A Sociedade Brasileira de Terapia Celular e Transplante de Medula Óssea lamenta o falecimento do Dr. Marcos Paulo Colella e presta solidariedade aos familiares, amigos e colegas, reconhecendo seu importante legado para a Hematologia brasileira.
1/ 🧵 So delighted to share our new paper, out today in Science Translational Medicine @ScienceTM. We built a CAR-T cell therapy that selectively depletes the disease-driving mutant calreticulin (mutCALR) cells in myelofibrosis — while sparing healthy blood stem cells👇
https://t.co/zfwYYSqT9h
INCREDIBLE ❤️
This will make patients with myeloma really happy ☺️
Next step, making sure everyone who needs these therapies can actually get them 🙏🏽
#ASH25@NEJM
https://t.co/Eut8C9ztNK
You can use this QR code or link
https://t.co/ftLyvtrtsO to access our recent paper on classification of myeloid neoplasms in @BCD_AACR for free for the duration of @SocietyofHemOnc next week. 🩸
#hemepath#soho2025#leusm
Excited to share our latest work @Nature! We show that the total number of hematopoietic stem cells (HSCs) in the body is restricted, challenging the classical model that HSC numbers are determined locally by the niche and introducing a new paradigm. (1/9)
https://t.co/kvFqNQ8Nxb
Congrats @r_sazevedo on her paper, out today in @BrJHaem She screened CD123 expression in AML to assess CD123 correlation w/ genotype. Timely as more anti-CD123 targeted therapies become available for AML pts #hemepath#LeuSM
https://t.co/3LllNQDlyP
Clonal hematopoiesis (CH) is common in older persons without hematologic disease - but what about those who previously had acute myeloid leukemia, and survived the disease? @ScimonkM looked at CH in 373 AML long-term survivors: https://t.co/K0dH8mNs2z (1/10)
📢 Out in @NEJMEvidence
👫N=1132 pts; age 18-60
🔹ND #AML
🔹Consolidation with IDAC vs HIDAC
🔹5-yr OS = 59% vs 58%
🔹Lower incidence of myelosuppressio & AEs with IDAC
➡️ IDAC non inferior to HIDAC
#leusm@OncoAlert
https://t.co/mtooZ8M270
@DavidSteensma Thanks for all the helpful insights Dr Steensma. Do you think we should target specific mutations (i.e.: splicing) or a common metabolic weakness (if any)? Also, do you think this result questions the AML/MDS proposed by the ICC (VIALE-A improves OS in pts with > 20% blasts)
The impact of clinical features on survival and relapse of patients diagnosed with T-cell acute lymphoblastic leukemia – a multicenter cohort study - 🇧🇷💚 https://t.co/GpX5z5ukwV
🎉Excited to present our latest work out today @Nature 1.What gives a leukemia its phenotype – the oncogenic driver or the differentiation stage of the cell-of-origin? 2.Why do RAS mutations always happen late in AML? 3.Who will relapse after VEN? https://t.co/JAHNAw33wH
ASH is redefining ANC reference ranges based on Duffy status. No patient should face uncertainty in their medical treatment because of their genetics. #ASHDEI#HealthEquity
@QMyPath@emmamgroarke@BloodAdvances@genome_gov Very nice to see our initial report reproduced in a larger cohort! Still intrigued about which is the mechanistic role of NFE2 mutations in RUNX1 FPDMM progression to AML/MDS.