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既往治疗如何改变转移性乳腺癌患者的代谢组学特征。

How previous treatment changes the metabolomic profile in patients with metastatic breast cancer.

机构信息

Department of Gynecology and Obstetrics, University of Heidelberg, Im Neuenheimer Feld 440, 69120, Heidelberg, Germany.

BIOCRATES Life Sciences AG, 6020, Innsbruck, Austria.

出版信息

Arch Gynecol Obstet. 2022 Dec;306(6):2115-2122. doi: 10.1007/s00404-022-06558-5. Epub 2022 Apr 25.

Abstract

PURPOSE

Metabolites are in the spotlight of attention as promising novel breast cancer biomarkers. However, no study has been conducted concerning changes in the metabolomics profile of metastatic breast cancer patients according to previous therapy.

METHODS

We performed a retrospective, single-center, nonrandomized, partially blinded, treatment-based study. Metastatic breast cancer (MBC) patients were enrolled between 03/2010 and 09/2016 at the beginning of a new systemic therapy. The endogenous metabolites in the plasma samples were analyzed using the AbsoluteIDQ p180 Kit (Biocrates Life Sciences AG, Innsbruck) a targeted, quality and quantitative-controlled metabolomics approach. The statistical analysis was performed using R package, version 3.3.1. ANOVA was used to statistically assess age differences within groups. Furthermore, we analyzed the CTC status of the patients using the CellSearch assay.

RESULTS

We included 178 patients in our study. Upon dividing the study population according to therapy before study inclusion, we found the following: 4 patients had received no therapy, 165 chemotherapy, and 135 anti-hormonal therapy, 30 with anti-Her2 therapy and 38 had received treatment with bevacizumab. Two metabolites were found to be significantly different, depending on the further therapy of the patients: methionine and serine. Whereas methionine levels were higher in the blood of patients who received an anti-Her2-therapy, serine was lower in patients with endocrine therapy only.

CONCLUSION

We identified two metabolites for which concentrations differed significantly depending on previous therapies, which could help to choose the next therapy in patients who have already received numerous different treatments.

摘要

目的

代谢物作为有前途的新型乳腺癌生物标志物备受关注。然而,尚无研究针对既往治疗的转移性乳腺癌(MBC)患者代谢组学谱的变化。

方法

我们进行了一项回顾性、单中心、非随机、部分盲法、基于治疗的研究。2010 年 3 月至 2016 年 9 月,在开始新的全身治疗时,MBC 患者入组。使用 AbsoluteIDQ p180 试剂盒(Biocrates Life Sciences AG,因斯布鲁克)分析血浆样本中的内源性代谢物,这是一种靶向、质量和定量控制的代谢组学方法。使用 R 包(版本 3.3.1)进行统计分析。ANOVA 用于统计评估组内年龄差异。此外,我们使用 CellSearch 检测分析了患者的 CTC 状态。

结果

我们的研究纳入了 178 例患者。根据研究纳入前的治疗情况对研究人群进行分组,我们发现:4 例患者未接受治疗,165 例接受化疗,135 例接受抗激素治疗,30 例接受抗 Her2 治疗,38 例接受贝伐单抗治疗。有两种代谢物的浓度根据患者的进一步治疗而有显著差异:蛋氨酸和丝氨酸。接受抗 Her2 治疗的患者血液中的蛋氨酸水平较高,而仅接受内分泌治疗的患者丝氨酸水平较低。

结论

我们发现了两种代谢物,其浓度根据既往治疗有显著差异,这可能有助于为已经接受了多种不同治疗的患者选择下一种治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6c4/9633507/5f0588f20000/404_2022_6558_Fig1_HTML.jpg

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