Myelodysplastic Syndrome (MDS)
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- Опубліковано 8 сер 2020
- Myelodysplastic syndrome (MDS) is a heterogenous blood disease affecting WBCs, RBCs, and/or platelets. Although it is considered as a not-curable blood cancer, many patients can be treated with newly developed targeted therapy.
Thanks 🙏
Thanks! very good explanation of the different types of MDS 👍
Thank you prof. i learnt much from this video and i appreciate it. from Cambodia.
The new 5th edition of WHO classification was published recently.
It changed the name of MDS to Myelodysplastic neoplasm.
The dysplasia should be more than 10% for Dx.
Also there are some changes in classification:
For example, no clear distinction between single and multiple lineage dysplasia. Hypoplastic MDS is now a distinct type of MDS.
www.nature.com/articles/s41375-022-01613-1#Tab8
At the same time, ICC (International Consensus Classification) published another classification which is somewhat different from WHo classification. For example, MDS excess blasts 2 (now MDS-IB2) was reclassified as MDS/AML. So, MDS-EB2 now can be considered as AML for treatment.
I believe the participant pathologists of both WHo and ICC should meet and draw a real universal classification.
COMMANDS 3 trial where Luspatercept was compared with ESA (eg, Epogen, Procrit, Retacrit) for low or intermediate risk MDS showed luspatercept was better than ESA in efficacy (transfusion independency rate). However, most patients (>70%) were MDS-ring siderobladts, adverse effects were more prevalent in the luspatercept group, the mortality rates were not different between luspatercept and ESA groups.
www.mdedge.com/hematology-oncology/article/263215/myelodysplastic-syndrome/paradigm-shift-luspatercept-mds?channel=39313
In August 2023,
The FDA has approved luspatercept-aamt (Reblozyl) for the treatment of anemia without prior erythropoiesis-stimulating agent (ESA) use in adult patients with very low- to intermediate-risk myelodysplastic syndrome (MDS) who may require regular red blood cell (RBC) transfusions.1
The regulatory decision is supported by interim findings from the phase 3 COMMANDS trial (please read my comment below) in which luspatercept had superior efficacy of concurrent RBC transfusion independence (RBC-TI) and hemoglobin (Hb) increase vs epoetin alfa, irrespective of ring sideroblast status.
Error correction:
At 4:00 myeloblast should be myelocyte.
Thank you Doctor
Error:
At 4:00, Maturation arrest at myelocyte level not myeloblast.
Imetelstat:
New drug for EPO refractory MDS was approved by FDA.
www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-imetelstat-low-intermediate-1-risk-myelodysplastic-syndromes-transfusion-dependent
안녕하세요. 캐나다에서 살고 있습니다. 오빠가 골수형성이상 증후군 진단을 받아서 제가 골수이식을 해줄 수 있는지 검사를 해보려고 합니다. 한국에 갈 상황이 아닌데 밴쿠버 병원 의료 기술을 믿을 수 있을지 걱정이 됩니다 의사분들께 감사하지만.. 어려운 수술이될지 궁금해서 알아보고 있는데요.. 조언 좀 들을 수 있을지요??
올려놓은 유투브강의를 서너번 들으시면 어떤에 경우 동종조혈모세포이식이 필요한지 어떤 때는 필요없는지 이해하실 겁니다.
이식하는 병원에서 이식전문가가 하므로 어디서 하던지 차이가 없을겁니다
Did we almost find the cure of this disease?