Treatment of Advanced Systemic Mastocytosis with Midostaurin: Practical Guidance for Optimal Therapy and Management
- PMID: 36425146
- PMCID: PMC9652003
- DOI: 10.4084/MJHID.2022.073
Treatment of Advanced Systemic Mastocytosis with Midostaurin: Practical Guidance for Optimal Therapy and Management
Abstract
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.
Keywords: Guidance; Management; Midostaurin; Systemic mastocytosis.
Conflict of interest statement
Competing interests: The authors declare no conflict of Interest. Conflicts of Interest. CP reports to have participated in Advisory Boards for Novartis and AbbVie, outside the submitted work. LF has nothing to disclose. VF reports to have participated in an Advisory Board for Amgen, outside the submitted work. FIG has nothing to disclose. NP has nothing to disclose. PP reports payment or honoraria as a speaker and for Advisory Boards from Novartis Italia, outside the submitted work. AR reports consulting fees from Novartis and to have participated on a Data Safety Monitoring Board/Advisory Board for Novartis, outside the submitted work.
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