Division of Hematology-Oncology, Department of Internal Medicine, Gyeongsang National University Changwon Hospital, Gyeongsang National University School of Medicine, Changwon, Republic of Korea.
Division of Hematology/Oncology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Oncologist. 2017 Nov;22(11):1354-1361. doi: 10.1634/theoncologist.2017-0129. Epub 2017 Jul 7.
To assess whether the rotation of dexamethasone to methylprednisolone decreases the intensity of dexamethasone-induced hiccup (DIH) in cancer patients treated with chemotherapy.
Adult patients who experienced DIH within 3 days after the administration of dexamethasone as an antiemetic were screened. Eligible patients were randomly assigned to receive dexamethasone ( = 33) or methylprednisolone ( = 32) as an antiemetic (randomization phase). In the next cycle of chemotherapy, the dexamethasone group received methylprednisolone and vice versa in the methylprednisolone group (crossover phase). The primary endpoint was the difference in hiccup intensity as measured using the numeric rating scale (NRS) between two groups.
No female patients were enrolled, although the study did not exclude them. At the randomization phase, hiccup frequency was 28/33 (84.8%) in the dexamethasone group versus 20/32 (62.5%) in the methylprednisolone group ( = .04). Intensity of hiccup was significantly higher in the dexamethasone group than that in the methylprednisolone group (mean NRS, 3.5 vs. 1.4, < .001). At the crossover phase, hiccup intensity was further decreased after the rotation of dexamethasone to methylprednisolone in the dexamethasone group (mean NRS, 3.5 to 0.9, < .001), while it was increased by rotating methylprednisolone to dexamethasone in the methylprednisolone group (mean NRS, 1.4 to 3.3, = .025). There were no differences in emesis intensity between the two groups at either the randomization or crossover phases. Clinicaltrials.gov identifier: NCT01974024.
Dexamethasone-induced hiccup is a male-predominant phenomenon that can be ameliorated by rotating dexamethasone to methylprednisolone without compromising the antiemetic efficacy.
In this randomized, multicenter, phase III trial, hiccup intensity was significantly lower when the antiemetic corticosteroid was rotated from dexamethasone to methylprednisolone without a change in emesis intensity than that when dexamethasone was maintained. At the crossover phase, hiccup intensity was increased again if dexamethasone was readministered instead of methylprednisolone. The present study demonstrated that dexamethasone-induced hiccup can be improved by rotating from dexamethasone to methylprednisolone without compromising its antiemetic efficacy.
评估地塞米松转换为甲泼尼龙是否会降低接受化疗的癌症患者中地塞米松引起的呃逆(DIH)的强度。
筛选出在接受地塞米松作为止吐药后 3 天内发生 DIH 的成年患者。符合条件的患者被随机分配接受地塞米松(=33)或甲泼尼龙(=32)作为止吐药(随机分组阶段)。在下一个化疗周期中,地塞米松组接受甲泼尼龙,而甲泼尼龙组接受地塞米松(交叉分组阶段)。主要终点是两组之间使用数字评分量表(NRS)测量的呃逆强度差异。
尽管该研究没有排除女性患者,但没有纳入女性患者。在随机分组阶段,地塞米松组呃逆频率为 28/33(84.8%),而甲泼尼龙组为 20/32(62.5%)( = .04)。地塞米松组呃逆强度明显高于甲泼尼龙组(平均 NRS,3.5 对 1.4, < .001)。在交叉分组阶段,地塞米松组将地塞米松转换为甲泼尼龙后,呃逆强度进一步降低(平均 NRS,3.5 至 0.9, < .001),而甲泼尼龙组将甲泼尼龙转换为地塞米松后,呃逆强度增加(平均 NRS,1.4 至 3.3, = .025)。两组在随机分组或交叉分组阶段的呕吐强度均无差异。Clinicaltrials.gov 标识符:NCT01974024。
地塞米松引起的呃逆是一种男性为主的现象,可以通过将地塞米松转换为甲泼尼龙来改善,而不会影响止吐效果。
在这项随机、多中心、三期试验中,与保持地塞米松不变相比,将止吐皮质类固醇从地塞米松转换为甲泼尼龙时,呃逆强度显著降低,而呕吐强度无变化。在交叉分组阶段,如果重新给予地塞米松而不是甲泼尼龙,则呃逆强度再次增加。本研究表明,通过将地塞米松转换为甲泼尼龙而不影响其止吐作用,可以改善地塞米松引起的呃逆。