014 Vrignaud et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Vrignaud, Patricia
Semiond, Dorothée
Benning, Veronique
Beys, Eric
Bouchard, Hervé
Gupta, Sunil
Preclinical profile of cabazitaxel
title Preclinical profile of cabazitaxel
title_full Preclinical profile of cabazitaxel
title_fullStr Preclinical profile of cabazitaxel
title_full_unstemmed Preclinical profile of cabazitaxel
title_short Preclinical profile of cabazitaxel
title_sort preclinical profile of cabazitaxel
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207555/
https://www.ncbi.nlm.nih.gov/pubmed/25378905
http://dx.doi.org/10.2147/DDDT.S64940
work_keys_str_mv AT vrignaudpatricia preclinicalprofileofcabazitaxel
AT semionddorothee preclinicalprofileofcabazitaxel
AT benningveronique preclinicalprofileofcabazitaxel
AT beyseric preclinicalprofileofcabazitaxel
AT bouchardherve preclinicalprofileofcabazitaxel
AT guptasunil preclinicalprofileofcabazitaxel