Global Myelodysplastic Syndrome (MDS) Treatment Market - 2020-2027
|骨髓發育異常症候群（MDS）治療的全球市場：2020-2027 Global Myelodysplastic Syndrome (MDS) Treatment Market - 2020-2027|
|出版日期: 按訂單生產||內容資訊: 英文||
骨髓發育異常症候群（MDS），也稱為 "骨髓營養不良症" ，是一種骨髓病，可阻止骨髓產生足夠的健康血細胞。它沒有造血功能。它在老年人中更常見，在男性中比在女性中更常見。
The global myelodysplastic syndrome (MDS) treatment market size was worth US$ XX billion in 2018 and is estimated to reach US$ XX billion by 2027, growing at a CAGR of XX % during the forecast period (2020-2027).
Myelodysplastic Syndrome (MDS), also referred to as a "bone marrow failure disorder" is a type of bone marrow disorder, in which the bone marrow does not produce enough healthy blood cells. These disorders are characterized by ineffective hematopoiesis, including abnormalities in proliferation, differentiation, and apoptosis. This syndrome usually affects the geriatric population and more often in older men than women. MD syndrome is characterized by specific chromosomal mutations in Janus Kinase gene, that include deletion of q arm in one or more chromosomes and complete the deletion of chromosome 5 or 7 and an extra copy of chromosome 8. MDS is diagnosed through several techniques including blood count, peripheral blood smear test, microscopic exams, cytochemistry, flow cytometry, immunotherapy, cytogenetics, FISH, and PCR. The MDS International Foundation is a nonprofit health organization which provide psychological support as well as funding to patients for treatment of the disorder.
The global myelodysplastic syndrome (MDS) treatment market growth is driven by several factors such as the rising geriatric population, growing awareness, the emergence of novel therapeutics, government initiatives to provide target-specific treatments and favourable reimbursement policies.
Myelodysplastic syndrome is one of the most common malignant haematological diseases that occur at a rate of 4.8 cases for every 100,000 people. About 60,000 people in the U.S. live with MDS, and over 13,000 new cases are reported annually as per American Cancer Society data. The new cases diagnosed each year is increasing as the average age of the population increases. Patients may present with clinical manifestations such as anaemia, thrombocytopenia, and neutropenia.
The MDS treatment market is expected to grow significantly during the forecast period, owing to the increasing pipeline drugs, drug approvals and R&D investments in the development of novel drugs for myelodysplastic syndrome. For instance, in July 2020, the U.S. Food and Drug Administration approved Inqovi (decitabine and cedazuridine) tablets for the treatment of adult patients with myelodysplastic syndromes (MDS) and chronic myelomonocytic leukaemia (CMML). This is an important advancement in treatment options for patients with MDS, a type of blood cancer, who previously needed to visit a health care facility to receive intravenous therapy.
Also, in 2018, Lupin received approval for its Decitabine for injection, 50 mg/vial, Single-Dose Vial from the United States Food and Drug Administration (FDA) to market a generic version of Otsuka Pharmaceutical Co. Ltd's Dacogen for Injection, 50 mg/vial, single-dose vial.
However, the side effects associated with chemotherapy medications and high cost of therapeutics are expected to hamper the growth of the myelodysplastic syndrome treatment market.
Market Segment Analysis
Based on treatment type, the myelodysplastic syndrome (MDS) market is classified into chemotherapy, stem cell transplant, immune treatments, growth factors, and other treatments. Among these, the stem cell transplant (SCT) segment is expected to grow significantly over the forecast period. Stem cell transplantation offers a potentially beneficial therapy for the patients with myelodysplastic syndromes. There are two major types of SCT, one is allogeneic stem cell transplant and the other is an autologous stem cell transplant. For an allogeneic stem cell transplant, after the bone marrow is destroyed, the patient receives blood-forming stem cells from another person, the donor. This is the type of transplant typically used for MDS. In an autologous stem cell transplant, the patients get back their own stem cells (which were removed before treatment). This type of transplant is not typically used for patients with MDS because the patient's bone marrow contains abnormal stem cells.
