Wakasugi Yoshinori, Noda Satoshi, Ikuno Yoshihiro, Horie Miya, Kito Katsuyuki, Minamiguchi Hitoshi, Terada Tomohiro
1Department of Pharmacy, Shiga University of Medical Science Hospital, 520-2192 Seta Tsukinowa-cho, Otsu-shi, Shiga Japan.
2Department of Hematology, Shiga University of Medical Science Hospital, 520-2192 Seta Tsukinowa-cho, Otsu-shi, Shiga Japan.
J Pharm Health Care Sci. 2019 Nov 21;5:24. doi: 10.1186/s40780-019-0153-3. eCollection 2019.
Cyclophosphamide, doxorubicin, vincristine, and prednisolone (CHOP) regimen includes a high dose of prednisolone (100 mg/body), which exhibits an anticancer and antiemetic effect. However, its optimal use for antiemetic therapy has not been established yet. We assessed the efficacy of granisetron plus aprepitant versus granisetron for CHOP or rituximab-CHOP (R-CHOP) regimen-induced nausea and vomiting in malignant lymphoma.
This retrospective and observational clinical study included patients who received CHOP or R-CHOP regimen as initiating chemotherapy between July 2010 and March 2016 ( = 39). Patients were assigned to an aprepitant [aprepitant (125 mg on day 1, 80 mg on days 2-3) plus granisetron (3 mg); = 15] or control regimen group [granisetron (3 mg); = 24]. Complete response (CR), defined as no vomiting and no use of rescue therapy during overall phase (0-120 h), was the primary endpoint. Secondary endpoints included the time to first vomiting and using rescue medication and complete protection (CP) defined as no vomiting and no retching and/or no nausea and no rescue therapy. The patient records were investigated, and data were retrospectively analyzed.
CR rate CP rates did not significantly differ between the groups during the observation period (80.0% versus 83.3%, = 1.000; and 80.0% versus 79.2%, = 1.000, respectively). Additionally, the time to first vomiting and using rescue medication in did not significantly differ between the groups ( = 0.909).
This study suggests that granisetron alone could be one treatment option in the management of CINV in patients with non-Hodgkin lymphoma receiving CHOP or R-CHOP regimen.
环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP)方案包含高剂量泼尼松龙(100毫克/体质量),具有抗癌和止吐作用。然而,其在止吐治疗中的最佳应用尚未确立。我们评估了格拉司琼联合阿瑞匹坦与格拉司琼单药治疗CHOP或利妥昔单抗-CHOP(R-CHOP)方案所致恶性淋巴瘤恶心和呕吐的疗效。
这项回顾性观察性临床研究纳入了2010年7月至2016年3月期间接受CHOP或R-CHOP方案作为初始化疗的患者(n = 39)。患者被分为阿瑞匹坦组[阿瑞匹坦(第1天125毫克,第2 - 3天80毫克)加格拉司琼(3毫克);n = 15]或对照组[格拉司琼(3毫克);n = 24]。完全缓解(CR)定义为在整个阶段(0 - 120小时)无呕吐且未使用解救治疗,是主要终点。次要终点包括首次呕吐时间、使用解救药物时间以及完全保护(CP),CP定义为无呕吐、无干呕和/或无恶心且未使用解救治疗。对患者记录进行调查,并对数据进行回顾性分析。
观察期内两组的CR率和CP率无显著差异(分别为80.0%对83.3%,P = 1.000;80.0%对79.2%,P = 1.000)。此外,两组首次呕吐时间和使用解救药物时间无显著差异(P = 0.909)。
本研究表明,对于接受CHOP或R-CHOP方案的非霍奇金淋巴瘤患者,单独使用格拉司琼可能是管理化疗引起的恶心和呕吐的一种治疗选择。