{"title":"口服二丙酸倍氯米松治疗和胃肠道移植物抗宿主病的预后血浆生物标志物","authors":"Yoshihiro Inamoto, Ayumu Ito, Toshihisa Nakashima, Asako Usui, Wataru Takeda, Takashi Tanaka, Sung-Won Kim, Shigehisa Kitano, Keisuke Watanabe, Kana Kusaba, Yu Aruga, Chiaki Ikeda, Minoru Kojima, Naoki Maezawa, Hirotaka Matsui, Hironobu Hashimoto, Chitose Ogawa, Takahiro Fukuda","doi":"10.1007/s12185-025-03973-7","DOIUrl":null,"url":null,"abstract":"<p><p>The real-world outcomes of oral beclomethasone dipropionate (BDP) for gastrointestinal graft-versus-host disease (GVHD) were evaluated in a single-center, prospective, observational study of 167 patients who developed histologically confirmed gastrointestinal GVHD. The median patient age was 55 years (range 10-71). The initial GVHD grade was mostly IIa (n = 138). BDP was used without systemic corticosteroids in 73 patients (44%), resulting in a decreased proportion of patients who received systemic corticosteroid administration from 76 to 58% (P = 0.001). The 4-week gastrointestinal response rate after BDP therapy, the primary endpoint, was 73% (95% CI 66-80%) compared with 68% (95% CI 55-78%) before BDP implementation. The proportion of patients with maximum gastrointestinal stage ≥ 2 was lower after than before BDP implementation (18% versus 35%, respectively, P = 0.004). The 1 year cumulative incidence of nonrelapse mortality (NRM) after gastrointestinal GVHD therapy was 15% after and 22% before BDP implementation (P = 0.12). The 4-week gastrointestinal response rate was lower in patients with elevated ST2 or REG3α levels than the remaining patients (36% versus 73%, P = 0.03). The 1 year NRM was higher in patients with elevated ST2 or ANG2 levels than the remaining patients (64% versus 12%, P < 0.001). This study characterized the outcomes of BDP therapy in real-world patients.</p>","PeriodicalId":13992,"journal":{"name":"International Journal of Hematology","volume":" ","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2025-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Oral beclomethasone dipropionate therapy and prognostic plasma biomarkers for gastrointestinal graft-versus-host disease.\",\"authors\":\"Yoshihiro Inamoto, Ayumu Ito, Toshihisa Nakashima, Asako Usui, Wataru Takeda, Takashi Tanaka, Sung-Won Kim, Shigehisa Kitano, Keisuke Watanabe, Kana Kusaba, Yu Aruga, Chiaki Ikeda, Minoru Kojima, Naoki Maezawa, Hirotaka Matsui, Hironobu Hashimoto, Chitose Ogawa, Takahiro Fukuda\",\"doi\":\"10.1007/s12185-025-03973-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The real-world outcomes of oral beclomethasone dipropionate (BDP) for gastrointestinal graft-versus-host disease (GVHD) were evaluated in a single-center, prospective, observational study of 167 patients who developed histologically confirmed gastrointestinal GVHD. The median patient age was 55 years (range 10-71). The initial GVHD grade was mostly IIa (n = 138). BDP was used without systemic corticosteroids in 73 patients (44%), resulting in a decreased proportion of patients who received systemic corticosteroid administration from 76 to 58% (P = 0.001). The 4-week gastrointestinal response rate after BDP therapy, the primary endpoint, was 73% (95% CI 66-80%) compared with 68% (95% CI 55-78%) before BDP implementation. The proportion of patients with maximum gastrointestinal stage ≥ 2 was lower after than before BDP implementation (18% versus 35%, respectively, P = 0.004). The 1 year cumulative incidence of nonrelapse mortality (NRM) after gastrointestinal GVHD therapy was 15% after and 22% before BDP implementation (P = 0.12). The 4-week gastrointestinal response rate was lower in patients with elevated ST2 or REG3α levels than the remaining patients (36% versus 73%, P = 0.03). The 1 year NRM was higher in patients with elevated ST2 or ANG2 levels than the remaining patients (64% versus 12%, P < 0.001). 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引用次数: 0
摘要
口服二丙酸倍氯米松(BDP)治疗胃肠道移植物抗宿主病(GVHD)的实际结果在一项单中心、前瞻性、观察性研究中进行了评估,该研究纳入了167例组织学证实的胃肠道移植物抗宿主病患者。患者年龄中位数为55岁(范围10-71岁)。初始GVHD分级多数为IIa级(n = 138)。73例患者(44%)在不使用全身皮质类固醇的情况下使用BDP,导致接受全身皮质类固醇治疗的患者比例从76%下降到58% (P = 0.001)。BDP治疗后的4周胃肠道反应率(主要终点)为73% (95% CI 66-80%),而BDP实施前为68% (95% CI 55-78%)。实施BDP后最大胃肠道分期≥2期的患者比例低于实施前(分别为18%和35%,P = 0.004)。胃肠道GVHD治疗后的1年累计非复发死亡率(NRM)在实施BDP后为15%,在实施BDP前为22% (P = 0.12)。ST2或REG3α水平升高的患者4周胃肠道反应率低于其余患者(36%对73%,P = 0.03)。ST2或ANG2水平升高的患者的1年NRM高于其他患者(64% vs 12%, P
Oral beclomethasone dipropionate therapy and prognostic plasma biomarkers for gastrointestinal graft-versus-host disease.
The real-world outcomes of oral beclomethasone dipropionate (BDP) for gastrointestinal graft-versus-host disease (GVHD) were evaluated in a single-center, prospective, observational study of 167 patients who developed histologically confirmed gastrointestinal GVHD. The median patient age was 55 years (range 10-71). The initial GVHD grade was mostly IIa (n = 138). BDP was used without systemic corticosteroids in 73 patients (44%), resulting in a decreased proportion of patients who received systemic corticosteroid administration from 76 to 58% (P = 0.001). The 4-week gastrointestinal response rate after BDP therapy, the primary endpoint, was 73% (95% CI 66-80%) compared with 68% (95% CI 55-78%) before BDP implementation. The proportion of patients with maximum gastrointestinal stage ≥ 2 was lower after than before BDP implementation (18% versus 35%, respectively, P = 0.004). The 1 year cumulative incidence of nonrelapse mortality (NRM) after gastrointestinal GVHD therapy was 15% after and 22% before BDP implementation (P = 0.12). The 4-week gastrointestinal response rate was lower in patients with elevated ST2 or REG3α levels than the remaining patients (36% versus 73%, P = 0.03). The 1 year NRM was higher in patients with elevated ST2 or ANG2 levels than the remaining patients (64% versus 12%, P < 0.001). This study characterized the outcomes of BDP therapy in real-world patients.
期刊介绍:
The International Journal of Hematology, the official journal of the Japanese Society of Hematology, has a long history of publishing leading research in hematology. The journal comprises articles that contribute to progress in research not only in basic hematology but also in clinical hematology, aiming to cover all aspects of this field, namely, erythrocytes, leukocytes and hematopoiesis, hemostasis, thrombosis and vascular biology, hematological malignancies, transplantation, and cell therapy. The expanded [Progress in Hematology] section integrates such relevant fields as the cell biology of stem cells and cancer cells, and clinical research in inflammation, cancer, and thrombosis. Reports on results of clinical trials are also included, thus contributing to the aim of fostering communication among researchers in the growing field of modern hematology. The journal provides the best of up-to-date information on modern hematology, presenting readers with high-impact, original work focusing on pivotal issues.