Clinical Characteristics, Treatment and Prognosis of Primary Tracheal Adenoid Cystic Carcinoma: A Multicenter Retrospective Study

IF 3.1 2区 医学 Q2 ONCOLOGY Cancer Medicine Pub Date : 2025-04-18 DOI:10.1002/cam4.70877
Yi Luo, Jun Teng, Zhina Wang, Qinyan Hong, Hang Zou, Lei Li, Nan Zhang, Hongwu Wang
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Abstract

Background

Tracheal adenoid cystic carcinoma (TACC) is a rare salivary gland malignant tumor. Previous studies mainly focused on surgery, radiation, and chemotherapy. The purpose of this study is to describe more clinical characteristics, treatments, and overall survival (OS) of TACC.

Methods

Retrospectively analyzed TACC patients from two medical institutions and the SEER database from January 2010 to December 2021. Survival curves were drawn using the Kaplan–Meier method, and the effects of prognosis were analyzed by multivariate COX regression and AFT. The endpoint of the study was overall survival (OS).

Results

One hundred fifty TACC patients were enrolled (DZM 11, EG 64, SEER 75), and the 5- and 10-year survival rate was 70.62% and 35.80%, with a median survival time of 98 months. Lymph node status (yes) is an independent risk factor for TACC (HR = 3.020, 95% CI = 1.419–6.426, p = 0.004), and surgery is an independent protective factor (HR = 0.293, 95% CI = 0.146–0.587, p = 0.001). The AFT yielded similar results. In subgroup analysis of 63 non-surgical patients, lymph node status (Yes) (HR = 3.511, 95% CI = 1.498–8.229, p = 0.004), and tumor longitudinal diameter range (TLDR) > 1 (HR = 2.975, 95% CI = 1.360–6.506, p = 0.006) are independent risk factors, while Targeted Therapy (HR = 0.248, 95% CI = 0.096–0.637, p = 0.004) is an independent protective factor.

Conclusion

Lymph node status and TLDR are prognostic factors of TACC. Surgery is associated with prolonged survival of TACC. Targeted therapy may be associated with improved survival among non-surgical TACC patients.

Trial Registration: ChiCTR2400083551

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原发性气管腺样囊性癌的临床特点、治疗及预后:一项多中心回顾性研究
背景气管腺样囊性癌是一种罕见的涎腺恶性肿瘤。以往的研究主要集中在手术、放疗和化疗方面。本研究的目的是描述更多的TACC的临床特征、治疗方法和总生存期(OS)。方法回顾性分析2010年1月至2021年12月来自两家医疗机构和SEER数据库的TACC患者。采用Kaplan-Meier法绘制生存曲线,采用多因素COX回归和AFT分析对预后的影响,研究终点为总生存期(OS)。结果纳入150例TACC患者(DZM 11例,EG 64例,SEER 75例),5年和10年生存率分别为70.62%和35.80%,中位生存时间为98个月。淋巴结状态(是)是TACC的独立危险因素(HR = 3.020, 95% CI = 1.419-6.426, p = 0.004),手术是TACC的独立保护因素(HR = 0.293, 95% CI = 0.146-0.587, p = 0.001)。AFT也得出了类似的结果。在63例非手术患者的亚组分析中,淋巴结状态(Yes) (HR = 3.511, 95% CI = 1.498 ~ 8.229, p = 0.004)和肿瘤纵径范围(TLDR) > 1 (HR = 2.975, 95% CI = 1.360 ~ 6.506, p = 0.006)是独立的危险因素,而靶向治疗(Targeted Therapy) (HR = 0.248, 95% CI = 0.096 ~ 0.637, p = 0.004)是独立的保护因素。结论淋巴结状态和TLDR是TACC的预后因素。手术可延长TACC患者的生存期。靶向治疗可能与非手术治疗的TACC患者的生存率提高有关。试验注册:ChiCTR2400083551
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来源期刊
Cancer Medicine
Cancer Medicine ONCOLOGY-
CiteScore
5.50
自引率
2.50%
发文量
907
审稿时长
19 weeks
期刊介绍: Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas: Clinical Cancer Research Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations Cancer Biology: Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery. Cancer Prevention: Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach. Bioinformatics: Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers. Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.
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