Katsube Yurie, Hira Daiki, Tsujimoto Masayuki, Koide Hiroyoshi, Minegaki Tetsuya, Ikeda Yoshito, Morita Shin-Ya, Nishiguchi Kohshi, Terada Tomohiro
Int J Clin Pharmacol Ther. 2018 Jul;56(7):328-336. doi: 10.5414/CP203180.
Angiotensin receptor blockers (ARBs) are often used in patients on paclitaxel (PTX) and carboplatin combination (TC) therapy to treat hypertension caused by the co-administration of bevacizumab. The aim of this retrospective study was to analyze the association between co-administration of ARBs and the development of severe neutropenia in patients on TC therapy.
In this study, 211 concomitant medications were prescribed to 173 patients on TC therapy. 24 of those patients received ARBs. The incidences of neutropenia among those on various ARBs were compared.
Patients on candesartan cilexetil had the highest incidence of neutropenia compared to those on other concomitant medications, including other ARBs. Of 173 patients, 6 received candesartan cilexetil during the first cycle of TC therapy, and all 6 of them developed severe neutropenia. We noted that prior to TC therapy, there were no significant differences in age, serum albumin levels, neutrophil counts, liver injury marker, and renal function between the patients on candesartan cilexetil and those on other ARBs.
CONCLUSION: Our data suggest that a drug-drug interaction between candesartan cilexetil and TC therapy is probable. Unlike with other ARBs, the possible increased risk for development of severe neutropenia should be taken into account when prescribing candesartan cilexetil in combination with TC therapy. .
血管紧张素受体阻滞剂(ARBs)常用于接受紫杉醇(PTX)和卡铂联合(TC)治疗的患者,以治疗因同时使用贝伐单抗引起的高血压。这项回顾性研究的目的是分析在接受TC治疗的患者中,ARBs的联合使用与严重中性粒细胞减少症发生之间的关联。
在本研究中,为173例接受TC治疗的患者开具了211种伴随用药。其中24例患者接受了ARBs治疗。比较了使用各种ARBs的患者中性粒细胞减少症的发生率。
与包括其他ARBs在内的其他伴随用药相比,服用坎地沙坦酯的患者中性粒细胞减少症的发生率最高。在173例患者中,有6例在TC治疗的第一个周期接受了坎地沙坦酯治疗,他们全部发生了严重中性粒细胞减少症。我们注意到,在TC治疗之前,服用坎地沙坦酯的患者与服用其他ARBs的患者在年龄、血清白蛋白水平、中性粒细胞计数、肝损伤标志物和肾功能方面没有显著差异。
我们的数据表明,坎地沙坦酯与TC治疗之间可能存在药物相互作用。与其他ARBs不同,在将坎地沙坦酯与TC治疗联合使用时,应考虑到发生严重中性粒细胞减少症的风险可能增加。