Papayannidis Cristina, Federico Vincenzo, Fianchi Luana, Pregno Patrizia, Pugliese Novella, Romano Alessandra, Grifoni Federica Irene
RCCS, Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seragnoli", Bologna Italy.
Haematology and Stem Cell Transplant Unit, Presidio Ospedaliero "Vito Fazzi", Lecce, Italy.
Mediterr J Hematol Infect Dis. 2022 Nov 1;14(1):e2022073. doi: 10.4084/MJHID.2022.073. eCollection 2022.
Systemic mastocytosis (SM) is a rare disease with a range of clinical presentations, and the vast majority of patients have a KIT D816V mutation that results in a gain of function. The multikinase/KIT inhibitor midostaurin inhibits the D816V mutant and has a well-established role in treating advanced SM. Even if considered the standard of therapy, some open questions remain on optimizing midostaurin management in daily practice. The current review presents the opinions of a group of experts who met to discuss routine practice using midostaurin in patients with advanced SM. The efficacy and safety of midostaurin in Phase 2 trials are overviewed, followed by practical guidance for optimal therapy management and adverse events during therapy with midostaurin. Specific guidance is given for initiating therapy and evaluating response with midostaurin as general assessment and laboratory, instrumental, pathological, and molecular exams. Special consideration is given to dose interruption, reduction, and discontinuation of therapy, as well as adverse event management and supportive therapy. Patients should be informed about possible side effects and receive practical advice to avoid or limit them and antiemetic prophylaxis so that therapy with midostaurin can continue as long as clinical benefit is observed or until unacceptable toxicity occurs. Lastly, considerations on the use of midostaurin during the ongoing Covid-19 pandemic are made. The overall scope is to provide guidance that can be useful in daily practice for clinicians using midostaurin to treat patients with advanced SM.
系统性肥大细胞增多症(SM)是一种临床表现多样的罕见疾病,绝大多数患者存在KIT D816V突变,该突变导致功能获得。多激酶/KIT抑制剂米哚妥林可抑制D816V突变体,在治疗晚期SM方面具有公认的作用。即使被视为治疗标准,但在日常实践中优化米哚妥林的管理仍存在一些未解决的问题。本综述介绍了一组专家的意见,他们会面讨论了在晚期SM患者中使用米哚妥林的常规做法。概述了米哚妥林在2期试验中的疗效和安全性,随后给出了米哚妥林治疗期间最佳治疗管理和不良事件的实用指南。针对开始治疗以及使用米哚妥林评估反应给出了具体指南,包括一般评估以及实验室、仪器、病理和分子检查。特别考虑了治疗的剂量中断、减少和停药,以及不良事件管理和支持性治疗。应告知患者可能的副作用,并给予避免或限制副作用以及预防呕吐的实用建议,以便只要观察到临床获益或直至出现不可接受的毒性,米哚妥林治疗就能持续进行。最后,对在当前新冠疫情期间使用米哚妥林的情况进行了考量。总体目的是为临床医生在日常实践中使用米哚妥林治疗晚期SM患者提供有用的指导。