Truly grateful and proud to be part of a defining moment at #ASH2025.
Contributing as an author to the EPCORE FL-1 trial — with simultaneous publication in @TheLancet and global regulatory impact — was a very special milestone in my academic journey. 🧵👇
Our new review on AI in lymphoma diagnosis is out.
A realistic look at how AI can support — not replace — clinical practice.
Grateful to Marianne for the invitation and collaboration.
🔗 Link: https://t.co/4ljrzYkyt0
#ASH2025 was a meaningful milestone in my academic journey.
Being an author on 4 oral presentations and 3 posters highlights the strength of collaborative clinical research and team science.
Grateful to my mentor Eduardo Rego and the IDOR research team.
One of the moments I was most proud of at #ASH2025 was seeing Luiza Lapolla present data from the Brazilian AML Registry, highlighting how social determinants shape AML outcomes using real-world national data.
@abhhoficial
Glad to contribute as an author to an oral presentation at #ASH2025 on golca ± rituxi in R/R FL.
High ORR, durable responses, and manageable toxicity, even in heavily pretreated patients, supporting the role of targeted combinations in later lines.
Grateful to contribute as an author to the TRAVERSE phase 2 study presented at #ASH2025.
A chemotherapy-free triplet regimen, AVR in treatment-naïve MCL, showed deep responses and high MRD negativity, even in biologically high-risk subgroups.
For those who want to dive deeper, the full EPCORE FL-1 data are published in The Lancet and have already led to FDA and ANVISA approval.
https://t.co/AnJYt3C6Fz
Truly grateful and proud to be part of a defining moment at #ASH2025.
Contributing as an author to the EPCORE FL-1 trial — with simultaneous publication in @TheLancet and global regulatory impact — was a very special milestone in my academic journey. 🧵👇
Taken together, EPCORE FL-1 shows that epcoritamab + R² achieves deep and durable responses, delays the need for subsequent therapy, and maintains a predictable, manageable safety profile, supporting its role as a new standard of care.
🇧🇷 Proud to represent Brazil in this milestone and to be part of a global study with strong participation from Brazilian centers, contributing to a change in standard of care.
Why this matters:
✔️First bispecific antibody approved in combination for FL
✔️Fixed-duration, chemotherapy-free regimen
✔️Immediate impact on treatment sequencing and clinical practice
Safety profile was manageable and predictable, with no new safety signals:
• CRS mostly grade 1–2; no grade ≥3 CRS
• No tx discontinuations due to CRS
• Neutropenia and infections were manageable
• >90% relative dose intensity maintained
Compatible with outpatient delivery.
Despite still maturing follow-up, EPCORE FL-1 shows a statistically significant early OS signal, with separation of the curves and an HR of 0.38, favoring epcoritamab + R².
Key efficacy results:
• ORR: 95.7% vs 81.0%
• CR: 83% vs 50%
• 79% reduction in risk of progression or death (HR 0.21)
Benefit consistent across prespecified subgroups.
Follicular lymphoma remains a chronic disease for most patients, with diminishing benefit after each line of therapy.
EPCORE FL-1 addressed a critical unmet need: a fixed-duration, chemo-free strategy capable of delivering deep and durable remissions.
📢We are proud to announce that the EHA-EMN guidelines for the diagnosis, treatment and follow-up of #MultipleMyeloma are now available online!
Huge thanks to Evangelos Terpos for coordinating such outstanding work! 👉https://t.co/0tLcVmnpa4 @thanosdimop@EHA_Hematology