Educational content on VJHemOnc is intended for healthcare professionals only. By visiting this website and accessing this information you confirm that you are a healthcare professional.

Share this video  

EBMT 2023 | The impact of early ruxolitinib treatment on OS in the COMFORT-I and COMFORT-II studies

Jean-Jacques Kiladjian, MD, PhD, Saint-Louis Hospital & Paris Diderot University, Paris, France, highlights the results from the pooled analysis of the COMFORT-I (NCT00952289) and COMFORT-II (NCT00934544) studies. Prof. Kiladjian explains that the study showed significantly improved overall survival (OS) for patients with myelofibrosis (MF) who initiated ruxolitinib treatment early compared to patients who started treatment later. This interview took place at the 49th Annual Meeting of the European Group for Blood and Marrow Transplantation (EBMT) held in Paris, France.

These works are owned by Magdalen Medical Publishing (MMP) and are protected by copyright laws and treaties around the world. All rights are reserved.

Transcript (edited for clarity)

We recently made a post-hoc analysis of the patients enrolled in the two COMFORT studies. COMFORT-I and COMFORT-II to see whether starting treatment early improves the outcome. We analyze the patients according to their diagnosis before starting treatment, before 12 months, shorter than 12 months, or after 12 months, one year after the diagnosis. Indeed, we could demonstrate that overall survival was significantly improved among patients who initiated ruxolitinib earlier, around 63% compared to around 50% in patients who started later...

We recently made a post-hoc analysis of the patients enrolled in the two COMFORT studies. COMFORT-I and COMFORT-II to see whether starting treatment early improves the outcome. We analyze the patients according to their diagnosis before starting treatment, before 12 months, shorter than 12 months, or after 12 months, one year after the diagnosis. Indeed, we could demonstrate that overall survival was significantly improved among patients who initiated ruxolitinib earlier, around 63% compared to around 50% in patients who started later. So, a better survival if you start treatment soon. It makes sense because patients have less disease burden, often the JAK2 mutation is less elevated, and they have less symptoms. Starting early the treatment, when necessary, of course, is probably associated with a better outcome. So, we don’t need to wait too long because patients may progress if you don’t treat them too late, and then starting early the treatment, may improve the outcome.

Read more...

Disclosures

Advisory boards for Novartis, Abbvie, BMS, AOP Orphan.