PO.ET06.05 · 实验与分子治疗
高TROP2表达在头颈癌中常见并与淋巴结转移相关
High TROP2 expression is frequent and linked to nodal metastasis in head and neck cancer
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
头颈癌构成一组高度异质性的恶性肿瘤,临床结局各不相同。尽管在手术、放疗和全身治疗方面取得了进展,全球每年仍有超过30万患者死于这些癌症。因此,迫切需要鉴定新的分子标志物,以改善患者分层并指导个体化治疗策略。膜糖蛋白滋养层细胞表面抗原2(TROP2)是sacituzumab govitecan(SG)的分子靶点,SG是一种抗体-药物偶联物,已获批用于治疗转移性三阴性乳腺癌和晚期尿路上皮癌。此外,它在其他肿瘤类型(如非小细胞肺癌和胃肠道癌)中也显示出有前景的临床活性。为评估TROP2表达在头颈癌中的患病率和潜在临床意义,我们采用免疫组化(IHC)以组织微阵列形式分析了共583例头颈癌。采用H评分分析将癌症定义为强阳性(h评分300)、中度阳性(200-299)、弱阳性(1-199)或阴性(0)。在531例可评估的头颈癌中,TROP2表达强阳性占53.7%,中度阳性占18.8%,弱阳性占22.8%,阴性占4.7%。不同部位肿瘤之间的TROP2表达存在显著差异。TROP2强表达见于336例口咽癌中的61.2%、25例下咽癌中的48.0%、143例喉癌中的40.1%、8例口腔癌中的37.5%,以及14例鼻咽癌中的21.4%(p=0.0028)。在347例有pN分期数据的患者中,高TROP2表达与淋巴结转移相关(p=0.0002)。然而,TROP2表达水平在统计学上与pT分期(p=0.3206)、恶性程度的组织学分级(p=0.7732)、远处转移的存在(M1,p=0.4024)、L状态(p=0.2895)和V状态(p=0.6822)无关。根据我们的数据得出结论,高水平TROP2表达在头颈癌中非常常见。因此,许多患有这些肿瘤的患者可能从SG治疗中获益。TROP2表达水平的部位特异性差异很可能由头颈癌各亚型的部位特异性危险因素所驱动。
查看英文原文 English abstract
Head and neck cancers constitute a highly heterogeneous group of malignancies exhibiting variable clinical outcomes. Despite advances in surgery, radiotherapy, and systemic treatments, more than 300,000 patients worldwide die annually from these cancers. The identification of novel molecular markers to improve patient stratification and to guide personalized treatment approaches is therefore urgently needed. The membrane glycoprotein Trophoblast cell surface antigen 2 (TROP2) is the molecular target of sacituzumab govitecan (SG), an antibody-drug conjugate that has been approved for the treatment of metastatic triple-negative breast cancer and advanced urothelial carcinomas. Additionally, it has shown promising clinical activity in other tumor types, such as non-small cell lung cancer, and gastrointestinal cancers. To evaluate the prevalence and potential clinical significance of TROP2 expression in head and neck cancer, we analyzed a total of 583 head and neck cancers by immunohistochemistry (IHC) in a tissue microarray format. H score analysis was used to define cancers as strongly positive (h-score 300), moderately positive (200-299), weakly positive (1-199), or negative (0). TROP2 expression was found to be strong in 53.7%, moderate in 18.8%, weak in 22.8%, and negative in 4.7% of 531 evaluable head and neck carcinomas. There was a marked variability of TROP2 expression between tumors of different localization. TROP2 expression was found to be strong in 61.2% of 336 carcinomas of the oropharynx, 48.0% of 25 cancers of the hypopharynx, 40.1% of 143 cancers of the larynx, 37.5% of 8 carcinomas of the oral cavity, and in 21.4% of 14 carcinomas of the nasopharynx (p=0.0028). Among 347 patients with data on the pN-stage, high TROP2 expression was associated with nodal metastasis (p=0.0002). However, the level of TROP2 expression was statistically unrelated to pT-stage (p=0.3206), histologic grade of malignancy (p=0.7732), presence of distant metastasis (M1, p=0.4024), L-status (p=0.2895), and V-status (p=0.6822). It is concluded from our data, that high level TROP2 expression is very common in head and neck cancers. Accordingly, many patients with these tumors could potentially benefit from SG treatment. Site specific differences in TROP2 expression levels are likely to be driven by location-specific risk factors for subtypes of head and neck cancers.
利益披露 Disclosure
D. Dum, None..
J. Knief, None..
C. Thorns, None..
M. Freytag, None..
F. Lutz, None..
W. Wilczak, None..
K. Möller, None..
F. Viehweger, None..
F. Gehrisch, None..
N. Schraps, None..
C. Hube-Magg, None..
M. Kluth, None..
M. C. Tsourlakis, None..
R. Simon, None.
G. Sauter,
MS Validated Antibodies, Hamburg, Germany Other, TROP2 antibody clone MSVA-733R was provided from MS Validated Antibodies GmbH (owned by a family member of GS)..
N. Gorbokon, None..
M. Hamad, None..
N. Möckelmann, None..
T. Clauditz, None..
A. Münscher, None..
V. Chirico, None.