RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A retrospective investigation of the relationship between neuroblastoma response to anti-GD2 monoclonal antibodies and exposure to opioids for pain management.
A retrospective investigation of the relationship between neuroblastoma response to anti-GD2 monoclonal antibodies and exposure to opioids for pain management.
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我们的研究未发现阿片类药物消耗量与自然杀伤(NK)细胞介导的 NB 细胞杀伤(以对肿瘤体积/肿瘤负荷的影响衡量)之间存在统计学显著相关性。
近期对阿片类药物暴露的关注和研究增加,提示其可能与癌症结局相关。神经母细胞瘤(NB)儿童常需使用阿片类药物镇痛,但临床上尚未研究肿瘤对化疗的应答与阿片暴露之间的关联。
本研究回顾单一机构2013至2016年接受治疗的NB患者。研究根据抗体输注期间护士控制或患者自控镇痛记录,以吗啡等效剂量(mg/kg)量化阿片类药物使用,并分析其与原发肿瘤体积变化和总肿瘤负荷的关系。
42例因接受抗双唾液酸神经节苷脂单克隆抗体(抗GD2 mAb)而使用阿片类药物镇痛的患者中,36例数据完整并纳入统计分析。8天内按体重校正的吗啡等效剂量中位数为4.71 mg/kg(四分位距3.49–7.96)。总吗啡等效剂量与肿瘤体积比之间呈弱负相关,但无统计学意义(相关系数−0.0103,p=0.9525);与Curie评分比之间呈弱正相关,也无统计学意义(相关系数0.1096,p=0.5247)。
本研究未发现阿片类药物用量与NK细胞介导的NB细胞杀伤之间存在统计学显著相关性;后者依据肿瘤体积和肿瘤负荷变化衡量。
Recent increased awareness and research studies reflect possible associations between opioid exposure and cancer outcomes. Children with neuroblastoma (NB) often require opioid treatment for pain. However, associations between tumor response to chemotherapy and opioid exposure have not been investigated in clinical settings.
This is a single-institution retrospective review of patients with NB treated between 2013 and 2016. We evaluated opioid consumption quantified in morphine equivalent doses (mg/kg) based on nurse- or patient-controlled analgesia during antibody infusions. We also analyzed their associations with change in primary tumor volume and total tumor burden.
Of 42 patients given opioids for pain related to anti-disialoganglioside monoclonal antibodies (anti-GD2 mAb), data completion was achieved for 36, and details of statistical analyses were entered. Median total weight-based morphine equivalent (over 8 days) was 4.71 mg/kg (interquartile range 3.49-7.96). We found a statistically insignificant weak negative relationship between total weight-based morphine equivalents and tumor volume ratio (correlation coefficient -.0103, p-value .9525) and a statistically insignificant weak positive relationship between total weight-based morphine equivalent and Curie score ratio (correlation coefficient .1096, p-value .5247).
Our study found no statistically significant correlation between opioid consumption and natural killer (NK) cell-mediated killing of NB cells as measured by effects on tumor volume/tumor load.
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