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J Pharm Health Care Sci. 2017 Jan 11;3:3. doi: 10.1186/s40780-016-0072-5. eCollection 2017.
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Recommendations for the Use of WBC Growth Factors: American Society of Clinical Oncology Clinical Practice Guideline Update.美国临床肿瘤学会临床实践指南更新:白细胞生长因子的应用建议。
J Clin Oncol. 2015 Oct 1;33(28):3199-212. doi: 10.1200/JCO.2015.62.3488. Epub 2015 Jul 13.
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Risk factors for febrile neutropenia among patients with cancer receiving chemotherapy: A systematic review.癌症化疗患者中性粒细胞减少性发热的危险因素:系统评价。
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Antiemetics: American Society of Clinical Oncology clinical practice guideline update.止吐药:美国临床肿瘤学会临床实践指南更新。
J Clin Oncol. 2011 Nov 1;29(31):4189-98. doi: 10.1200/JCO.2010.34.4614. Epub 2011 Sep 26.
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Guideline update for MASCC and ESMO in the prevention of chemotherapy- and radiotherapy-induced nausea and vomiting: results of the Perugia consensus conference.MASCC和ESMO预防化疗及放疗引起的恶心和呕吐指南更新:佩鲁贾共识会议结果
Ann Oncol. 2010 May;21 Suppl 5:v232-43. doi: 10.1093/annonc/mdq194.
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Dexamethasone reduces methotrexate biliary elimination and potentiates its hepatotoxicity in rats.地塞米松减少了甲氨蝶呤在大鼠胆汁中的消除,并增强了其肝毒性。
Toxicology. 2010 Jan 12;267(1-3):165-71. doi: 10.1016/j.tox.2009.11.010. Epub 2009 Nov 14.
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Evaluation of potential interaction between vinorelbine and clarithromycin.长春瑞滨与克拉霉素之间潜在相互作用的评估。
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Intensive anti-inflammatory therapy with dexamethasone in patients with non-small cell lung cancer: effect on chemotherapy toxicity and efficacy.地塞米松强化抗炎治疗对非小细胞肺癌患者化疗毒性及疗效的影响
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Steroid premedication markedly reduces liver and bone marrow toxicity of trabectedin in advanced sarcoma.在晚期肉瘤中,类固醇预处理可显著降低曲贝替定的肝脏和骨髓毒性。
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Glucocorticoid-induced granulocytosis: contribution of marrow release and demargination of intravascular granulocytes.糖皮质激素诱导的粒细胞增多症:骨髓释放及血管内粒细胞边缘池解除的作用
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地塞米松联合用药会增加接受甲氨蝶呤、长春碱、阿霉素和顺铂化疗的膀胱癌患者中性粒细胞减少的严重程度并加速其出现时间:一项回顾性队列研究。

Co-administration of dexamethasone increases severity and accelerates onset day of neutropenia in bladder cancer patients on methotrexate, vinblastine, adriamycin and cisplatin chemotherapy: a retrospective cohort study.

作者信息

Itai Shingo, Suga Yukio, Hara Yusuke, Izumi Kouji, Maeda Yuji, Kitagawa Yasuhide, Ishizaki Junko, Shimada Tsutomu, Mizokami Atsushi, Sai Yoshimichi

机构信息

Division of Life Sciences, Graduate School of Natural Science and Technology, Kanazawa University, Kakuma-machi, Kanazawa, 920-1192 Japan ; Department of Hospital Pharmacy, University Hospital, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8641 Japan.

Department of Clinical Drug Informatics, Faculty of Pharmacy, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kakuma-machi, Kanazawa, 920-1192 Japan.

出版信息

J Pharm Health Care Sci. 2017 Jan 11;3:3. doi: 10.1186/s40780-016-0072-5. eCollection 2017.

DOI:10.1186/s40780-016-0072-5
PMID:28097015
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5225533/
Abstract

BACKGROUND

Bladder cancer patients receiving methotrexate, vinblastine, adriamycin and cisplatin (MVAC) chemotherapy are co-administered with dexamethasone as an anti-emetic. We examined whether or not dexamethasone affects the severity and onset day of MVAC-induced severe neutropenia.

METHODS

This was a retrospective study of bladder cancer patients treated with MVAC chemotherapy with or without dexamethasone as an antiemetic at Kanazawa University Hospital during January 2005 - December 2009. Patients were categorized into three groups; no dexamethasone use (Dex (-)), dexamethasone on day 2 (Dex 1 day), and dexamethasone on days 2, 3 and 4 (Dex multiday). We evaluated the incidence of grade 3/4 neutropenia and the day of onset of first severe neutropenic episode during the first course of MVAC chemotherapy. Logistic regression was used to investigate whether co-administration of dexamethasone was a risk factor for severe neutropenia.

RESULTS

Episodes of grade 3/4 neutropenia occurred in 3 out of 6 (50.0%), 11 out of 12 (91.7%) and 6 out of 6 (100%) patients in the Dex (-), Dex 1 day, and Dex multiday groups, respectively. The appearance day of first severe neutropenia in the Dex multiday group (13.2 ± 1.0) was significantly accelerated compared to the Dex (-) group (17.7 ± 2.1). Univariate logistic regression analysis revealed that dexamethasone is a risk factor for severe neutropenia (OR 17.0; 95%CI: 1.3-223.1).

CONCLUSIONS

Co-administration of dexamethasone for anti-emesis brings forward the first appearance of neutropenia, and increases the severity of neutropenia, in bladder cancer patients receiving MVAC chemotherapy.

摘要

背景

接受甲氨蝶呤、长春花碱、阿霉素和顺铂(MVAC)化疗的膀胱癌患者会同时使用地塞米松作为止吐药。我们研究了地塞米松是否会影响MVAC诱导的严重中性粒细胞减少的严重程度和发生时间。

方法

这是一项对2005年1月至2009年12月在金泽大学医院接受MVAC化疗且使用或不使用地塞米松作为止吐药的膀胱癌患者的回顾性研究。患者分为三组:未使用地塞米松(Dex(-))、第2天使用地塞米松(Dex 1天)和第2、3、4天使用地塞米松(Dex多日)。我们评估了在MVAC化疗的第一个疗程中3/4级中性粒细胞减少的发生率以及首次严重中性粒细胞减少发作的发生时间。使用逻辑回归来研究地塞米松的联合使用是否是严重中性粒细胞减少的危险因素。

结果

Dex(-)组、Dex 1天组和Dex多日组中,3/4级中性粒细胞减少的发作分别发生在6例中的3例(50.0%)、12例中的11例(91.7%)和6例中的6例(100%)患者中。与Dex(-)组(17.7±2.1)相比,Dex多日组首次严重中性粒细胞减少的出现时间(13.2±1.0)明显提前。单因素逻辑回归分析显示,地塞米松是严重中性粒细胞减少的危险因素(OR 17.0;95%CI:1.3 - 223.1)。

结论

在接受MVAC化疗的膀胱癌患者中,联合使用地塞米松止吐会使中性粒细胞减少首次出现的时间提前,并增加中性粒细胞减少的严重程度。