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肺腺鳞癌:生存情况、影像学表现、程序性死亡受体配体1(PD-L1)及驱动基因突变

Adenosquamous Carcinoma of the Lung: Survival, Radiologic Findings, PD-L1, and Driver Mutations.

作者信息

Illini Oliver, Fabikan Hannah, Fischer Eva, Lang-Stöberl Anna Sophie, Krenbek Dagmar, Jarius Christa, Azarnia-Medan Shokoufa, Gasser Stefan, Hochmair Maximilian Johannes, Weinlinger Christoph, Valipour Arschang, Watzka Stefan

机构信息

Department of Respiratory and Critical Care Medicine, Clinic Floridsdorf, Vienna Healthcare Group, Bruenner Straße 68, 1210 Vienna, Austria.

Karl Landsteiner Institute of Lung Research and Pulmonary Oncology, Clinic Floridsdorf, Bruenner Straße 68, 1210 Vienna, Austria.

出版信息

J Clin Med. 2024 Sep 25;13(19):5711. doi: 10.3390/jcm13195711.

Abstract

Adenosquamous carcinoma of the lung (ASC) is a rare non-small-cell lung cancer (NSCLC) subtype combining components of squamous cell carcinoma (SCC) and adenocarcinoma (AC). Data on ASC, particularly in Caucasian populations, are limited. We reviewed clinicopathological and radiological characteristics of ASC patients diagnosed between 1996 and 2023. Patients were classified into AC-predominant ASC (AC-ASC) and SCC-predominant ASC (SCC-ASC) groups for analysis. Among the 66 patients included, the median overall survival was 41.7 (95% CI, 25.0-54.4), while it was 48.1 (95% CI, 27.3-88.0) in patients treated with curative surgery (n = 44) and 15.3 (95% CI, 6.5-42.6) months for palliative patients (n = 22). The five-year survival rates were 39% and 26%, respectively. Recurrence occurred in 43% of stage I patients and was associated with worse survival (HR 3.303 (95% CI, 1.10-9.89) = 0.033). AC-ASCs (n = 17) more frequently showed air-bronchogram ( = 0.002) and pleural effusions ( = 0.054) compared to SCC-ASCs (n = 26). SCC-ASCs exhibited more vascular invasion ( = 0.006) and PD-L1 values between 1 and 49% (TPS) ( = 0.032). The subtype did not influence survival. EGFR and ALK alterations were found in 17% and 2% of patients, respectively. Despite early-stage disease, ASC patients had a high recurrence rate, associated with worse survival. Clinicopathologic differences between AC-ASCs and SCC-ASCs did not influence survival.

摘要

肺腺鳞癌(ASC)是一种罕见的非小细胞肺癌(NSCLC)亚型,由鳞状细胞癌(SCC)和腺癌(AC)成分组成。关于ASC的数据,尤其是白种人群的数据有限。我们回顾了1996年至2023年间确诊的ASC患者的临床病理和放射学特征。患者被分为以AC为主的ASC(AC-ASC)组和以SCC为主的ASC(SCC-ASC)组进行分析。在纳入的66例患者中,中位总生存期为41.7个月(95%CI,25.0 - 54.4),而接受根治性手术的患者(n = 44)为48.1个月(95%CI,27.3 - 88.0),姑息治疗患者(n = 22)为15.3个月(95%CI,6.5 - 42.6)。五年生存率分别为39%和26%。43%的I期患者出现复发,且复发与较差的生存率相关(HR 3.303(95%CI,1.10 - 9.89) = 0.033)。与SCC-ASC(n = 26)相比,AC-ASC(n = 17)更常出现空气支气管征( = 0.002)和胸腔积液( = 0.054)。SCC-ASC表现出更多的血管侵犯( = 0.006)和PD-L1值在1%至49%之间(TPS)( = 0.032)。亚型不影响生存率。分别在17%和2%的患者中发现EGFR和ALK改变。尽管处于疾病早期,ASC患者复发率高,与较差的生存率相关。AC-ASC和SCC-ASC之间的临床病理差异不影响生存率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d450/11476650/2b135a0f5d65/jcm-13-05711-g001.jpg

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