Immunohistological evaluation of patients treated with intra-arterial chemoradiotherapy and surgery for oral cancer.

IF 1.2 4区 医学 Q3 PATHOLOGY Medical Molecular Morphology Pub Date : 2023-12-01 Epub Date: 2023-07-29 DOI:10.1007/s00795-023-00367-8
Yutaro Ikeuchi, Masanori Someya, Tomokazu Hasegawa, Masato Saito, Shoh Mafune, Takaaki Tsuchiya, Mio Kitagawa, Toshio Gocho, Hironari Dehari, Kazuhiro Ogi, Takanori Sasaki, Yoshihiko Hirohashi, Toshihiko Torigoe, Naoki Hirokawa, Akihiro Miyazaki, Koh-Ichi Sakata
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Abstract

Preoperative intra-arterial chemoradiotherapy (IACRT) can improve the outcome and reduce the extent of surgery in patients with advanced oral cancer. However, the response to this regimen varies among patients, which may be related to the immune status of the tumor. We investigated the effects of proteins involved in tumor immunity on the outcomes of combined IACRT and surgery for oral cancer. We examined CD8 + and FoxP3 + tumor-infiltrating lymphocytes (TILs) and programmed death ligand 1 (PD-L1) expression on immune cells and tumor cells in pretreatment biopsy samples from 69 patients diagnosed with oral cancer treated with IACRT at our institution during 2000-2020. Patients with abundant CD8 + TILs had significantly better 5-year disease-specific survival (DSS) compared to that of patients with less infiltration of these cells (P = 0.016). Patients with higher FoxP3 + T-cells invasion had significantly better DSS compared to that of less FoxP3 (P = 0.005). Patients with high PD-L1 expression in tumor cells and immune cells had significantly better DSS than that of patients with low PD-L1 expression in these cells (P = 0.009 and P = 0.025, respectively). Collectively, these results suggest that the tumor immune microenvironment could affect outcomes of IACRT treatment in oral cancer.

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口腔癌动脉内放化疗及手术治疗患者的免疫组织学评价。
术前动脉内放化疗(IACRT)可以改善晚期口腔癌患者的预后,减少手术的范围。然而,患者对该方案的反应各不相同,这可能与肿瘤的免疫状态有关。我们研究了参与肿瘤免疫的蛋白对口腔癌联合IACRT和手术治疗结果的影响。我们检测了2000-2020年在我院接受IACRT治疗的69例口腔癌患者的预处理活检样本中免疫细胞和肿瘤细胞上CD8 +和FoxP3 +肿瘤浸润淋巴细胞(TILs)和程序性死亡配体1 (PD-L1)的表达。CD8 + TILs丰富的患者的5年疾病特异性生存(DSS)明显优于这些细胞浸润较少的患者(P = 0.016)。FoxP3 + t细胞侵袭高的患者DSS明显优于FoxP3侵袭低的患者(P = 0.005)。肿瘤细胞和免疫细胞中PD-L1高表达患者的DSS明显优于这些细胞中PD-L1低表达患者(P = 0.009和P = 0.025)。总之,这些结果表明肿瘤免疫微环境可能影响IACRT治疗口腔癌的结果。
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来源期刊
Medical Molecular Morphology
Medical Molecular Morphology 医学-病理学
CiteScore
2.90
自引率
5.60%
发文量
30
审稿时长
>12 weeks
期刊介绍: Medical Molecular Morphology is an international forum for researchers in both basic and clinical medicine to present and discuss new research on the structural mechanisms and the processes of health and disease at the molecular level. The structures of molecules, organelles, cells, tissues, and organs determine their normal function. Disease is thus best understood in terms of structural changes in these different levels of biological organization, especially in molecules and molecular interactions as well as the cellular localization of chemical components. Medical Molecular Morphology welcomes articles on basic or clinical research in the fields of cell biology, molecular biology, and medical, veterinary, and dental sciences using techniques for structural research such as electron microscopy, confocal laser scanning microscopy, enzyme histochemistry, immunohistochemistry, radioautography, X-ray microanalysis, and in situ hybridization. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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