Emerging treatment options for prostate cancer.


Journal

Expert review of anticancer therapy
ISSN: 1744-8328
Titre abrégé: Expert Rev Anticancer Ther
Pays: England
ID NLM: 101123358

Informations de publication

Date de publication:
06 2023
Historique:
medline: 25 5 2023
pubmed: 27 4 2023
entrez: 27 4 2023
Statut: ppublish

Résumé

Prostate cancer treatment has rapidly evolved in the past few years. Androgen deprivation therapy has been the backbone of treatment for locally advanced and metastatic prostate cancer, but incremental benefits in survival have been shown by adding androgen-receptor pathway inhibitors (ARPI) across various spectrums of disease state. In addition, docetaxel chemotherapy remains the first-line chemotherapy regimen available with survival benefits shown with triplet therapy in those who are chemotherapy eligible. However, disease progression remains inevitable and novel agents such as radioligand therapy with lutetium have shown improvement in survival. This review discusses the pivotal trials that led to the U.S. FDA approval of agents utilized in metastatic prostate cancer and explores the use of novel agents including prostate-specific membrane antigen-targeting agents, radioligands, cell-based therapy, chimeric antigen receptor T-cell, BiTE, and antibody drug conjugates. Treatment landscape for metastatic castrate-resistant prostate cancer (mCRPC) has evolved beyond additional agents with ARPI and/or docetaxel, including other treatments with sipuleucel-T, radium, cabazitaxel, PARP inhibitors, and lutetium, which have specific indications and roles in sequencing. Novel therapies remain critically needed after progression from lutetium.

Identifiants

pubmed: 37101345
doi: 10.1080/14737140.2023.2208352
pmc: PMC10718079
mid: NIHMS1942075
doi:

Substances chimiques

Docetaxel 15H5577CQD
Androgen Antagonists 0
Androgens 0
Lutetium 5H0DOZ21UJ

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

625-631

Subventions

Organisme : Intramural NIH HHS
ID : ZIA BC012118
Pays : United States

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Auteurs

Mohammad Atiq (M)

Genitourinary Malignancy Branch, National Cancer Institute, Bethesda, MD, USA.

Elias Chandran (E)

Genitourinary Malignancy Branch, National Cancer Institute, Bethesda, MD, USA.

Fatima Karzai (F)

Genitourinary Malignancy Branch, National Cancer Institute, Bethesda, MD, USA.

Ravi A Madan (RA)

Genitourinary Malignancy Branch, National Cancer Institute, Bethesda, MD, USA.

Jeanny B Aragon-Ching (JB)

GU Medical Oncology, Inova Schar Cancer Institute, Fairfax, VA, USA.
Medical Education, University of Virginia, Charlottesville, VA, USA.

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Classifications MeSH