Evaluation of a blood miRNA/mRNA signature to follow-up Lu-PRRT therapy for G1/G2 intestinal neuroendocrine tumors

Virginie Jacques, L. Dierickx, J. Texier, S. Brillouet, Frédéric Courbon, Rosine Guimbaud, Lavinia Vija, Frédérique Savagner
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Abstract

177Lu-oxodotreotide peptide receptor therapy (LuPRRT) is an efficient treatment for midgut neuroendocrine tumors (NETs) of variable radiological response. Several clinical, biological, and imaging parameters may be used to establish a relative disease prognosis but none is able to predict early efficacy or toxicities. We investigated expression levels for mRNA and miRNA involved in radiosensitivity and tumor progression searching for correlations related to patient outcome during LuPRRT therapy.Thirty-five patients received LuPRRT for G1/G2 midgut NETs between May 2019 and September 2021. Peripheral blood samples were collected prior to irradiation, before and 48 h after the second and the fourth LuPRRT, and at 6-month follow-up. Multiple regression analyses and Pearson correlations were performed to identify the miRNA/mRNA signature that will best predict response to LuPRRT.Focusing on four mRNAs and three miRNAs, we identified a miRNA/mRNA signature enabling the early identification of responders to LuPRRT with significant reduced miRNA/mRNA expression after the first LuPRRT administration for patients with progressive disease at 1 year (p < 0.001). The relevance of this signature was reinforced by studying its evolution up to 6 months post-LuPRRT. Moreover, nadir absolute lymphocyte count within the first 2 months after the first LuPRRT administration was significantly related to low miRNA/mRNA expression level (p < 0.05) for patients with progressive disease.We present a pilot study exploring a miRNA/mRNA signature that correlates with early hematologic toxicity and therapeutic response 12 months following LuPRRT. This signature will be tested prospectively in a larger series of patients.
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评估血液 miRNA/mRNA特征,以跟踪 Lu-PRRT 治疗 G1/G2 肠神经内分泌肿瘤的情况
177Lu-oxodotreotide 肽受体疗法(LuPRRT)是治疗放射性反应不一的中肠神经内分泌肿瘤(NET)的有效方法。一些临床、生物和成像参数可用于确定疾病的相对预后,但没有一个参数能预测早期疗效或毒性。2019年5月至2021年9月期间,35名G1/G2中肠NET患者接受了LuPRRT治疗。在照射前、第二次和第四次LuPRRT之前和之后48小时以及随访6个月时收集外周血样本。通过多元回归分析和皮尔逊相关性分析,我们确定了一个miRNA/mRNA特征,该特征能早期识别对LuPRRT有反应的患者,在首次LuPRRT给药后1年,疾病进展期患者的miRNA/mRNA表达显著降低(p < 0.001)。通过研究该特征在LuPRRT治疗后6个月内的变化情况,进一步证实了该特征的相关性。此外,对于疾病进展期患者来说,首次使用 LuPRRT 后 2 个月内的绝对淋巴细胞计数最低值与低 miRNA/mRNA 表达水平显著相关(p < 0.05)。该特征将在更大范围的患者中进行前瞻性测试。
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