Suppr超能文献

艾曲泊帕对儿童再生障碍性贫血免疫抑制治疗的辅助作用。

Adjunctive effects of eltrombopag on immunosuppressive therapy for childhood aplastic anemia.

作者信息

Eguchi Katsuhide, Ishimura Masataka, Ohga Shouichi, Endo Saori, Saito Shoji, Kamimura Sachiyo, Keino Dai, Kato Shota, Azuma Yoshihiro, Watanabe Atsushi, Inoue Akiko, Higa Takeshi, Ozono Shuichi, Fujita Naoto, Watanabe Kenichiro, Takahashi Yoshiyuki

机构信息

Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Department of Pediatrics, Gifu University Graduate School of Medicine, Gifu, Japan.

出版信息

Int J Hematol. 2025 Apr;121(4):533-542. doi: 10.1007/s12185-024-03903-z. Epub 2024 Dec 27.

Abstract

Eltrombopag is used with first-line immunosuppressive therapy for adult aplastic anemia, although its practical utility in childhood remains unclear. We retrospectively analyzed the outcomes of pediatric patients who received eltrombopag in Japan. Of the 27 eligible patients, 23 (85%) were previously treated, and 15 (56%) had severe or very-severe disease. Seventeen (63%) received eltrombopag with or after rabbit anti-thymocyte globulin plus cyclosporin-A. Within the first year of eltrombopag therapy, 12 patients showed a good or partial response, 15 showed no response, and 8 non-responders successfully underwent hematopoietic cell transplantation. Within the first 3 months after eltrombopag therapy, all but one of the transfusion-dependent responders became transfusion-independent. At 12 months, 6 of 12 responders were disease-free off-treatment. The one-year overall response rate was higher for severe or very-severe than non-severe cases (p = 0.006). Multivariable analysis showed that very-severe disease at the start of eltrombopag therapy was a predictor of being disease-free off-treatment (p = 0.03). No cytogenetic abnormalities developed, but myelofibrosis occurred 4 months after eltrombopag therapy in one non-responder with very-severe disease. The first 3 months' response to adjunctive eltrombopag may guide to the safe and effective use for the cure of disease, although prospective trials are needed to determine its long-term effects.

摘要

艾曲泊帕与一线免疫抑制疗法联合用于治疗成人再生障碍性贫血,但其在儿童患者中的实际效用仍不明确。我们回顾性分析了在日本接受艾曲泊帕治疗的儿科患者的治疗结果。在27例符合条件的患者中,23例(85%)曾接受过治疗,15例(56%)患有重度或极重度疾病。17例(63%)在接受兔抗胸腺细胞球蛋白加环孢素A治疗的同时或之后接受了艾曲泊帕治疗。在艾曲泊帕治疗的第一年内,12例患者显示出良好或部分缓解,15例无反应,8例无反应者成功接受了造血细胞移植。在艾曲泊帕治疗后的前3个月内,除1例输血依赖型缓解者外,其他患者均不再依赖输血。在12个月时,12例缓解者中有6例在停止治疗后无疾病迹象。重度或极重度病例的一年总缓解率高于非重度病例(p = 0.006)。多变量分析显示,在开始使用艾曲泊帕治疗时患有极重度疾病是停止治疗后无疾病迹象的一个预测因素(p = 0.03)。未出现细胞遗传学异常,但1例患有极重度疾病的无反应者在接受艾曲泊帕治疗4个月后发生了骨髓纤维化。尽管需要进行前瞻性试验来确定其长期效果,但艾曲泊帕辅助治疗开始3个月的反应可能有助于指导其安全有效地用于疾病的治愈。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验