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原发灶不明的恶性黑色素瘤。长话短说。对文献的系统回顾。

Malignant melanoma of unknown primary site. To make the long story short. A systematic review of the literature.

机构信息

Panhellenic Association for Continual Medical Research (PACMeR), Greece.

出版信息

Crit Rev Oncol Hematol. 2011 May;78(2):112-26. doi: 10.1016/j.critrevonc.2010.04.007. Epub 2010 May 31.

Abstract

INTRODUCTION

Although more than 90% of melanomas have a cutaneous origin, occasionally it is discovered as a secondary deposit without evident primary site. The aim of this study was to systematically review published literature and analyse data on incidence, presentation, therapeutic interventions, survival and prognostic factors.

METHODS

We searched MEDLINE, (search terms Melanom*, unknown origin, unknown primary, indolent, occult) and the abstracts from major congresses of the last 4 years and perused the references of the retrieved relevant articles.

RESULTS

4348 patients with MUP were reported along with 132,643 patients with Melanoma of Known Primary (MKP). The incidence of MUP was 3.2%. The male to female ratio was 2:1 while the age peak was in the 4th and 5th decades. MUP patients harbouring nodal disease had a median overall survival ranging between 24 and 127 months, 5-year survival rate between 28.6% and 75.6% and 10-year survival rate between 18.8% and 62.9%. MUP patients with visceral disease had median survival times between 3 and 16 months, and 5-year survival rates between 5.9% and 18%. Presence of tumour regression in metastatic sites and low nodal burden were associated with favourable outcome. Potentially curative surgical treatment offered survival advantage in comparison to patients with residual metastatic foci. MUP patients who received adjuvant chemotherapy or radiotherapy paradoxically seemed to fare worse compared to patients observed.

CONCLUSIONS

This is the first review to bring together the information of 89 years and to analyze all the potential information accumulated. Although a well know entity no consensus is reached in order to describe MUP presentation, management or prognosis.

摘要

简介

尽管超过 90%的黑色素瘤起源于皮肤,但偶尔也会发现没有明显原发性肿瘤的继发性转移。本研究旨在系统地回顾已发表的文献,并分析发病率、表现、治疗干预、生存和预后因素的数据。

方法

我们检索了 MEDLINE(检索词为 Melanom*、未知起源、未知原发性、惰性、隐匿性)和过去 4 年主要会议的摘要,并查阅了相关文章的参考文献。

结果

报告了 4348 例 MUP 患者和 132643 例已知原发性黑色素瘤(MKP)患者。MUP 的发病率为 3.2%。男女比例为 2:1,年龄高峰在第 4 和第 5 个十年。存在淋巴结疾病的 MUP 患者的总生存中位数范围为 24 至 127 个月,5 年生存率为 28.6%至 75.6%,10 年生存率为 18.8%至 62.9%。存在内脏疾病的 MUP 患者的中位生存时间为 3 至 16 个月,5 年生存率为 5.9%至 18%。转移部位肿瘤消退和低淋巴结负荷与良好的预后相关。与残留转移灶患者相比,接受潜在治愈性手术治疗的患者具有生存优势。接受辅助化疗或放疗的 MUP 患者的预后似乎比观察患者更差,这令人费解。

结论

这是首次综述汇集了 89 年来的信息,并分析了所有积累的潜在信息。尽管是一个众所周知的实体,但尚未就 MUP 的表现、管理或预后达成共识。

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