Wong Chi Wah, Yost Susan E, Lee Jin Sun, Gillece John D, Folkerts Megan, Reining Lauren, Highlander Sarah K, Eftekhari Zahra, Mortimer Joanne, Yuan Yuan
Department of Applied AI and Data Science, City of Hope National Medical Center, Duarte, CA, United States.
Department of Medical Oncology & Therapeutic Research, City of Hope National Medical Center, Duarte, CA, United States.
Front Oncol. 2021 Mar 10;11:604584. doi: 10.3389/fonc.2021.604584. eCollection 2021.
Neratinib has great efficacy in treating HER2+ breast cancer but is associated with significant gastrointestinal toxicity. The objective of this pilot study was to understand the association of gut microbiome and neratinib-induced diarrhea. Twenty-five patients (age ≥ 60) were enrolled in a phase II trial evaluating safety and tolerability of neratinib in older adults with HER2+ breast cancer (NCT02673398). Fifty stool samples were collected from 11 patients at baseline and during treatment. 16S rRNA analysis was performed and relative abundance data were generated. Shannon's diversity was calculated to examine gut microbiome dysbiosis. An explainable tree-based approach was utilized to classify patients who might experience neratinib-related diarrhea (grade ≥ 1) based on pre-treatment baseline microbial relative abundance data. The hold-out Area Under Receiver Operating Characteristic and Area Under Precision-Recall Curves of the model were 0.88 and 0.95, respectively. Model explanations showed that patients with a larger relative abundance of 9 and sp. HPS0048 may have reduced risk of neratinib-related diarrhea and was confirmed by Kruskal-Wallis test (p ≤ 0.05, uncorrected). Our machine learning model identified microbiota associated with reduced risk of neratinib-induced diarrhea and the result from this pilot study will be further verified in a larger study.
ClinicalTrials.gov, identifier NCT02673398.
奈拉替尼在治疗HER2阳性乳腺癌方面具有显著疗效,但会引发严重的胃肠道毒性。本初步研究的目的是了解肠道微生物群与奈拉替尼所致腹泻之间的关联。25名年龄≥60岁的患者参与了一项II期试验,评估奈拉替尼在HER2阳性老年乳腺癌患者中的安全性和耐受性(NCT02673398)。在基线期和治疗期间从11名患者中收集了50份粪便样本。进行了16S rRNA分析并生成了相对丰度数据。计算香农多样性以检查肠道微生物群失调情况。采用一种基于可解释树的方法,根据治疗前基线微生物相对丰度数据对可能发生奈拉替尼相关腹泻(≥1级)的患者进行分类。该模型的留一法受试者操作特征曲线下面积和精确召回率曲线下面积分别为0.88和0.95。模型解释表明,相对丰度较高的9和sp. HPS0048的患者发生奈拉替尼相关腹泻的风险可能降低,这一点通过Kruskal-Wallis检验得到了证实(p≤0.05,未校正)。我们的机器学习模型识别出了与奈拉替尼所致腹泻风险降低相关的微生物群,本初步研究的结果将在更大规模的研究中进一步验证。
ClinicalTrials.gov,标识符NCT02673398。