Clofarabine monotherapy in refractory multisystem LCH with gastrointestinal involvement.

IF 1.2 4区 医学 Q4 HEMATOLOGY
Stephanie Aronson, Vivian Tang, Klaudia Cios, Meredith Pittman, Mahmut Y Çeliker
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引用次数: 0

Abstract

Langerhans Cell Histiocytosis (LCH) is a rare histiocytic disorder that involves various organ systems. Recognizing gastrointestinal (GI) tract involvement in LCH is crucial, as GI cases, even without high-risk organ involvement, may be refractory to initial as well as second line therapy. Here, we report two cases of LCH with GI involvement, that were refractory to vinblastine, prednisone and cytarabine, and ultimately required clofarabine to reach clinical remission. We propose that clofarabine should be further studied as a first choice for second line treatment for GI-LCH cases and that GI involvement should be considered as high risk in the LCH risk stratification algorithm.

氯法拉滨单药治疗难治性多系统LCH伴胃肠道受累。
朗格汉斯细胞组织细胞增多症(LCH)是一种罕见的组织细胞疾病,涉及多个器官系统。识别LCH的胃肠道受累是至关重要的,因为胃肠道病例,即使没有高危器官受累,也可能难以接受初始和二线治疗。在这里,我们报告了两例LCH伴胃肠道受累的病例,这些病例对长春花碱、强的松和阿糖胞苷难治性,最终需要氯法拉滨才能达到临床缓解。我们建议进一步研究氯法拉滨作为GI-LCH病例二线治疗的首选,并且在LCH风险分层算法中应将GI累及视为高风险。
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来源期刊
CiteScore
2.60
自引率
5.90%
发文量
71
审稿时长
6-12 weeks
期刊介绍: PHO: Pediatric Hematology and Oncology covers all aspects of research and patient management within the area of blood disorders and malignant diseases of childhood. Our goal is to make PHO: Pediatric Hematology and Oncology the premier journal for the international community of clinicians and scientists who together aim to define optimal therapeutic strategies for children and young adults with cancer and blood disorders. The journal supports articles that address research in diverse clinical settings, exceptional case studies/series that add novel insights into pathogenesis and/or clinical care, and reviews highlighting discoveries and challenges emerging from consortia and conferences. Clinical studies as well as basic and translational research reports regarding cancer pathogenesis, genetics, molecular diagnostics, pharmacology, stem cells, molecular targeting, cellular and immune therapies and transplantation are of interest. Papers with a focus on supportive care, late effects and on related ethical, legal, psychological, social, cultural, or historical aspects of these fields are also appreciated. Reviews on important developments in the field are welcome. Articles from scientists and clinicians across the international community of Pediatric Hematology and Oncology are considered for publication. The journal is not dependent on or connected with any organization or society. All submissions undergo rigorous peer review prior to publication. Our Editorial Board includes experts in Pediatric Hematology and Oncology representing a wide range of academic and geographic diversity.
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