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Neuroendocrine prostate carcinoma-understanding, diagnosing, treating
被引:0
|作者:
von Amsberg, Gunhild
[1
,2
]
Dum, David
[3
]
Sauer, Markus
[4
]
Tilki, Derya
[2
]
Kaune, Moritz
[1
]
机构:
[1] Univ Klinikum Hamburg Eppendorf, Onkol Zentrum, Hamburg, Germany
[2] Univ Klinikum Hamburg Eppendorf, Martini Klin, Hamburg, Germany
[3] Univ Klinikum Hamburg Eppendorf, Inst Pathol, Hamburg, Germany
[4] Univ Klinikum Hamburg Eppendorf, Diagnost & Intervent Radiol & Nuklearmed, Hamburg, Germany
来源:
关键词:
Neuroendocrine transdifferentiation;
Androgen-independent growth;
DLL3;
protein;
human;
Platinum-based chemotherapy;
Bispecific T-cell engagers;
SMALL-CELL CARCINOMA;
PHASE-II;
CANCER;
ETOPOSIDE;
CARBOPLATIN;
CISPLATIN;
DOCETAXEL;
D O I:
10.1007/s00761-025-01681-9
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Neuroendocrine prostate carcinoma (NEPC) is an aggressive variant of prostate cancer characterized by a high proliferation rate, expression of neuroendocrine markers in tissue and serum, androgen-independent tumor growth, and a metastatic pattern that is unusual for prostate cancer. In < 1% of cases, NEPC is already present at diagnosis; most NEPC develop during the course of treatment as a result of a transdifferentiation process. This multifactorial process is determined by various genetic and epigenetic alterations. Escalating treatment to target the androgen receptor signal transduction pathway appears to play a key role. To date, there is no generally recognized treatment standard. In first-line therapy, platinum-based chemotherapy is usually used in combination with etoposide or possibly a taxane. Immunotherapeutic approaches and targeted treatment strategies are currently undergoing clinical development. Due to the still limited evidence, patients should be included in clinical trials and recorded in registries.
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页码:337 / 346
页数:10
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