Itai Shingo, Suga Yukio, Hara Yusuke, Izumi Kouji, Maeda Yuji, Kitagawa Yasuhide, Ishizaki Junko, Shimada Tsutomu, Mizokami Atsushi, Sai Yoshimichi
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.
J Pharm Health Care Sci. 2017 Jan 11;3:3. doi: 10.1186/s40780-016-0072-5. eCollection 2017.
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.
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.
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).
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.
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。
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。
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)。
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。