Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis driven by mutations of MAPK pathway genes (e.g., BRAF, MAP2K1). Its clinical spectrum ranges from organlimited to diffuse, life-threatening forms. The prognosis of ECD was considered to be poor, but recent targeted treatments (i.e., MAPK inhibitors, such as BRAF-inhibitors, BRAFi, and MEK-inhibitors, MEKi) greatly improved patients’ outcomes. Effective strategies to mitigate toxicity while maintaining disease control are needed. We provide preliminary evidence that a treatment holiday protocol can reduce vemurafenib-associated toxicity and overall drug exposure.
Treatment holidays in patients with Erdheim-Chester disease receiving vemurafenib: a prospective pilot study / Pegoraro, Francesco; Catamerò, Francesco; Peyronel, Francesco; Allegretta, Federica; Palazzini, Giulia; Diamond, Eli L; Vaglio, Augusto. - In: BLOOD ADVANCES. - ISSN 2473-9529. - ELETTRONICO. - (2025), pp. 0-0. [10.1182/bloodadvances.2024015399]
Treatment holidays in patients with Erdheim-Chester disease receiving vemurafenib: a prospective pilot study
Pegoraro, Francesco;Catamerò, Francesco;Peyronel, Francesco;Allegretta, Federica;Palazzini, Giulia;Vaglio, Augusto
2025
Abstract
Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis driven by mutations of MAPK pathway genes (e.g., BRAF, MAP2K1). Its clinical spectrum ranges from organlimited to diffuse, life-threatening forms. The prognosis of ECD was considered to be poor, but recent targeted treatments (i.e., MAPK inhibitors, such as BRAF-inhibitors, BRAFi, and MEK-inhibitors, MEKi) greatly improved patients’ outcomes. Effective strategies to mitigate toxicity while maintaining disease control are needed. We provide preliminary evidence that a treatment holiday protocol can reduce vemurafenib-associated toxicity and overall drug exposure.I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.