Department of Otorhinolaryngology, Head and Neck Surgery, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Department of Pathology and Medical Biology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Am J Otolaryngol. 2024 Sep-Oct;45(5):104424. doi: 10.1016/j.amjoto.2024.104424. Epub 2024 Jul 22.
Diagnostic endoscopy with biopsy under general anesthesia (DE-GA) is still considered as the established standard to assess laryngopharyngeal cancer patients. Office-based flexible laryngoscopic biopsy (FLB) offers an alternative, but the effect on oncological outcome remains uncertain. Therefore, the diagnostic process and survival of patients undergoing FLB, compared to those undergoing DE-GA were evaluated.
Patients suspected of laryngopharyngeal cancer who underwent FLB were evaluated. Patients with FLB-confirmed squamous cell carcinoma (SCC) were matched with DE-GA patients based on tumor site, T-classification, N-classification, age, and p16 overexpression. Time from first visit to diagnosis (FVD), time to treatment interval (TTI), disease-specific survival (DSS) and overall survival (OS) were analyzed.
FLB yielded a definitive diagnosis in 155/164 (95 %) patients. No complications were observed. Ninety-eight of the 124 patients in which FLB revealed a SCC received curative treatment and were compared with 98 matched patients who underwent DE-GA. Median FVD interval was 6 days after FLB and 15 days after DE-GA (p < 0.001). Median TTI interval (FLB: 28 days, DE-GA: 28 days) was equal (p = 0.91). Oncological outcomes were comparable (p > 0.05) between FLB (OS: 2-yr: 76 %, 5-yr: 42 %; DSS: 2-yr: 86 %, 5-yr: 85 %) and DE-GA groups (OS: 2-yr: 76 %, 5-yr: 50 %; DSS: 2-yr: 81 %, 5-yr: 79 %).
FLB in the outpatient setting demonstrates a high diagnostic accuracy, is safe, accelerates the diagnostic process and has no negative effects on clinical outcome compared to DE-GA. Therefore, FLB should be considered as the standard diagnostic procedure in patients suspected of laryngopharyngeal cancer.
在全身麻醉下进行诊断性内镜检查和活检(DE-GA)仍然被认为是评估喉咽癌患者的既定标准。在办公室进行的软性喉镜活检(FLB)提供了一种替代方法,但对肿瘤学结果的影响仍不确定。因此,评估了接受 FLB 和 DE-GA 的患者的诊断过程和生存情况。
评估了疑似患有喉咽癌并接受 FLB 的患者。对接受 FLB 确诊为鳞状细胞癌(SCC)的患者,根据肿瘤部位、T 分类、N 分类、年龄和 p16 过表达情况,与接受 DE-GA 的患者进行匹配。从首次就诊到诊断的时间(FVD)、治疗间隔时间(TTI)、疾病特异性生存率(DSS)和总生存率(OS)进行了分析。
FLB 对 164 例患者中的 155 例(95%)做出了明确诊断。未观察到并发症。在 124 例 FLB 显示 SCC 的患者中,98 例接受了治愈性治疗,并与 98 例接受 DE-GA 的匹配患者进行了比较。FLB 后中位 FVD 间隔为 6 天,DE-GA 后为 15 天(p<0.001)。中位 TTI 间隔(FLB:28 天,DE-GA:28 天)相等(p=0.91)。FLB(OS:2 年:76%,5 年:42%;DSS:2 年:86%,5 年:85%)和 DE-GA 组之间的肿瘤学结果相当(OS:2 年:76%,5 年:50%;DSS:2 年:81%,5 年:79%)(p>0.05)。
在门诊环境下进行的 FLB 具有较高的诊断准确性,是安全的,可加速诊断过程,与 DE-GA 相比,对临床结果没有负面影响。因此,FLB 应被视为疑似喉咽癌患者的标准诊断程序。