Stanford University School of Medicine, Stanford, CA;
Blood. 2013 Mar 28;121(13):2393-401. doi: 10.1182/blood-2012-09-458521. Epub 2013 Jan 16.
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.
系统性肥大细胞增多症(SM)的特征是肿瘤性肥大细胞的积累,并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 2 个疾病部位均表现出晚期特征。这些变体,出于本报告的目的,此后统称为晚期 SM,通常表现为器官损伤和生存期缩短。与通常通过非细胞毒性抗介质治疗来控制症状的惰性 SM 不同,晚期 SM 通常需要细胞减少来控制疾病。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延长生存时间。先前定义的反应标准已针对晚期 SM 的异质表现和现有药物的有限作用进行了调整。然而,对 SM 的分子发病机制的理解以及相应的靶向治疗前景的最新进展使其成为修改这些标准的优先事项。我们目前的研究是一个国际专家组的成果,总结了完成这项任务的挑战,并提出了一个新的反应标准建议,该建议建立在前瞻性建议的基础上,应有助于临床试验中的反应评估。