Meloxicam as an adjuvant to peginterferon-α-2a and ribavirin treatment for genotype 1 chronic hepatitis C: A randomized trial

被引:0
作者
Kagawa, Tatehiro [1 ]
Kojima, Sei-ichiro [2 ]
Shiraishi, Koichi [1 ]
Hirose, Shunji [1 ]
Arase, Yoshitaka [1 ]
Takashimizu, Shinji [2 ]
Watanabe, Norihito [2 ]
Nagata, Naruhiko [3 ]
Numata, Makoto [3 ]
Shiozawa, Hirokazu [4 ]
Nishizaki, Yasuhiro [4 ]
Toki, Mayu [5 ]
Sugita, Teruji [5 ]
Nomura, Kijuro [6 ]
Sakaguchi, Takashi [7 ]
Atsukawa, Kazuhiro [7 ]
Tajima, Hiroto [8 ]
Tei, Yoshihiro [8 ]
Inomoto, Tsutomu [9 ]
Mine, Tetsuya [1 ]
机构
[1] Tokai Univ, Sch Med, Dept Internal Med, Div Gastroenterol, Isehara, Kanagawa 2591193, Japan
[2] Tokai Univ, Hachioji Hosp, Dept Internal Med, Div Gastroenterol, Hachioji, Tokyo, Japan
[3] Tokai Univ, Oiso Hosp, Dept Internal Med, Div Gastroenterol, Nakagun, Japan
[4] Tokai Univ, Tokyo Hosp, Dept Internal Med, Div Gastroenterol, Tokyo 151, Japan
[5] Yamachika Mem Hosp, Odawara, Japan
[6] Nomura Shokakinaika, Chigasaki, Kanagawa, Japan
[7] Hiratsuka City Hosp, Hiratsuka, Kanagawa, Japan
[8] Japan Med Alliance Ebina Gen Hosp, Ebina, Kanagawa, Japan
[9] Yugawara Kosei Nenkin Hosp, Ashigarashimogun, Japan
关键词
adjuvant; chronic hepatitis C; cyclooxygenase-2; inhibitor; interferon; meloxicam; neutropenia; NONSTEROIDAL ANTIINFLAMMATORY DRUG; PEGYLATED-INTERFERON-ALPHA; VIROLOGICAL RESPONSE; VIRUS-INFECTION; PLUS RIBAVIRIN; THERAPY; COMBINATION; KETOPROFEN; CYCLOOXYGENASE-2; TELAPREVIR;
D O I
10.1111/hepr.12046
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim: In this multicenter, randomized trial, we evaluated the effectiveness of meloxicam - a non-steroidal anti-inflammatory drug - as an adjuvant for enhancing antiviral efficacy and preventing neutropenia during the treatment of patients with genotype 1 chronic hepatitis C using peginterferon and ribavirin. Methods: A total of 60 patients were randomly assigned, in a 1:1 ratio, to either the meloxicam or the control group after stratification by neutrophil count. Both groups received weekly peginterferon-alpha-2a (180g) and a weight-based dose of ribavirin for 48 weeks. The meloxicam group received meloxicam (10mg/day) for the first 8 weeks after initiation of treatment. Results: Through intent-to-treat analysis, we found that the sustained virological response rate in the meloxicam group (19/30, 63.3%) was significantly higher than in the control group (11/30, 36.7%, P<0.05). The relapse rate was more than twice as high (45%) in the control group than in the meloxicam group (19.0%); however, this difference was not statistically significant. The rate of neutrophil decrease, calculated by dividing the lowest value observed during the first 8 weeks by pretreatment count, was significantly smaller in the meloxicam group (55.1 +/- 14.3%) than in the control group (62.3 +/- 9.6%, P<0.05). Conclusion: Meloxicam enhanced antiviral efficacy and reduced the decline in neutrophil counts for the peginterferon and ribavirin treatment of genotype 1 chronic hepatitis C. This drug could be a reasonable adjuvant for the treatment of patients with chronic hepatitis C. The present study including a small number of patients warrants larger clinical trials.
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页码:925 / 932
页数:8
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