Publication:
Optimal Sequencing and Predictive Biomarkers in Patients with Advanced Prostate Cancer.

dc.contributor.authorCattrini, Carlo
dc.contributor.authorEspaña, Rodrigo
dc.contributor.authorMennitto, Alessia
dc.contributor.authorBersanelli, Melissa
dc.contributor.authorCastro, Elena
dc.contributor.authorOlmos, David
dc.contributor.authorLorente, David
dc.contributor.authorGennari, Alessandra
dc.date.accessioned2023-02-09T11:51:40Z
dc.date.available2023-02-09T11:51:40Z
dc.date.issued2021-09-08
dc.description.abstractThe treatment landscape of advanced prostate cancer has completely changed during the last decades. Chemotherapy (docetaxel, cabazitaxel), androgen-receptor signaling inhibitors (ARSi) (abiraterone acetate, enzalutamide), and radium-223 have revolutionized the management of metastatic castration-resistant prostate cancer (mCRPC). Lutetium-177-PSMA-617 is also going to become another treatment option for these patients. In addition, docetaxel, abiraterone acetate, apalutamide, enzalutamide, and radiotherapy to primary tumor have demonstrated the ability to significantly prolong the survival of patients with metastatic hormone-sensitive prostate cancer (mHSPC). Finally, apalutamide, enzalutamide, and darolutamide have recently provided impactful data in patients with nonmetastatic castration-resistant disease (nmCRPC). However, which is the best treatment sequence for patients with advanced prostate cancer? This comprehensive review aims at discussing the available literature data to identify the optimal sequencing approaches in patients with prostate cancer at different disease stages. Our work also highlights the potential impact of predictive biomarkers in treatment sequencing and exploring the role of specific agents (i.e., olaparib, rucaparib, talazoparib, niraparib, and ipatasertib) in biomarker-selected populations of patients with prostate cancer (i.e., those harboring alterations in DNA damage and response genes or PTEN).
dc.identifier.doi10.3390/cancers13184522
dc.identifier.issn2072-6694
dc.identifier.pmcPMC8467385
dc.identifier.pmid34572748
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467385/pdf
dc.identifier.unpaywallURLhttps://www.mdpi.com/2072-6694/13/18/4522/pdf?version=1631101268
dc.identifier.urihttp://hdl.handle.net/10668/18557
dc.issue.number18
dc.journal.titleCancers
dc.journal.titleabbreviationCancers (Basel)
dc.language.isoen
dc.organizationHospital Universitario Virgen de la Victoria
dc.organizationHospital Universitario Regional de Málaga
dc.organizationInstituto de Investigación Biomédica de Málaga-IBIMA
dc.pubmedtypeJournal Article
dc.pubmedtypeReview
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectLuPSMA
dc.subjectPARP inhibitors
dc.subjectandrogen-receptor signaling inhibitors
dc.subjectchemotherapy
dc.subjectipatasertib
dc.subjectmetastatic castration-resistant prostate cancer
dc.subjectmetastatic hormone-naïve prostate cancer
dc.subjectmetastatic hormone-sensitive prostate cancer
dc.subjectnonmetastatic castration-resistant prostate cancer
dc.titleOptimal Sequencing and Predictive Biomarkers in Patients with Advanced Prostate Cancer.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number13
dspace.entity.typePublication

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