New immune phenotypes for treatment response in high-grade serous ovarian carcinoma patients

C. F. Torkildsen, Marie Austdal, A. H. Jarmund, K. Kleinmanns, Eva Karin Lamark, Elisabeth Berge Nilsen, Ingunn Stefansson, R. K. Sande, Ann-Charlotte Iversen, L. Thomsen, Line Bjørge
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Abstract

Despite advances in surgical and therapeutic approaches, high-grade serous ovarian carcinoma (HGSOC) prognosis remains poor. Surgery is an indispensable component of therapeutic protocols, as removal of all visible tumor lesions (cytoreduction) profoundly improves the overall survival. Enhanced predictive tools for assessing cytoreduction are essential to optimize therapeutic precision. Patients’ immune status broadly reflects the tumor cell biological behavior and the patient responses to disease and treatment. Serum cytokine profiling is a sensitive measure of immune adaption and deviation, yet its integration into treatment paradigms is underexplored. This study is part of the IMPACT trial (NCT03378297) and aimed to characterize immune responses before and during primary treatment for HGSOC to identify biomarkers for treatment selection and prognosis. Longitudinal serum samples from 22 patients were collected from diagnosis until response evaluation. Patients underwent primary cytoreductive surgery or neoadjuvant chemotherapy (NACT) based on laparoscopy scoring. Twenty-seven serum cytokines analyzed by Bio-Plex 200, revealed two immune phenotypes at diagnosis: Immune High with marked higher serum cytokine levels than Immune Low. The immune phenotypes reflected the laparoscopy scoring and allocation to surgical treatment. The five Immune High patients undergoing primary cytoreductive surgery exhibited immune mobilization and extended progression-free survival, compared to the Immune Low patients undergoing the same treatment. Both laparoscopy and cytoreductive surgery induced substantial and transient changes in serum cytokines, with upregulation of the inflammatory cytokine IL-6 and downregulation of the multifunctional cytokines IP-10, Eotaxin, IL-4, and IL-7. Over the study period, cytokine levels uniformly decreased in all patients, leading to the elimination of the initial immune phenotypes regardless of treatment choice. This study reveals distinct pre-treatment immune phenotypes in HGSOC patients that might be informative for treatment stratification and prognosis. This potential novel biomarker holds promise as a foundation for improved assessment of treatment responses in patients with HGSOC. ClinicalTrials.gov Identifier: NCT03378297.
高等级浆液性卵巢癌患者治疗反应的新免疫表型
尽管手术和治疗方法不断进步,但高级别浆液性卵巢癌(HGSOC)的预后仍然很差。手术是治疗方案中不可或缺的组成部分,因为切除所有可见肿瘤病灶(细胞减灭术)可显著提高总生存率。加强评估细胞减灭术的预测工具对于优化治疗的精确性至关重要。患者的免疫状态广泛反映了肿瘤细胞的生物学行为以及患者对疾病和治疗的反应。血清细胞因子图谱是衡量免疫适应性和偏差的灵敏指标,但将其纳入治疗范例的研究还很欠缺。本研究是IMPACT试验(NCT03378297)的一部分,旨在描述HGSOC初治前和初治期间的免疫反应,以确定治疗选择和预后的生物标志物。该研究收集了22名患者从诊断到反应评估的纵向血清样本。根据腹腔镜检查评分,患者接受了原发囊肿切除手术或新辅助化疗(NACT)。用 Bio-Plex 200 分析的 27 种血清细胞因子显示了诊断时的两种免疫表型:免疫高,血清细胞因子水平明显高于免疫低。免疫表型反映了腹腔镜评分和手术治疗的分配。与接受同样治疗的免疫低下患者相比,接受初级细胞减灭术的五名免疫高患者表现出免疫动员和无进展生存期的延长。腹腔镜检查和细胞减灭术都会引起血清细胞因子的显著和短暂变化,炎性细胞因子IL-6上调,多功能细胞因子IP-10、Eotaxin、IL-4和IL-7下调。在研究期间,所有患者的细胞因子水平都一致下降,从而消除了最初的免疫表型,而与治疗选择无关。这项研究揭示了HGSOC患者治疗前的独特免疫表型,可能对治疗分层和预后有参考价值。这一潜在的新型生物标志物有望为改进 HGSOC 患者的治疗反应评估奠定基础。ClinicalTrials.gov Identifier:NCT03378297。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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