局部晚期黑色素瘤患者分离肢体灌注治疗前肿瘤微环境与治疗结果的关系

IF 2.6 3区 医学 Q2 CELL BIOLOGY
Sanni K. A. Tulokas, Susanna Juteau, Siru P. Mäkelä, Katja E. Välimäki, Teijo Pellinen, Micaela M. Hernberg
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引用次数: 0

摘要

随着有效的黑色素瘤治疗方法的出现,利用孤立肢体灌注(ILP)治疗局限于肢体的不可切除黑色素瘤的方法已经减少。然而,一些患者仍然从ILP中获得长期益处。我们旨在确定预处理肿瘤微环境(TME)的特征,以确定可能受益于ILP的患者。对2008年至2018年在赫尔辛基大学医院接受ILP治疗的22例患者的前转移性黑色素瘤样本进行多重免疫组织化学(mIHC)和数字图像分析。抗体组评估免疫细胞在瘤内和瘤外的比例。我们检查了ILP后的治疗反应和中位无进展生存期(PFS)是否与TME的结果相关。PFS与肿瘤内腔室(CD3+、CD4+和CD11c+细胞)较低的免疫细胞浸润量呈正相关,瘤外腔室免疫细胞数量增加与PFS较长相关(CD3+、CD4+、CD8+,均表达PD-1)。此外,一些免疫细胞亚群的分布与完全治疗反应相关(PD-1/ pd - l1阳性CD4+和PD-1阳性CD8+细胞)。我们的研究结果表明,如果转移灶表现出肿瘤内特异性免疫细胞亚型的较低分布和肿瘤外某些免疫细胞亚型的较高分布,则患者可能具有更好的ILP预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association of Pretreatment Tumour Microenvironment and Treatment Outcome in Patients With Locally Advanced Melanoma Treated With Isolated Limb Perfusion

Association of Pretreatment Tumour Microenvironment and Treatment Outcome in Patients With Locally Advanced Melanoma Treated With Isolated Limb Perfusion

As effective melanoma treatments have become available, utilizing isolated limb perfusion (ILP) to treat unresectable melanoma limited to the limb has decreased. However, some patients still receive long-term benefits from ILP. We aimed to identify features of the pretreatment tumor microenvironment (TME) to identify patients who may benefit from ILP. Pretreatment metastatic melanoma samples from 22 patients treated at Helsinki University Hospital with ILP from 2008 to 2018 were analyzed with multiplex immunohistochemistry (mIHC) and digital image analysis. Antibody panels evaluated the proportions of immune cells in the intratumoral and extratumoral compartments. We examined whether treatment response and median progression-free survival (PFS) after ILP correlated to findings in the TME. A statistically significant positive correlation was found between PFS and lower immune cell infiltrations in the intratumoral compartment (CD3+, CD4+, and CD11c+ cells), and increased numbers of immune cells in the extratumoral compartment were associated with longer PFS (CD3+, CD4+, CD8+, all expressing PD-1). Furthermore, the distribution of some immune cell subsets correlated with complete treatment response (PD-1/PD-L1-positive CD4+ and PD-1-positive CD8+ cells). Our results suggest that patients may have a better ILP outcome if the metastases exhibit a lower distribution of specific immune cell subtypes intratumorally and a higher extratumoral distribution of some immune cell subtypes.

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来源期刊
Pigment Cell & Melanoma Research
Pigment Cell & Melanoma Research 医学-皮肤病学
CiteScore
8.90
自引率
2.30%
发文量
54
审稿时长
6-12 weeks
期刊介绍: Pigment Cell & Melanoma Researchpublishes manuscripts on all aspects of pigment cells including development, cell and molecular biology, genetics, diseases of pigment cells including melanoma. Papers that provide insights into the causes and progression of melanoma including the process of metastasis and invasion, proliferation, senescence, apoptosis or gene regulation are especially welcome, as are papers that use the melanocyte system to answer questions of general biological relevance. Papers that are purely descriptive or make only minor advances to our knowledge of pigment cells or melanoma in particular are not suitable for this journal. Keywords Pigment Cell & Melanoma Research, cell biology, melatonin, biochemistry, chemistry, comparative biology, dermatology, developmental biology, genetics, hormones, intracellular signalling, melanoma, molecular biology, ocular and extracutaneous melanin, pharmacology, photobiology, physics, pigmentary disorders
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