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Cabazitaxel multiple rechallenges in metastatic castration‐resistant prostate cancer
INTRODUCTION: Cabazitaxel multiple rechallenges may be a treatment option in heavily pretreated patients with metastatic castration‐resistant prostate cancer (mCRPC) who had a good initial response to cabazitaxel and who are still fit to receive it. Our objective was to assess the efficacy and toxic...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446560/ https://www.ncbi.nlm.nih.gov/pubmed/34382352 http://dx.doi.org/10.1002/cam4.4172 |
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author | Pobel, Cedric Auclin, Edouard Teyssonneau, Diego Laguerre, Brigitte Cancel, Mathilde Boughalem, Elouen Noel, Johanna Brachet, Pierre Emmanuel Maillet, Denis Barthelemy, Philippe Helissey, Carole Thibault, Constance Oudard, Stéphane |
author_facet | Pobel, Cedric Auclin, Edouard Teyssonneau, Diego Laguerre, Brigitte Cancel, Mathilde Boughalem, Elouen Noel, Johanna Brachet, Pierre Emmanuel Maillet, Denis Barthelemy, Philippe Helissey, Carole Thibault, Constance Oudard, Stéphane |
author_sort | Pobel, Cedric |
collection | PubMed |
description | INTRODUCTION: Cabazitaxel multiple rechallenges may be a treatment option in heavily pretreated patients with metastatic castration‐resistant prostate cancer (mCRPC) who had a good initial response to cabazitaxel and who are still fit to receive it. Our objective was to assess the efficacy and toxicity of multiple rechallenges. PATIENTS AND METHODS: We retrospectively identified 22 mCRPC patients previously treated with docetaxel and/or androgen receptor‐targeted agents who received multiple cabazitaxel rechallenges in 9 French centers. Cabazitaxel was initiated at a dose of 25 mg/m(2) q3week. A reduced dose (20 mg/m(2) q3w) or an alternative schedule (mainly 16 mg/m(2) q2w) was increasingly used for subsequent rechallenges. Progression‐free survival, prostate‐specific antigen (PSA) response, best clinical response, and grade ≥3 toxicities were collected. Overall survival was calculated from various time points. RESULTS: Twenty‐two patients with an initial response to cabazitaxel were rechallenged at least twice. The median number of cabazitaxel cycles was 7 at first cabazitaxel treatment, 6 at first rechallenge, and 5 at subsequent rechallenges. Median progression‐free survival at first rechallenge was 9.6 months and 5.6 months at second rechallenge. Median overall survival was 50.9 months from the first cabazitaxel dose, 114.9 months from first life‐extending therapy initiation in mCRPC, and 105 months from mCRPC diagnosis. There was no cumulative grade ≥3 neuropathy or nail disorder and one case of febrile neutropenia. CONCLUSION: Cabazitaxel multiple rechallenges may be a treatment option without cumulative toxicity in heavily pretreated patients having a good response to first cabazitaxel use and still fit to receive it. NOVELTY & IMPACT STATEMENTS: Patients with metastatic castration‐resistant prostate cancer can be treated with Cabazitaxel after docetaxel and androgen receptor‐targeted agent. This chemotherapy can be used multiple times with efficacy and manageable toxicity. |
format | Online Article Text |
id | pubmed-8446560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84465602021-09-22 Cabazitaxel multiple rechallenges in metastatic castration‐resistant prostate cancer Pobel, Cedric Auclin, Edouard Teyssonneau, Diego Laguerre, Brigitte Cancel, Mathilde Boughalem, Elouen Noel, Johanna Brachet, Pierre Emmanuel Maillet, Denis Barthelemy, Philippe Helissey, Carole Thibault, Constance Oudard, Stéphane Cancer Med Clinical Cancer Research INTRODUCTION: Cabazitaxel multiple rechallenges may be a treatment option in heavily pretreated patients with metastatic castration‐resistant prostate cancer (mCRPC) who had a good initial response to cabazitaxel and who are still fit to receive it. Our objective was to assess the efficacy and toxicity of multiple rechallenges. PATIENTS AND METHODS: We retrospectively identified 22 mCRPC patients previously treated with docetaxel and/or androgen receptor‐targeted agents who received multiple cabazitaxel rechallenges in 9 French centers. Cabazitaxel was initiated at a dose of 25 mg/m(2) q3week. A reduced dose (20 mg/m(2) q3w) or an alternative schedule (mainly 16 mg/m(2) q2w) was increasingly used for subsequent rechallenges. Progression‐free survival, prostate‐specific antigen (PSA) response, best clinical response, and grade ≥3 toxicities were collected. Overall survival was calculated from various time points. RESULTS: Twenty‐two patients with an initial response to cabazitaxel were rechallenged at least twice. The median number of cabazitaxel cycles was 7 at first cabazitaxel treatment, 6 at first rechallenge, and 5 at subsequent rechallenges. Median progression‐free survival at first rechallenge was 9.6 months and 5.6 months at second rechallenge. Median overall survival was 50.9 months from the first cabazitaxel dose, 114.9 months from first life‐extending therapy initiation in mCRPC, and 105 months from mCRPC diagnosis. There was no cumulative grade ≥3 neuropathy or nail disorder and one case of febrile neutropenia. CONCLUSION: Cabazitaxel multiple rechallenges may be a treatment option without cumulative toxicity in heavily pretreated patients having a good response to first cabazitaxel use and still fit to receive it. NOVELTY & IMPACT STATEMENTS: Patients with metastatic castration‐resistant prostate cancer can be treated with Cabazitaxel after docetaxel and androgen receptor‐targeted agent. This chemotherapy can be used multiple times with efficacy and manageable toxicity. John Wiley and Sons Inc. 2021-08-12 /pmc/articles/PMC8446560/ /pubmed/34382352 http://dx.doi.org/10.1002/cam4.4172 Text en © 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Cancer Research Pobel, Cedric Auclin, Edouard Teyssonneau, Diego Laguerre, Brigitte Cancel, Mathilde Boughalem, Elouen Noel, Johanna Brachet, Pierre Emmanuel Maillet, Denis Barthelemy, Philippe Helissey, Carole Thibault, Constance Oudard, Stéphane Cabazitaxel multiple rechallenges in metastatic castration‐resistant prostate cancer |
title | Cabazitaxel multiple rechallenges in metastatic castration‐resistant prostate cancer |
title_full | Cabazitaxel multiple rechallenges in metastatic castration‐resistant prostate cancer |
title_fullStr | Cabazitaxel multiple rechallenges in metastatic castration‐resistant prostate cancer |
title_full_unstemmed | Cabazitaxel multiple rechallenges in metastatic castration‐resistant prostate cancer |
title_short | Cabazitaxel multiple rechallenges in metastatic castration‐resistant prostate cancer |
title_sort | cabazitaxel multiple rechallenges in metastatic castration‐resistant prostate cancer |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446560/ https://www.ncbi.nlm.nih.gov/pubmed/34382352 http://dx.doi.org/10.1002/cam4.4172 |
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