DelveInsight’s “Myelodysplastic Syndrome Market Insight, Epidemiology, and Market Forecast – 2034” report delivers an in-depth understanding of the Myelodysplastic Syndrome historical and forecasted epidemiology as well as the Myelodysplastic Syndrome market trends in the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan.
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Key Takeaways from the Myelodysplastic Syndrome Market Report
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Myelodysplastic Syndrome Epidemiology Segmentation in the 7MM
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Myelodysplastic Syndrome Marketed Drugs
VIDAZA is a pyrimidine nucleoside analog of cytidine. VIDAZA is believed to exert its antineoplastic effects by causing hypomethylation of DNA and direct cytotoxicity on abnormal hematopoietic cells in the bone marrow. The concentration of azacitidine required for maximum inhibition of DNA methylation in vitro does not cause major suppression of DNA synthesis. It was first approved by the US FDA in May 2004 for the Myelodysplastic Syndrome treatment.
DACOGEN is a nucleoside metabolic inhibitor indicated for the treatment of adult patients with myelodysplastic syndromes including previously treated and untreated, de novo and secondary MDS. Decitabine-induced hypomethylation in neoplastic cells may restore normal function to genes that are critical for the control of cellular differentiation and proliferation. In rapidly dividing cells, the cytotoxicity of decitabine may also be attributed to the formation of covalent adducts between DNA methyltransferase and decitabine incorporated into DNA. Non-proliferating cells are relatively insensitive to decitabine. It was first approved by the US FDA in May 2006.
Myelodysplastic Syndrome Emerging Drugs
Venetoclax by Abbvie is a first-in-class targeted medicine designed to selectively bind and inhibit the B-cell lymphoma-2 (BCL-2) protein. Currently, the drug is being investigated in a Phase III trial to treat adult patients with newly diagnosed higher-risk Myelodysplastic Syndrome. Moreover, in July 2021, the combination was granted Breakthrough Therapy Designation in higher risk Myelodysplastic Syndrome.
Tamibarotene is an oral selective retinoic acid receptor alpha (RARA) agonist being developed for genomically defined subsets of patients whose disease is characterized by the overexpression of the RARA gene. Approximately 50% of Myelodysplastic Syndrome patients and 30% of AML patients have RARA overexpression. When RARA is expressed more than its tightly controlled natural ligand, cells in the bone marrow may not differentiate into healthy myeloid cells, which can lead to hematological malignancies. However, when oral tamibarotene is administered, tamibarotene binds to RARα, allowing for the restoration of gene expression and myeloid differentiation. It is currently being investigated in the Phase III SELECT-MDS-1 trial in newly diagnosed higher-risk myelodysplastic syndrome patients with RARA overexpression.
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Myelodysplastic Syndrome Drugs Market Insights
There is a vast pipeline of targeted agents under pre-clinical and clinical development, potentially able to modify the natural history of the diverse disease spectrum of MDS. The B-cell leukemia/lymphoma-2 (BCL-2) inhibitor, venetoclax is to date one of the most potent anti-apoptotic inhibitors, representing a novel promising agent. This small molecule blocks the binding of BH3 proteins to BCL-2, allowing the activation of BCL2 Antagonist/Killer/BCL2 associated X on the surface of mitochondria leading to cell death of cancer cells because of the release of cytochrome C through a mitochondrial outer membrane permeabilization (MOMP) process. IDH1 and IDH2 inhibitors have also recently shown an acceptable ORR in different clinical trials. FLT3 inhibitors represent another important potential group of targeted compounds in MDS patients harboring FLT3 mutations.
Myelodysplastic Syndrome Market Outlook
While for more than a decade the therapeutic scenario of Myelodysplastic Syndrome syndromes has been dominated by very few available regimens associated with dismal results, especially for patients with higher-risk disease and who failed HMAs, in the last 2 years there was a flow of an incredible variety of new targeted agents and investigational approaches that possibly will reach the clinical setting in short time. If currently available therapies still include HMAs, lenalidomide, growth factor support, chemotherapy, and allo-HSCT, there is now the possibility to choose among new investigational treatments rationally designed to exert targeted actions and increase the response rates in categories of patients that so far remained precision drug-orphans.
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Scope of the Myelodysplastic Syndrome Market Report
Table of Content
1 Key Insights
2 Report Introduction
3 Executive Summary of Myelodysplastic Syndrome (MDS)
4 Myelodysplastic Syndrome (MDS) Market Overview at a Glance
5 Key Events
6 Epidemiology and Market Forecast Methodology
7 Disease Background and Overview
8 Diagnostic Algorithm
9 British Society for Hematology guidelines for the Diagnosis and Evaluation of Prognosis of Adult MDS
10 Treatment
11 National Comprehensive Cancer Network recommendations for myelodysplastic syndrome
12 Myelodysplastic Syndromes: ESMO Clinical Practice Guidelines for Diagnosis, Treatment, and Follow-up
13 JSH Practical Guidelines for MDS
14 British Society for Hematology Guidelines for the Management of Adult Myelodysplastic Syndromes
15 Treatment Algorithm
16 Epidemiology and Patient Population
17 Organizations contributing toward Myelodysplastic Syndrome
18 Patient Journey
19 Marketed Drugs
20 Emerging Therapies
21 Myelodysplastic Syndrome: Seven Major Market Analysis
22 Unmet Need
23 SWOT Analysis
24 KOL Views
25 Market Access and Reimbursement
26 Appendix
27 DelveInsight Capabilities
28 Disclaimer
29 About DelveInsight
About Us
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