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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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