Beyond the Androgen Receptor: The Sequence, the Mutants, and New Avengers in the Treatment of Castrate-Resistant Metastatic Prostate Cancer.


Journal

American Society of Clinical Oncology educational book. American Society of Clinical Oncology. Annual Meeting
ISSN: 1548-8756
Titre abrégé: Am Soc Clin Oncol Educ Book
Pays: United States
ID NLM: 101233985

Informations de publication

Date de publication:
Jun 2021
Historique:
entrez: 1 6 2021
pubmed: 2 6 2021
medline: 17 11 2021
Statut: ppublish

Résumé

Targeting the androgen receptor by depriving testosterone with gonadotropin-releasing hormone agonists or antagonists, or surgical castration, has been the backbone of metastatic prostate cancer treatment. Although most prostate cancers initially respond to androgen deprivation, metastatic castration-resistant prostate cancer evolves into a heterogeneous disease with diverse drivers of progression and mechanisms of therapeutic resistance. Development of castrate resistance phenotype is associated with lethality despite the recent noteworthy strides gained via increase in therapeutic options. Identification of novel therapeutics to further improve survival and achieve durable responses in metastatic castration-resistant prostate cancer is a clinical necessity. In this review, we outline the existing avengers for treatment of metastatic castration-resistant prostate cancer by clinical presentation, placing into context the clinical state of the patient, such as burden of disease and symptoms. Doing so might aid in the ability to optimize the sequence of agents and allow for maximal exposure to life-prolonging therapeutics. Realizing the limitations of the androgen signaling inhibition, we explore the androgen-indifferent prostate cancer: the mutants. Classically, these subtypes have been associated with variant histology, but androgen-indifferent prostate cancer features are now frequently observed in association with heterogeneous morphologies, including double-negative prostate cancers, lacking both androgen receptor and neuroendocrine features, or clinicopathologic criteria, such as the aggressive variant prostate cancer criteria. The framework of new avengers against metastatic castration-resistant prostate cancer based on mechanism, including DNA repair, immune checkpoint inhibition, PTEN/PI3K/AKT pathway, prostate-specific membrane antigen targets, bispecific T-cell engagers, and radionuclide therapies, is summarized in this review.

Identifiants

pubmed: 34061561
doi: 10.1200/EDBK_321209
doi:

Substances chimiques

Androgen Antagonists 0
Receptors, Androgen 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e190-e202

Auteurs

Daniel Westaby (D)

The Institute of Cancer Research and The Royal Marsden Hospital, London, United Kingdom.

Paul V Viscuse (PV)

Division of Cancer Medicine, University of Texas MD Anderson Cancer Center, Houston, TX.

Rahul Ravilla (R)

US Oncology Research, New York Oncology Hematology, Albany, NY.

Maria de Los Dolores Fenor de la Maza (MLDF)

The Institute of Cancer Research and The Royal Marsden Hospital, London, United Kingdom.

Andrew Hahn (A)

Division of Cancer Medicine, University of Texas MD Anderson Cancer Center, Houston, TX.

Adam Sharp (A)

The Institute of Cancer Research and The Royal Marsden Hospital, London, United Kingdom.

Johann de Bono (J)

The Institute of Cancer Research and The Royal Marsden Hospital, London, United Kingdom.

Ana Aparicio (A)

Department of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX.

Mark T Fleming (MT)

US Oncology Research, Virginia Oncology Associates, Norfolk, VA.

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Classifications MeSH