Interventional Pulmonology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy.
Pathology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy.
Respiration. 2021;100(6):515-522. doi: 10.1159/000514316. Epub 2021 Apr 7.
Diagnosis, staging, and molecular profiling of lung cancer are mostly carried out with bronchoscopy or CT-guided aspiration/biopsy. However, patients with locally advanced or advanced disease often harbor "superficial" metastases for which a percutaneous, ultrasound-assisted needle aspiration/biopsy (US-NAB) might represent an equally effective yet less invasive and costly alternative.
We reviewed a prospectively collected database of consecutive patients with known/suspected lung cancer who underwent a US-NAB of a suspected "superficial" metastasis. Cancer genotyping was carried out with next-generation sequencing using the Oncomine™ Focus DNA and RNA fusion panels. PD-L1 immunohistochemistry was performed with the SP263 antibody. Feasibility, diagnostic yield for tissue diagnosis, sensitivity for malignancy, diagnostic yield for the molecular profiling, and complications were the study endpoints.
A total of 98 lesions were evaluated, and 93 were biopsied (95% feasibility). The spectrum of sampled sites included lymph nodes (63 patients), bone (11), subcutaneous tissue (8), muscle (7), and the pleura (4). The diagnostic yield for a tissue diagnosis was 93% (91/98). US-NAB correctly identified 85 of the 87 patients finally diagnosed with malignancy (98% sensitivity). Cancer genotyping and PDL1 testing were successfully completed in 41/42 patients (98%) and in 40/50 patients (80%) for whom these tests were requested, respectively. No complications were observed.
US-NAB of "superficial" metastasis of lung cancer is safe and is associated with high success for diagnosis and molecular profiling. In this clinical setting, using US-NAB as a first-step technique would significantly limit the use of more invasive and costly diagnostic procedures.
肺癌的诊断、分期和分子分析主要通过支气管镜或 CT 引导下的抽吸/活检进行。然而,局部晚期或晚期疾病的患者常存在“表浅”转移,经皮超声辅助下的针吸/活检(US-NAB)可能是一种同样有效的、侵袭性更小、花费更低的替代方法。
我们回顾了一项连续收集的数据库,包括已知/疑似患有肺癌并接受疑似“表浅”转移灶 US-NAB 的患者。使用 Oncomine™ Focus DNA 和 RNA 融合面板进行下一代测序以进行癌症基因分型。使用 SP263 抗体进行 PD-L1 免疫组化染色。本研究的终点为可行性、组织诊断的诊断率、恶性肿瘤的敏感性、分子分析的诊断率和并发症。
共评估了 98 个病灶,93 个病灶进行了活检(95%的可行性)。采样部位的范围包括淋巴结(63 例)、骨(11 例)、皮下组织(8 例)、肌肉(7 例)和胸膜(4 例)。组织诊断的诊断率为 93%(91/98)。US-NAB 正确识别了 87 例最终诊断为恶性肿瘤的患者中的 85 例(98%的敏感性)。41/42 例(98%)和 40/50 例(80%)患者成功完成了癌症基因分型和 PD-L1 检测,这些检测分别是为这 41/42 例和 40/50 例患者要求的。未观察到并发症。
US-NAB 对肺癌“表浅”转移是安全的,且与高诊断和分子分析成功率相关。在这种临床情况下,将 US-NAB 作为第一步技术可以显著限制更具侵袭性和花费更高的诊断程序的使用。