[Aggressive variant prostate cancer and transdifferentiated neuroendocrine prostate cancer: from diagnosis to therapy]
- Gunhild von Amsberg 1,2, Sergey Dyshlovoy 3, Moritz Kaune 3
- Gunhild von Amsberg 1,2, Sergey Dyshlovoy 3, Moritz Kaune 3
- 1Klinik für Onkologie und Hämatologie, Onkologisches Zentrum, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Deutschland. g.von-amsberg@uke.de.
- 2Uroonkologie an der Martini-Klinik, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Deutschland. g.von-amsberg@uke.de.
- 3Klinik für Onkologie und Hämatologie, Onkologisches Zentrum, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Deutschland.
- 0Klinik für Onkologie und Hämatologie, Onkologisches Zentrum, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Deutschland. g.von-amsberg@uke.de.
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View abstract on PubMed
Summary
This summary is machine-generated.Aggressive variants of prostate cancer (AVPC) are a diverse group of tumors with unique characteristics. Research into their subtypes and new treatments, including chemotherapy and immunotherapy, is crucial for improving patient outcomes.
Area Of Science
- Oncology
- Cancer Biology
- Genetics
Context
- Aggressive variants of prostate cancer (AVPC) present unique clinical challenges, including PSA-negative progression and distinct metastatic patterns.
- AVPC are a heterogeneous group, classified into four subgroups: neuroendocrine prostate cancer (NEPC), amphicrine, androgen receptor-low, and double-negative prostate cancer.
- The transformation to AVPC involves critical tumor suppressor gene inactivation (RB1, PTEN, TP53) and epigenetic alterations driving stem cell-like properties.
Purpose
- To provide an overview of the heterogeneity and key molecular drivers of aggressive variants of prostate cancer (AVPC).
- To outline current treatment strategies and emerging therapeutic approaches for AVPC.
- To emphasize the need for clinical trial participation to advance evidence-based treatment for AVPC.
Summary
- AVPC are characterized by androgen-independent growth, PSA-negative progression, and specific metastatic patterns.
- Subtyping AVPC (NEPC, amphicrine, AR-low, double-negative) is challenging but crucial for treatment selection.
- Key molecular events include inactivation of RB1, PTEN, and TP53, alongside epigenetic changes promoting stemness.
Impact
- Understanding AVPC heterogeneity aids in developing targeted therapies.
- Current treatments involve platinum-based chemotherapy, with novel approaches including PARP inhibitors, checkpoint inhibitors, and immunomodulators.
- Promising results with T-cell engagers, especially in NEPC, highlight the potential of immunotherapy.
- Clinical trial enrollment is vital to generate robust evidence and improve treatment paradigms for aggressive prostate cancer.
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