Neutropenia, neutrophilia, and neutrophil-lymphocyte ratio as prognostic markers in patients with metastatic castration-resistant prostate cancer.
cabazitaxel
mCRPC
neutropenia
neutrophil-to-lymphocyte ratio
neutrophilia
prostate cancer
Journal
Therapeutic advances in medical oncology
ISSN: 1758-8340
Titre abrégé: Ther Adv Med Oncol
Pays: England
ID NLM: 101510808
Informations de publication
Date de publication:
2022
2022
Historique:
received:
07
12
2021
accepted:
25
04
2022
entrez:
9
6
2022
pubmed:
10
6
2022
medline:
10
6
2022
Statut:
epublish
Résumé
Chemotherapy-induced neutropenia and neutrophil-to-lymphocyte ratio (NLR) are potentially useful prognostic markers in patients with metastatic castration-resistant prostate cancer (mCRPC). This post hoc analysis investigated whether these markers can be utilized for dose considerations and evaluated the prognostic impact of leukocyte subtypes. PROSELICA assessed the non-inferiority of cabazitaxel 20 mg/m PROSELICA confirmed the negative prognostic value of increased baseline NLR [⩾3, hazard ratio (HR) 1.40; Grade ⩾ 3 neutropenia was the only leukocyte-based biomarker associated with all key outcome parameters in mCRPC patients receiving cabazitaxel and might be able to overcome the negative prognostic effect of baseline neutrophilia. NCT01308580.
Sections du résumé
Background and purpose
UNASSIGNED
Chemotherapy-induced neutropenia and neutrophil-to-lymphocyte ratio (NLR) are potentially useful prognostic markers in patients with metastatic castration-resistant prostate cancer (mCRPC). This post hoc analysis investigated whether these markers can be utilized for dose considerations and evaluated the prognostic impact of leukocyte subtypes.
Patients and methods
UNASSIGNED
PROSELICA assessed the non-inferiority of cabazitaxel 20 mg/m
Results
UNASSIGNED
PROSELICA confirmed the negative prognostic value of increased baseline NLR [⩾3, hazard ratio (HR) 1.40;
Conclusions
UNASSIGNED
Grade ⩾ 3 neutropenia was the only leukocyte-based biomarker associated with all key outcome parameters in mCRPC patients receiving cabazitaxel and might be able to overcome the negative prognostic effect of baseline neutrophilia.
NCT number
UNASSIGNED
NCT01308580.
Identifiants
pubmed: 35677318
doi: 10.1177/17588359221100022
pii: 10.1177_17588359221100022
pmc: PMC9168856
doi:
Banques de données
ClinicalTrials.gov
['NCT01308580']
Types de publication
Journal Article
Langues
eng
Pagination
17588359221100022Subventions
Organisme : Medical Research Council
ID : MR/W018217/1
Pays : United Kingdom
Informations de copyright
© The Author(s), 2022.
Déclaration de conflit d'intérêts
Conflict of interest statement: The authors declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: AM has provided a consulting, advisory or speaker role for Amgen, Astellas, Boehringer Ingelheim, Celgene, Janssen, Gerresheimer, Glaxo-Smith-Kline, Merck, MSD, Novartis, Roche, Sanofi, Servier, Takeda, and Vifor, has received research funding from Bayer (personal) and Merck & Cie (institutional), has intellectual property interests relating to Merck (not related to this report), has been paid to provide expert testimony for Sanofi, and has reported travel/accommodation expenses paid for by Amgen, Astellas, Boehringer Ingelheim, Janssen, Merck, Roche, Sanofi, and Servier. RdW has provided a consulting or advisory role for Sanofi, Merck Sharp & Dohme, Roche/Genetech, Janssen, Bayer and Clovis Oncology. RdW has also received honoraria and/or research funding from Sanofi and Bayer. SO has provided a consulting or advisory role for AstraZeneca, Sanofi, Roche/Genetech, Janssen, Bayer and Astellas, Pfizer, Merck Sharp & Dohme, Novartis, Bristol Myers Squib. SO has also received honoraria and/or research funding from Sanofi, AstraZeneca, Bayer, Pfizer, Janssen, and Bristol Myers Squib. OS has provided a consulting role for Advanced Accelerator Applications (AAA), Astellas, AstraZeneca, Bayer, Blue Earth Diagnostics, Inc., Bavarian Nordic, Bristol Myers Squibb, Clarity Pharmaceuticals, Clovis, Constellation, Dendreon, EMD Serono, Fusion, Isotopen Technologien Meunchen, Janssen, Merck, Moyvant, Myriad, Noria Therapeutics, Inc., Novartis, Noxopharm, Progenics, POINT Biopharma, Pfizer, Sanofi, Tenebio, Telix, Theragnostics. OS has received grant/research support from Advanced Accelerator Applications, Amgen, AstraZeneca, Bayer, Constellation, Endocyte, Invitae, Janssen, Lantheus, Merck, Progenics, and Tenebio. FS-L has provided a consulting or advisory role for Bayer, BMS, Janssen, MSD, AstraZeneca and Sanofi. FS-L has also reported travel/other expenses from BMS, Sanofi, and Roche. ZS was an employee of Sanofi. MF and AO are current/former Sanofi employees. AO owns stocks in Sanofi. ME is on the board of directors for VERU Inc. JSdB has provided a consulting or advisory role for AstraZeneca, Sanofi, Roche, Astellas Pharma, Bayer, Pfizer, Merck Sharp & Dohme, Merck Serono, Boehringer Ingelheim, Sierra Oncology, Menarini Silicon Biostystems, Celgene, Taiho Pharmaceuticals, Daiichi Sankyo, Janssen, Genmab, GSK, Orion Pharma GmbH, Eisai, and BioXCel therapeutics, and received travel/accommodation/expenses from AstraZeneca, Astellas Pharma, GSK, Orion Pharma GmbH, Sanofi, Genmab, Taiho Pharmaceuticals, Qiagen, and Vertex. JSdB is also associated with patents/royalties/other IP for abiraterone, PARP inhibitors, IL-23 targeting in prostate cancer, CHK1 inhibitor. JSdB has also received honoraria and/or research funding from AstraZeneca, Sanofi, Astellas Pharma, Pfizer, Roche/Genentech, Janssen, Menarini Silicon Biosystems, Daiichi Sankyo, Sierra Oncology, Taiho Pharmaceuticals, Merck Serono, Astex Pharmaceuticals, Merck Sharp & Dohme, Orion Pharma GmbH, CellCentric, Celgene, Bayer, MedImmune, Medivation, and BioExcel.
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