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[头颈部鳞状细胞癌年轻患者的诱变敏感性与二次癌症风险]

[Mutagen sensitivity and risk of second cancer in young patients with head and neck squamous cell cancer].

作者信息

Bukovszky Botond, Fodor János, Székely Gábor, Kocsis Zsuzsa S, Oberna Ferenc, Major Tibor, Takácsi-Nagy Zoltán, Polgár Csaba, Jurányi Zsolt

机构信息

Sugárterápiás Központ, Országos Onkológiai Intézet, Budapest, Hungary.

Fej-nyaki Daganatok Multidiszciplináris Központ, Országos Onkológiai Intézet, Budapest, Hungary.

出版信息

Magy Onkol. 2021 Mar 17;65(1):39-45. Epub 2019 Jul 10.

Abstract

Head and neck cancer patients are at high risk for secondary primary cancer (SPC) development. Mutagen hypersensitivity may be associated with elevated risk of SPC. A survey was made of SPC among 124 young (≤50 years) patients with squamous cell carcinoma of the head and neck who were enrolled in a pretreatment mutagen sensitivity investigation during 1996-2006. Mutagen sensitivity was assessed by exposing lymphocytes to bleomycin in vitro and quantitating the bleomycin-induced chromatid breaks per cell (b/c). Patients were classified as hypersensitive (>1 b/c) or not hypersensitive (≤1 b/c). The mean follow-up time was 64 months (range: 5-244 months). Eighteen patients (15%) developed a SPC. The 10-year estimated rate of SPC for hypersensitive (n=65) or not hypersensitive (n=59) patients were 17% and 30%, respectively (p=0.4272). Thirty-nine percent of SPC was developed after 10-year follow-up. The 5-year cancer-specific survival was 17% following the development of SPC. According to our findings, mutagen hypersensitivity does not increase the risk of developing SPC.

摘要

头颈癌患者发生第二原发性癌症(SPC)的风险很高。诱变超敏反应可能与SPC风险升高有关。对1996年至2006年期间参与预处理诱变敏感性调查的124例年轻(≤50岁)头颈鳞状细胞癌患者的SPC情况进行了一项调查。通过在体外将淋巴细胞暴露于博来霉素并定量每个细胞中博来霉素诱导的染色单体断裂数(b/c)来评估诱变敏感性。患者被分类为超敏(>1 b/c)或非超敏(≤1 b/c)。平均随访时间为64个月(范围:5 - 244个月)。18例患者(15%)发生了SPC。超敏(n = 65)或非超敏(n = 59)患者的SPC 10年估计发生率分别为17%和30%(p = 0.4272)。39%的SPC是在10年随访后发生的。SPC发生后的5年癌症特异性生存率为17%。根据我们的研究结果,诱变超敏反应不会增加发生SPC的风险。

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