某三级医院菲律宾患者鼻咽癌中WT1的免疫组织化学表达

Criston Van Manasan, J. M. Atun, J. Carnate
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摘要

背景。鼻咽癌(NPC)是东南亚和菲律宾的地方病。由于高疾病负担和现有方式的不良影响,新的治疗方法是可取的。免疫组化检测WT1表达已在许多肿瘤中报道。此外,通过WT1肽疫苗接种的免疫治疗在多种恶性肿瘤中显示出有希望的结果。在NPC中WT1表达的研究尚未在任何人群中发表。目标。通过免疫组织化学记录鼻咽癌中WT1的表达可能为使用WT1疫苗治疗这种疾病的可能性提供见解。方法。这是一项回顾性描述性研究。选取菲律宾总医院化验室保存的2016 - 2017年所有新诊断的NPC病例标本。病例是根据具体标准纳入的。回顾每例病例的肿瘤分类,并进行WT1免疫组化染色。评估WT1免疫染色的强度。结果采用卡方检验进行相关性分析,fisher精确校正。结果。共纳入57例,均为非角化性鳞状细胞癌(NK-SCCs)。未分化型49例,分化型8例。平均年龄48岁。三分之二是男性,三分之一是女性。57例患者中17例(29.8%)WT1免疫染色阳性,均为未分化型。大多数阳性病例(82.32%)表现为细胞质表达。WT1染色与肿瘤分型有显著相关性。结论。与在其他癌症中进行的研究类似,相当一部分npc表达WT1。这一发现为探索开辟了其他途径,包括将WT1肽疫苗接种作为一种治疗选择的可行性。建议进一步研究WT1与NPC之间的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunohistochemical Expression of WT1 in Nasopharyngeal Carcinoma Among Filipino Patients in a Tertiary Hospital
Background. Nasopharyngeal carcinoma (NPC) is endemic in Southeast Asia and the Philippines. Novel treatments are desirable due to the high disease burden and adverse effects of existing modalities. Detection of WT1 expression via immunohistochemistry has been reported in many tumors. Moreover, immunotherapy via WT1 peptide vaccination has shown promising results in a wide range of malignancies. No studies on WT1 expression in NPC have been published in any population. Objective. Documenting WT1 expression in NPC via immunohistochemistry may provide insight into the possibility of using WT1 vaccination for this disease. Methodology. This was a retrospective descriptive study. All newly-diagnosed cases of NPC from 2016 to 2017 with samples stored in the Department of Laboratories of the Philippine General Hospital were considered. Cases were included based on specific criteria. The tumor classification of each case was reviewed and WT1 immunohistochemistry staining was performed. Assessment of the strength of WT1 immunostaining was conducted. The results were analyzed using Chi-square test for association with fisher exact correction. Results. A total of 57 cases were included, all of which were non-keratinizing squamous cell carcinomas (NK-SCCs). Forty-nine were undifferentiated type while eight were differentiated type. The mean age was 48 years. Two thirds were male, one third were female. Seventeen of the 57 cases (29.8%) were positive for WT1 immunostaining, and all were undifferentiated type. The majority (82.32%) of the positive cases showed cytoplasmic expression. There was a significant association between tumor classification and WT1 staining. Conclusion. Similar to studies conducted in other carcinomas, a considerable subset of NPCs express WT1. This finding opens other avenues for exploration, including the feasibility of WT1 peptide vaccination as a treatment option. Further studies on the associations between WT1 and NPC are recommended.
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