Myelodysplastic Syndromes
Questions discussed in this category
Is there a role for increasing the dose if not yet maximum? (Hb ~8)
Bone marrow biopsy does not meet criteria for MDS and no other identifiable cause of the cytopenias.
How would you sequence these therapies given approval for both?
Do next generation sequencing results influence diagnostic and therapeutic decisions for patients with MDS?
What do you think about the long term risk of AML with romiplostim with longer follow up studies? What about using other TPO agonists like eltrombopag...
If yes, how does that affect management?
If no, what are your indications for BM biopsy?
Per the new data from the COMMANDS trial, Platzbecker et al., PMID 37311468
Would a negative NGS eliminate the possibility of MDS?
Is bone marrow biopsy indicated in a patient with pancytopenia with a negative NGS panel?
E.g. TET2 mutation at < 10% allele frequency
Patient on JAK2i, ESA, transfusion dependent
Would you use a trial of dexamethasone for a patient with thrombocytopenia?
If so, how do you incorporate GCSF into treatment of these patients?
E.g. would you dose-reduce or continue at same dose?
Baseline ANC was in the normal range
i.e. similar to CKD anemia?
Will you be using the IPSS-M in place of the IPSS-R? How will you be using IPSS-M in practice?
For instance, if clonal hematopoiesis of indeterminate potential (CHIP) suspected
In the case of subtle single lineage dysplasia with normal cytogenetics, do you routinely perform NGS testing for CHIP-type clonal mutations?
Do you ...
Would this change with someone who has a history of thrombosis (e.g. DVT/PE, MI, CVA)?
Would this change with someone who is more fit vs more frail?
Are there particular mutations (eg SF3B1) or syndromes (eg MDS/MPN overlaps such as MDS/MPN-RS-T) where you are more apt to using lenalidomide?
Can results from emerging AML data be extrapolated to high risk MDS populations?
Is there data to guide the choice of continuing the HMA in combinati...
Given the rarity of this in MF, is it still predictive of response to lenalidomide therapy?
Do we continue the hypomethylating agent indefinitely?
Is there a preferred low dose splenic irradiation regimine?
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Papers discussed in this category
The Lancet. Oncology, 2009-03
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2002-05-15
Cancer, 2011-06-15
American journal of hematology, 2009-09
Cancer, 2010-08-15
The New England journal of medicine, 2016-11-24
The Lancet. Haematology, 2018-01
Blood Adv,
Blood, 2015-11-19
Blood, 2017 Apr 19
Blood, 2021 Jul 13
Therapeutic advances in hematology, 2012-04
J Clin Oncol, 2021 Jan 13
American journal of hematology, 2019-04
Leukemia, 2023 May 05
Blood, 2018 Dec 13
The New England journal of medicine, 2020 Jan 09
Lancet (London, England), 2023 Jun 10
Blood advances, 2023 Jul 25
N Engl J Med,
Am J Hematol, 2019 Aug 07
Blood, 2017-09-28
Haematologica, 2009-01
Blood, 2020 Jul 09
Leukemia, 2022 Dec 03
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2019-01-01
Nat Genet, 2020 Nov
Cancer, 2014-06-15
The Lancet. Haematology, 2018-03
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2023 Jun 09
Lancet (London, England), 2023 Dec 01
Journal of the American Medical Association, 1953 Jul 11
Blood advances, 2023 Jul 25
Nature genetics, 2023 Aug 24
NEJM evidence, 2022 Jun 12
Haematologica, 2024 Oct 24
Journal of clinical medicine, 2021 Dec 22