The chemotherapy segment is further segmented based on drug class such as hypomethylating agents, immunomodulatory drugs, and anti-anemics
MDS drugs are divided into the following therapeutic classes: hypomethylating agents, immunomodulatory drugs, and anti-anemics. Among these, the immunomodulatory drugs accounted for largets market share in 2019, due to growing adoption of therapeutics and lack of generic competition. Currently, Revlimid (lenalidomide) is the only one approved for treatment of low-risk MDS and myelodysplastic syndrome with isolated del(5q). Lenalidomide is considered an immunomodulatory agent. This means it is able to enhance the activity of immune cells and reduce inflammation. This slows the growth of abnormal bone marrow cells. In addition, it improves the way certain white blood cells work and is thought to slow the growth of new blood vessels that feed the MDS cells. Lenalidomide (Revlimid¬Æ) is approved for treating MDS patients with isolated del(5q) MDS subtyped who are transfusion dependent (still need blood transfusions) and have a low or intermediate-1 risk IPSS (International Prognostic Scoring System) score. Research studies are currently looking at how well lenalidomide works for patients with other MDS subtypes.
Hypomethylating agents such as Celgene's Vidaza and Otsuka's Dacogen are used as first-line treatment for patients with high-risk myelodysplastic syndrome. This segment is forecast to witness a steep fall in market share due to patent expirations of both the aforementioned drugs, which has led to the launch of several generics in the market.
In recent years, demand for hypomethylating agents has been at a high due to approval and adoption of Vidaza and Dacogen. A strong pipeline including Aranesp is expected to boost market growth in the near future. Easy availability and access to novel treatments in major countries provides strong commercial opportunities to the market. Azacitidine is in a class of medicines called hypomethylating agents. Drugs in this class help prevent the growth of abnormal bone marrow stem cells. Azacitidine was the first medicine approved by the U.S. Food and Drug Administration (FDA) specifically to treat MDS. It is approved to treat both low- and high-risk patients with all subtypes of MDS. Decitabine is in a class of medicines called hypomethylating agents. Drugs in this class help prevent the growth of abnormal bone marrow stem cells. Decitabine, like azacitidine, is approved by the U.S. Food and Drug Administration (FDA) specifically to treat MDS. It is approved to treat both low- and high-risk patients with all subtypes of MDS.
The anticipated launch of Celgene's luspatercept and Amgen's Aranesp in 2019 are projected to significantly fuel the anti-anemics drug segment. Both are under investigation in late-stage clinical trials for treatment of myelodysplastic syndrome. Recent study outcomes have demonstrated that they successfully increased RBC count in the blood, thus reducing need for frequent blood transfusions. Luspatercept-aamt is the first erythroid maturation agent (EMA) approved by the US Food and Drug Administration and European Union for the treatment of anemia in adult patients with myelodysplastic syndromes (MDS) who have been failed an erythropoiesis stimulating agent (ESA) or are unlikely to respond to an ESA, and are requiring transfusions of 2 or more red blood cell (RBC) units over 8 weeks.
Market Geographical Analysis
North America region is dominating the global myelodysplastic syndrome treatment market accounted for the largest market share in 2019, owing to rising prevalence, high R&D investments on the development of the novel drugs, and the presence of advanced healthcare infrastructure. It is one of the most common malignant haematological diseases that affects five out of every 100,000 people in the U.S. annually. An estimated 60,000 people in the U.S. live with MDS, and approximately 10,000-15,000 new cases are reported each year.
In December 2019, Bristol-Myers Squibb and Acceleron Pharma announced that the FDA Advisory Committee would review Reblozyl (luspatercept-aamt) for use in patients with myelodysplastic syndrome.
Asia-Pacific is expected to experience lucrative growth in the global myelodysplastic syndrome treatment market due to the developing healthcare infrastructure, rapidly improving economic conditions and a promising regulatory environment for new treatment. In September 2019, Astellas Pharma Inc. and FibroGen, Inc announced that Japan's Ministry of Health, Labour and Welfare (MHLW) approved Evrenzo® (generic name: roxadustat) for the treatment of anemia associated with chronic kidney disease (CKD) in dialysis patients. Roxadustat is also in Phase 3 clinical development in the U.S. and Europe and in Phase 2/3 development in China for anemia associated with myelodysplastic syndromes.
Market Competitive Landscape
The myelodysplastic syndrome (MDS) treatment market is moderately competitive and consists of several major players. Some of the key players which are contributing to the growth of the market include AbbVie, Otsuka America Pharmaceutical Inc., Accord Healthcare Ltd., Novartis, Bristol-Myers Squibb, Takeda Pharmaceutical Company Limited, Onconova Therapeutics, Celgene Corporation, Sandoz, Inc., Dr. Reddy's Laboratories, Inc., among others.
The major players are adopting several growth strategies such as product launches, acquisitions, and collaborations, which are contributing to the growth of the myelodysplastic syndrome (MDS) treatment market globally. For instance,
The global myelodysplastic syndrome (MDS) treatment market report would provide an access to an approx. 53 market data table, 45 figures and 250 pages.
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