Miyata Yoshiharu, Yakushijin Kimikazu, Inui Yumiko, Imamura Yoshinori, Goto Hideaki, Mizutani Yu, Kurata Keiji, Kakiuchi Seiji, Sanada Yukinari, Minami Yosuke, Kawamoto Shinichiro, Yamamoto Katsuya, Ito Mitsuhiro, Tominaga Ryo, Gomyo Hiroshi, Mizuno Ishikazu, Nomura Tetsuhiko, Kitagawa Koichi, Sugimoto Takeshi, Murayama Tohru, Matsuoka Hiroshi, Minami Hironobu
Division of Medical Oncology/Hematology, Department of Medicine, Kobe University Hospital, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan.
Division of Oncology, Kobe Minimally Invasive Cancer Center, Kobe, Japan.
Int J Hematol. 2016 Dec;104(6):682-691. doi: 10.1007/s12185-016-2089-9. Epub 2016 Sep 9.
To identify strategies for reducing emesis induced by the CHOP regimen, which includes high-dose steroids, we prospectively evaluated the efficacy of palonosetron in Japanese patients. Palonosetron was administered at a dose of 0.75 mg via intravenous injection over 30 min before chemotherapy on day 1. Patients kept diaries of chemotherapy-induced nausea and vomiting (CINV) incidence from the start of chemotherapy until 168 h afterwards, in which they documented the occurrence and severity of nausea, vomiting, anorexia, and the use of rescue medication. The primary endpoint was the overall occurrence rate of nausea, vomiting, and anorexia; these rates were 56, 12, and 62 %, respectively, including all grades. The rates and severity of symptoms tended to worsen 120-168 h after completing oral prednisolone. We defined complete response (CR) as no vomiting and no use of rescue therapy. The CR rates of post palonosetron 0.75 mg treatment in the acute (0-24 h), delayed (24-168 h), and overall phases (0-168 h) were 86, 66, and 62 %, respectively. Antiemetic strategies of CHOP regimen for day 6 and, thereafter, should be investigated.
为了确定减少包含大剂量类固醇的CHOP方案所致呕吐的策略,我们前瞻性地评估了帕洛诺司琼在日本患者中的疗效。在第1天化疗前30分钟,通过静脉注射以0.75毫克的剂量给予帕洛诺司琼。患者记录从化疗开始至之后168小时化疗引起的恶心和呕吐(CINV)发生率,记录恶心、呕吐、厌食的发生情况和严重程度以及救援药物的使用情况。主要终点是恶心、呕吐和厌食的总体发生率;包括所有级别,这些发生率分别为56%、12%和62%。在完成口服泼尼松龙后120 - 168小时,症状的发生率和严重程度往往会加重。我们将完全缓解(CR)定义为无呕吐且未使用救援治疗。帕洛诺司琼0.75毫克治疗后在急性(0 - 24小时)、延迟(24 - 168小时)和总体阶段(0 - 168小时)的CR率分别为86%、66%和62%。应研究第6天及之后CHOP方案的止吐策略。