Double-blind, placebo-controlled, randomized phase II study of TJ-14 (hangeshashinto) for gastric cancer chemotherapy-induced oral mucositis

被引:34
作者
Aoyama, Toru [1 ]
Nishikawa, Kazuhiro [2 ]
Takiguchi, Nobuhiro [3 ]
Tanabe, Kazuaki [4 ]
Imano, Motohiro [5 ]
Fukushima, Ryoji [6 ]
Sakamoto, Junichi [7 ]
Oba, Mari S. [8 ]
Morita, Satoshi [8 ]
Kono, Toru [9 ]
Tsuburaya, Akira [10 ]
机构
[1] Miura City Hosp, Dept Surg, Miura, Kanagawa, Japan
[2] Osaka Gen Med Ctr, Dept Surg, Osaka, Japan
[3] Chiba Canc Ctr, Dept Surg Gastroenterol, Chiba 2608717, Japan
[4] Hiroshima Univ, Dept Gastroenterol & Transplant Surg, Hiroshima, Japan
[5] Kinki Univ, Fac Med, Dept Surg, Osaka, Japan
[6] Teikyo Univ, Sch Med, Dept Surg, Tokyo 173, Japan
[7] Tokai Cent Hosp, Kakamigahara, Japan
[8] Yokohama City Univ, Dept Biostat & Epidemiol, Yokohama, Kanagawa 232, Japan
[9] Sapporo Higashi Tokushukai Hosp, Adv Surg Ctr, Sapporo, Hokkaido, Japan
[10] Shonan Kamakura Gen Hosp, Kamakura, Kanagawa, Japan
关键词
Oral mucositis; Hangeshashinto (TJ-14); Chemotherapy; Gastric cancer; HANGE-SHASHIN-TO; SMALL-INTESTINAL MUCOSA; PROSTAGLANDIN E-2; CYCLOOXYGENASE-2; EXPRESSION; ACUTE ENDOTOXEMIA; COX-2; WATER-ABSORPTION; KAMPO MEDICINE; RAT; MACROPHAGES;
D O I
10.1007/s00280-014-2440-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hangeshashinto (TJ-14, a Kampo medicine), which reduces the level of prostaglandin E2 and affects the cyclooxygenase activity, alleviates chemotherapy-induced oral mucositis (COM). We conducted a randomized comparative trial to investigate whether TJ-14 prevents and controls COM in patients with gastric cancer. We randomly assigned patients with gastric cancer who developed moderate-to-severe oral mucositis (CTCAE v4.0 grade a parts per thousand 1) during any cycle of chemotherapy to receive either TJ-14 or a placebo as a double-blind trial. The patients received a placebo or TJ-14 for 2-6 weeks according to the chemotherapy regimen from the beginning of the next course of chemotherapy. The primary end point was the incidence of grade a parts per thousand 2 oral mucositis in the protocol treatment course, and the secondary end points were the time to disappearance of oral mucositis and the incidence of adverse events. Following the key opening of the blinding protocol, we analyzed 91 eligible patients (TJ-14: 45, placebo: 46) using a "per protocol set" analysis. The incidence of a parts per thousand grade 2 COM was 40.0 % in the TJ-14 group and 41.3 % in the placebo group (p = 0.588). The median duration of a parts per thousand grade 2 COM was 14 days in the TJ-14 group and 16 days in the placebo group (p = 0.894). Meanwhile, the median duration of any grade of COM was 9 days in the TJ-14 group and 17 days in the placebo group among the patients who developed grade 1 symptoms during the screening cycle [hazard ratio 0.60; 95 % CI (0.23-1.59), p = 0.290]. Although TJ-14 treatment did not reduce the incidence of a parts per thousand yen2 COM in the patients who developed mucositis during chemotherapy for gastric cancer, a trend was observed in which TJ-14 reduced the risk of COM in the patients who developed grade 1 COM during the screening cycle. Further, phase III studies with a larger sample size are needed to clarify the protective effects of TJ-14 for COM.
引用
收藏
页码:1047 / 1054
页数:8
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