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Large Cell Neuroendocrine Carcinoma of the Prostate: A Systematic Review and Pooled Analysis

机译:前列腺大细胞神经内分泌癌:系统审查和汇总分析

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摘要

Background: Large cell neuroendocrine carcinoma (LCNEC) of the prostate is an extremely rare entity, and the clinicopathological course, potential effective treatment, and prognosis are yet to be elucidated. Materials and Methods: A systematic search in Pubmed, Embase, and Ovid from inception to January 2019 was conducted. We reviewed each individual case of prostatic LCNEC and summarized specific features and outcomes for this rare pathologic entity. Results: Thirteen studies with a total of 20 patients (mean age: 70.3, range 43-87) were included in our review. Seventeen patients harbored primary LCNEC of the prostate, of which 9 patients were diagnosed with de novo carcinoma, and 8 patients were with a history of prostatic adenocarcinoma treated with hormonal therapy (mean duration: 2.9 years, range 2-5). The other 3 patients were diagnosed with metastatic LCNEC originating from lung (2 cases) and bladder (1 case). All patients met the diagnostic criteria of the typical morphological features as well as immunohistochemical staining results. Nearly all primary de novo LCNEC of the prostate were at a late stage at initial diagnosis. The pattern of distant metastasis resembled that of prostatic adenocarcinoma with the most common sites as bone spread (8/16, 50%). Most patients received systematic chemotherapy after diagnosis; however, the prognosis remained poor and patients deteriorated rapidly but with exception. Three reported cases in the context of de novo LCNEC admixed with prostatic adenocarcinoma kept sustained response to androgen deprivation therapy (ADT) and achieved obviously better survival outcomes compared with other patients. Conclusions: LCNEC of the prostate is a rare entity that mostly occurs after long-standing hormonal therapy of prostatic adenocarcinoma. The prognosis was universally poor irrespective of the systematic chemotherapy. However, patients of de novo tumor mixed with prostatic adenocarcinoma may respond to ADT and harbor a better outcome than those of pure de novo or post-ADT LCNEC of the prostate.
机译:背景:前列腺的大细胞神经内分泌癌(LCNEC)是一种极其罕见的实体,临床病理过程,潜在的有效治疗和预后尚未阐明。物料和方法:从成立于2019年1月,在PubMed,Embase和Ovid中进行了系统搜索。我们审查了每个罕见的公然实体的前列腺LCNEC的每个案例,并概述了特定的特征和结果。结果:33项研究总共20名患者(平均:70.3,范围43-87)均被审查。患有前列腺初级LCNEC的17名患者,其中9名患者被诊断为Novo癌症,8名患者患有激素治疗治疗前列腺腺癌的历史(平均持续时间:2.9岁,范围2-5)。另外3名患者被诊断出源自肺(2例)和膀胱(1例)的转移性LCNEC。所有患者均符合典型形态特征的诊断标准以及免疫组织化学染色结果。几乎所有前列腺的初级Novo LCNEC都在初步诊断时处于晚期。远处转移的模式类似于前列腺腺癌,具有最常见的位点作为骨头扩散(8/16,50%)。大多数患者在诊断后接受系统化疗;然而,预后仍然贫困,患者迅速恶化,但具有例外。在De Novo LCNEC的上下文中与前列腺腺癌混合的三个报告病例对雄激素剥夺治疗(ADT)保持持续反应,与其他患者相比,达到了明显的存活结果。结论:前列腺的LCNEC是一种罕见的实体,主要发生在前列腺腺癌的长期荷尔蒙治疗后。无论系统化疗如何,预后都普遍差。然而,与前列腺腺癌混合的Novo肿瘤患者可能会响应ADT并含有比Pure De Novo或前列腺后的纯粹液相识的结果更好。

著录项

  • 来源
    《Urologia internationalis》 |2019年第4期|共8页
  • 作者单位

    Sichuan Univ West China Hosp Inst Urol Dept Urol 37 Guoxue Lane Chengdu 610041 Sichuan;

    Sichuan Univ West China Hosp West China Sch Clin Med Chengdu Sichuan Peoples R China;

    Sichuan Univ West China Med Sch West China Hosp Dept Pathol &

    Lab Pathol State Key Lab;

    Sichuan Univ West China Hosp Inst Urol Dept Urol 37 Guoxue Lane Chengdu 610041 Sichuan;

    Sichuan Univ West China Hosp Inst Urol Dept Urol 37 Guoxue Lane Chengdu 610041 Sichuan;

    Sichuan Univ West China Hosp West China Sch Clin Med Chengdu Sichuan Peoples R China;

    Sichuan Univ West China Hosp Inst Urol Dept Urol 37 Guoxue Lane Chengdu 610041 Sichuan;

    Sichuan Univ West China Hosp Inst Urol Dept Urol 37 Guoxue Lane Chengdu 610041 Sichuan;

    Sichuan Univ West China Hosp Inst Urol Dept Urol 37 Guoxue Lane Chengdu 610041 Sichuan;

    Sichuan Univ West China Hosp Inst Urol Dept Urol 37 Guoxue Lane Chengdu 610041 Sichuan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 泌尿科学(泌尿生殖系疾病);
  • 关键词

    Prostate cancer; Large cell; Neuroendocrine carcinoma;

    机译:前列腺癌;大细胞;神经内分泌癌;

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