09/08/2026
“Can we engineer disease trajectories in MPNs?” 🎯
That question from Dr. Alessandro Lucchesi posted on LinkedIn stopped me.
For years, much of the MPN treatment conversation has focused on controlling blood counts, reducing spleen size, easing symptoms, and lowering immediate risks. Those goals remain essential. But the discussion is becoming more ambitious:
Can we intervene earlier, match the right treatment to the right patient, and actually change where the disease is headed?
This will be the central focus of RiseMPN 2026, taking place November 6–7 in Rome, Italy.
We now have more tools in the MPN arsenal. JAK inhibitors, interferons, hepcidin-axis treatments, epigenetic therapies, p53/MDM2 strategies, activin ligand traps, and other investigational approaches are expanding the possibilities.
The next challenge is determining:
• Which treatments or combinations can truly modify disease biology?
• Which patients are most likely to benefit?
• When is the best time to intervene?
• Can we delay or prevent progression rather than responding after it occurs?
Having more treatments does not automatically mean we are changing the natural history of an MPN. That still has to be proven through strong clinical research. But I am impressed that the conversation is moving beyond symptom control and asking a much bigger question: Can we deliberately change the trajectory of these diseases?
That is the direction patients have been waiting for.
Thank you to Dr. Alessandro Lucchesi for sharing this thoughtful perspective and helping move this important discussion forward. I will be watching RiseMPN 2026 closely and sharing meaningful developments with the MPN community.
Learn more: https://risempn.org
Can we engineer disease trajectories in MPNs? Rome, 6–7 November 2026.