Evaluation of Novel Treatments for Metastatic Castration-Resistant Prostate Cancer

dc.contributor.author Arslan, Cagatay
dc.contributor.author Guner, Gurkan
dc.date.accessioned 2026-04-25T10:18:33Z
dc.date.available 2026-04-25T10:18:33Z
dc.date.issued 2026-03-04
dc.description.abstract IntroductionMetastatic castration-resistant prostate cancer (mCRPC) remains a lethal disease with a median overall survival of approximately 2 years. Although major therapeutic advances have been achieved over the past two decades, many effective treatments have shifted to earlier disease settings, and significant unmet needs persist in the mCRPC population.Areas coveredThis narrative review is based on a structured literature search of PubMed/MEDLINE and Embase covering publications from January 2020 to October 2025, supplemented by ClinicalTrials.gov and major oncology congress abstracts (ASCO and ESMO). The molecular landscape of mCRPC, currently approved therapies, and emerging treatment strategies are discussed, including next-generation androgen receptor-targeted agents, PTEN/PI3K/AKT/mTOR pathway inhibitors, PSMA-targeted radioligand therapies, antibody-drug conjugates, CDK4/6 inhibitors, epigenetic modifiers, and novel immunotherapeutic approaches.Expert opinionThe therapeutic landscape of mCRPC has expanded substantially; however, treatment resistance and the absence of validated sequencing strategies continue to pose major challenges. Advancements in this field will rely on improved molecular profiling, biologically rational combination strategies, and the incorporation of predictive biomarkers to enable personalized treatment decisions. Concurrently, earlier integration of targeted therapies, radioligand approaches, and biomarker-enriched clinical trial designs is likely to reshape treatment paradigms and enhance long-term clinical outcomes.
dc.description.sponsorship Astellas Scientific and Medical Affairs; Ferring Research Institute, FRI; Bristol-Myers Squibb, BMS
dc.description.sponsorship A reviewer on this manuscript has disclosed they have received research funding from Astellas Scientific and Medical Affairs (2014–2015), Ferring Research Institute (2019), and Bristol-Myers Squibb (2020–2025). Peer reviewers on this manuscript have no other relevant financial relationships or otherwise to disclose.
dc.identifier.doi 10.1080/14656566.2026.2652456
dc.identifier.issn 1465-6566
dc.identifier.issn 1744-7666
dc.identifier.scopus 2-s2.0-105034760845
dc.identifier.uri https://hdl.handle.net/20.500.14365/9006
dc.identifier.uri https://doi.org/10.1080/14656566.2026.2652456
dc.language.iso en
dc.publisher Taylor & Francis Ltd
dc.relation.ispartof Expert Opinion on Pharmacotherapy
dc.rights info:eu-repo/semantics/closedAccess
dc.subject Metastatic Castration-Resistant Prostate Cancer
dc.subject Molecular Pathways Targeted
dc.subject Novel Approaches
dc.subject Precision Oncology
dc.subject Emerging Systemic Treatments
dc.title Evaluation of Novel Treatments for Metastatic Castration-Resistant Prostate Cancer
dc.type Article
dspace.entity.type Publication
gdc.author.scopusid 57200544019
gdc.author.scopusid 57191447331
gdc.author.wosid GUNER, GURKAN/I-9062-2013
gdc.description.department
gdc.description.departmenttemp [Guner, Gurkan; Arslan, Cagatay] Izmir Univ Econ, Med Point Hosp, Dept Med Oncol, TR-35575 Izmir, Turkiye
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
gdc.description.woscitationindex Science Citation Index Expanded
gdc.identifier.pmid 41889024
gdc.identifier.wos WOS:001731594300001
gdc.index.type PubMed
gdc.index.type WoS
gdc.index.type Scopus
gdc.virtual.author Güner, Gürkan
gdc.virtual.author Arslan, Çağatay
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