Literature DB >> 27446387

Rapid progression of mixed neuroendocrine carcinoma-acinar adenocarcinoma of the prostate: A case report.

Jingchao Wei1, Xiaoping Zheng1, Liuxun Li1, Wensu Wei1, Zhi Long1, Leye He1.   

Abstract

The current study presents the case of a 78-year-old male with mixed neuroendocrine (NE) carcinoma-acinar adenocarcinoma of the prostate. The patient received endocrine therapy (maximal androgen blockade) after the initial diagnosis resulting in a significant decrease in serum prostate-specific antigen (PSA) level. The patient underwent transurethral resection of the prostate after 6 months of androgen-deprivation therapy for extraordinarily salient difficulty in urination, and histopathology demonstrated mixed NE carcinoma-acinar adenocarcinoma once again. The NE prostate cancer progressed rapidly even though the serum PSA was controlled at a low level on account of the endocrine therapy. Previous treatment protocols were replaced by combined chemotherapy and endocrine therapy, and the patient responded well. The patient's serum PSA remained at a low level, however, urethral dilatation for acute urinary retention was required again 5 months later and the lower urinary tract symptoms became increasingly evident. The patient eventually died of cachexia.. These findings indicate that mixed NE carcinoma-acinar adenocarcinoma has a higher degree of malignancy and that endocrine therapy for prostate cancer has a propensity to facilitate progression of this tumor.

Entities:  

Keywords:  endocrine therapy; neuroendocrine prostate cancer; rapid progression

Year:  2016        PMID: 27446387      PMCID: PMC4950814          DOI: 10.3892/ol.2016.4737

Source DB:  PubMed          Journal:  Oncol Lett        ISSN: 1792-1074            Impact factor:   2.967


  17 in total

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  1 in total

1.  Development and characterization of a cancer cachexia model employing a rare human duodenal neuroendocrine carcinoma-originating cell line.

Authors:  Kazuyoshi Yanagihara; Takanori Kubo; Yuki Iino; Keichiro Mihara; Chie Morimoto; Toshio Seyama; Takeshi Kuwata; Atsushi Ochiai; Hiroshi Yokozaki
Journal:  Oncotarget       Date:  2019-03-29
  1 in total

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