Takashima Shuichiro, Eto Tetsuya, Shiratsuchi Motoaki, Hidaka Michihiro, Mori Yasuo, Kato Koji, Kamezaki Kenjiro, Oku Seido, Henzan Hideho, Takase Ken, Matsushima Takamitsu, Takenaka Katsuto, Iwasaki Hiromi, Miyamoto Toshihiro, Akashi Koichi, Teshima Takanori
Department of Medicine and Biosystemic Science, Graduate School of Medical Sciences, Kyushu University, Japan.
Intern Med. 2014;53(12):1315-20. doi: 10.2169/internalmedicine.53.1858. Epub 2014 Jun 15.
We examined the therapeutic strategies for treating mild gastrointestinal (GI) graft-versus-host disease (GVHD) using oral beclomethasone dipropionate (BDP) in 15 Japanese patients based on the donor source. The primary objective was to determine the efficacy and toxicity of oral BDP combined with/without low-dose prednisone (PSL).
Oral BDP was administered with 1 mg/kg/d of PSL in patients undergoing bone marrow transplantation (BMT) or peripheral blood stem cell transplantation (PBSCT; n=11), and the dose of PSL was tapered off after 22 days. Oral BDP alone was administered in patients undergoing cord blood stem cell transplantation (CBSCT; n=4). The primary endpoint was the rate of treatment success on day 49, as measured according to the improvement or complete resolution of GI symptoms without additional treatment. The secondary endpoints included treatment-related toxicity according to the National Cancer Institute Common Toxicity Criteria version 3.0, the rate of treatment discontinuation due to toxicity, the rate of relapse of acute GVHD by day 100 and the incidence of bacterial, fungal or viral infection, including cytomegalovirus (CMV) antigenemia.
Treatment success was achieved in seven of the 11 (64%) patients undergoing BMT or PBSCT and in all four patients (100%) undergoing CBSCT. Subsequent adverse events included herpes zoster infection, catheter-associated sepsis and CMV enteritis; all affected patients responded well to treatment.
The use of a risk-stratified treatment strategy with oral BDP depending on the stem cell source is effective in patients with mild GI-GVHD.
我们基于供体来源,对15例日本患者使用口服二丙酸倍氯米松(BDP)治疗轻度胃肠道移植物抗宿主病(GVHD)的治疗策略进行了研究。主要目的是确定口服BDP联合/不联合低剂量泼尼松(PSL)的疗效和毒性。
接受骨髓移植(BMT)或外周血干细胞移植(PBSCT;n = 11)的患者,口服BDP并联合1mg/kg/d的PSL,22天后逐渐减少PSL剂量。接受脐血干细胞移植(CBSCT;n = 4)的患者单独口服BDP。主要终点是第49天的治疗成功率,根据胃肠道症状改善或完全缓解且无需额外治疗来衡量。次要终点包括根据美国国立癌症研究所通用毒性标准第3.0版评估的治疗相关毒性、因毒性导致的治疗中断率、第100天急性GVHD的复发率以及细菌、真菌或病毒感染的发生率,包括巨细胞病毒(CMV)血症。
接受BMT或PBSCT的11例患者中有7例(64%)治疗成功,接受CBSCT的所有4例患者(100%)治疗成功。随后的不良事件包括带状疱疹感染、导管相关败血症和CMV肠炎;所有受影响患者对治疗反应良好。
根据干细胞来源采用口服BDP的风险分层治疗策略对轻度胃肠道GVHD患者有效。