首页> 外文期刊>Blood: The Journal of the American Society of Hematology >International Working Group-Myeloproliferative Neoplasms Research and Treatment (IWG-MRT) & European Competence Network on Mastocytosis (ECNM) consensus response criteria in advanced systemic mastocytosis.
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International Working Group-Myeloproliferative Neoplasms Research and Treatment (IWG-MRT) & European Competence Network on Mastocytosis (ECNM) consensus response criteria in advanced systemic mastocytosis.

机译:国际工作组-骨髓增生性肿瘤研究和治疗(IWG-MRT)和欧洲细胞吞噬作用能力网络(ECNM)对晚期系统性细胞吞噬作用的共识反应标准。

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摘要

Systemic mastocytosis (SM) is characterized by accumulation of neoplastic mast cells and is classified into indolent and aggressive forms. The latter include aggressive SM (ASM), mast cell leukemia (MCL), and SM associated with a myeloid neoplasm wherein 1 or both disease compartments exhibit advanced features. These variants, henceforth collectively referred to as advanced SM for the purposes of this report, are typically characterized by organ damage and shortened survival duration. In contrast to indolent SM, in which symptoms are usually managed by noncytotoxic antimediator therapy, cytoreduction is usually necessary for disease control in advanced SM. Unfortunately, current drug treatment of these patients rarely results in complete clinical and histopathologic remissions or improved survival time. Previously defined response criteria were adapted to the heterogeneous presentations of advanced SM and the limited effects of available drugs. However, recent advances in understanding the molecular pathogenesis of SM and the corresponding prospect in targeted therapy make it a priority to modify these criteria. Our current study is the product of an international group of experts and summarizes the challenges in accomplishing this task and forwards a new proposal for response criteria, which builds on prior proposals and should facilitate response evaluation in clinical trials.
机译:全身性肥大细胞增多症(SM)的特征是肿瘤性肥大细胞蓄积,分为惰性和侵袭性形式。后者包括侵袭性SM(ASM),肥大细胞白血病(MCL)和与髓系肿瘤相关的SM,其中1个或两个疾病区室均显示晚期特征。在本报告中,这些变体以下统称为高级SM,通常以器官损伤和生存期缩短为特征。与惰性SM相比,症状通常通过无细胞毒性的抗介体疗法来控制,而晚期SM的疾病控制通常需要细胞减少。不幸的是,目前对这些患者的药物治疗很少导致完全的临床和组织病理学缓解或改善的生存时间。先前定义的反应标准适用于晚期SM的异质表现和可用药物的有限作用。但是,在了解SM的分子发病机理方面的最新进展以及靶向治疗的相应前景使修改这些标准成为优先事项。我们当前的研究是一个国际专家小组的成果,它总结了完成此任务所面临的挑战,并提出了新的反应标准建议,该建议以先前的建议为基础,应有助于临床试验中的反应评估。

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