小剂量泼尼松龙加醋酸阿比特龙治疗转移性阉割耐药前列腺癌引起的低钾血症的兼容性。

IF 1.2 Q4 PHARMACOLOGY & PHARMACY
Shota Torii, Aya Torii-Goto, Tamaki Tanizawa, Takashi Sakakibara, Ryosuke Oguri, Haruka Nagase, Yuri Nakao, Tomoyuki Hirashita, Kuniaki Tanaka, Norio Takimoto, Takahiro Hayashi
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引用次数: 0

摘要

研究背景本研究旨在调查低剂量泼尼松龙(PSL)与醋酸阿比特龙(abiraterone acetate,阿比特龙)加 PSL 联合疗法中低钾血症发生率之间的关系,研究对象为日本转移性耐阉割前列腺癌(mCRPC)患者:这项回顾性观察研究纳入了2014年9月至2022年10月期间在刈谷丰田综合医院和岐阜综合医疗中心接受阿比特龙和PSL治疗的153名mCRPC日本患者。比较了低剂量组(PSL 5 毫克/天)和标准剂量组(PSL 10 毫克/天)的≥2 级低钾血症发生率、血清钾水平变化以及持续联合治疗时间:本研究共纳入 153 例患者,其中 95 例为配对患者。低剂量组和标准剂量组分别有 13 名和 82 名患者。两组间≥2级低钾血症的发生率无明显差异[低剂量组为15.4%(2/13例患者),标准剂量组为12.2%(10/82例患者),P = 0.667]。低剂量组的血清钾水平从第 7 - 0 天的 4.63 降至第 84 ± 10 天的 4.16 mmol/L(n = 7,P = 0.066),而低剂量组从第 7 - 0 天到第 84 ± 10 天的血清钾水平似乎比标准剂量组高(n = 37,P = 0.475)。低剂量组(n = 13)和标准剂量组(n = 82,P = 0.427)阿比特龙和 PSL 治疗持续性的 Kaplan-Meier 曲线无显著差异:结论:日本mCRPC患者接受阿比特龙和5毫克/天PSL联合治疗不会改变≥2级低钾血症的发生率。不过,尽管不显著,但每天 5 毫克的 PSL 显示血清钾水平呈下降趋势,且变化程度大于每天 10 毫克的 PSL。因此,日本的 mCRPC 患者可以联合使用阿比特龙和每天 5 毫克的 PSL。必须通过测量血清钾水平和观察肌肉无力、抽搐等主观症状来监测患者是否出现低钾血症。此外,医生或药剂师必须向患者解释这些症状,并指示他们在出现这些症状时立即咨询医务人员。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Compatibility of hypokalaemia caused by low-dose prednisolone plus abiraterone acetate therapy for metastatic castration-resistant prostate cancer.

Background: This study aimed to investigate the relationship between low-dose prednisolone (PSL) and the incidence of hypokalaemia at abiraterone acetate (abiraterone) plus PSL combination therapy targeting Japanese patients with metastatic castration-resistant prostate cancer (mCRPC).

Methods: This retrospective observational study included 153 Japanese patients treated with abiraterone and PSL for mCRPC at Kariya Toyota General Hospital and Gifu General Medical Center between September 2014 and October 2022. The incidence of grade ≥ 2 hypokalaemia as well as serum potassium level variations and the continuous combination therapy duration were compared between the low-dose (5 mg/day of PSL) and the standard-dose (10 mg/day of PSL) groups.

Results: This study included 153 patient of which 95 were matched to establish the analysis population. The low-dose and the standard-dose groups consisted of 13 and 82 patients, respectively. No significant difference in the incidence of grade ≥ 2 hypokalaemia was observed between the two groups [15.4% (2/13 patients) in the low-dose group and 12.2% (10/82 patients) in the standard-dose group, P = 0.667]. The low-dose group exhibited a decrease in serum potassium levels from 4.63 on day - 7 - 0 to 4.16 mmol/L on day 84 ± 10 (n = 7, P = 0.066), and serum potassium levels from day - 7 - 0 to 84 ± 10 in the low-dose group appeared to be great in the standard-dose group (n = 37, P = 0.475). The Kaplan-Meier curves for continuity of abiraterone and PSL therapy were not significantly different between the low-dose group (n = 13) and standard-dose group (n = 82, P = 0.427).

Conclusion: Combination therapy with abiraterone and 5 mg/day of PSL in Japanese patients with mCRPC did not change the incidence of grade ≥ 2 hypokalaemia. However, although not significant, 5 mg/day of PSL demonstrated a decreasing trend in serum potassium levels with a larger degree of change than that of 10 mg/day of PSL. Therefore, the combination of abiraterone and 5 mg/day PSL can be administered to Japanese patients with mCRPC. The patients must be monitored for hypokalaemia through measurement of serum potassium levels and observation of subjective symptoms such as muscle weakness, convulsion etc. In addition, the doctor or the pharmacist must explain these symptoms to the patient and instruct them to consult their medical staff immediately in the event of development of such symptoms.

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