The 7 major ewing’s sarcoma markets reached a value of US$ 47.8 Million in 2023. Looking forward, IMARC Group expects the 7MM to reach US$ 74.5 Million by 2034, exhibiting a growth rate (CAGR) of 4.1% during 2024-2034.
Report Attribute
|
Key Statistics
|
---|---|
Base Year |
2023
|
Forecast Years | 2024-2034 |
Historical Years |
2018-2023
|
Market Size in 2023
|
US$ 47.8 Million |
Market Forecast in 2034
|
US$ 74.5 Million |
Market Growth Rate (2024-2034)
|
4.1% |
The Ewing’s sarcoma market has been comprehensively analyzed in IMARC's new report titled "Ewing’s Sarcoma Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2024-2034". Ewing's sarcoma is a rare type of oncological disease that affects primitive nerve tissue of bones or soft tissues surrounding the bones. It most commonly occurs in the long bones of the arms and legs but can also develop in the soft tissues of the limbs, chest, or abdomen. Individuals suffering from this condition may experience pain, tenderness or swelling near the affected area, bone pain, limping, extreme tiredness, fever with no known cause, unexplained weight loss, etc. The other infrequent symptoms include palpable soft-tissue mass, paralysis, loss of bladder control, and bone fractures. The diagnosis of Ewing's sarcoma is mainly made by reviewing the patient's underlying indications, medical history, and physical examination. Numerous other studies, like magnetic resonance imaging (MRI), computed tomography (CT) scans, positron emission tomography (PET) scans, etc., are also utilized to look for signs of bone damage. The healthcare provider may further perform a biopsy, which involves the removal of tiny samples of the affected region to examine it under a microscope and validate a diagnosis.
The increasing cases of genetic abnormalities that lead to the disruption of normal tissues and the formation of unhealthy cells throughout the body are primarily driving the Ewing's sarcoma market. In addition to this, the widespread adoption of radical chemotherapy, which aims at complete irradiation of tumors, is also bolstering the market growth. Furthermore, the escalating demand for antisense oligodeoxynucleotide therapy to treat locally advanced disease conditions by down-regulating the expression of the oncogenic cellular RNA associated with the development of Ewing's sarcoma is acting as another significant growth-inducing factor. Additionally, the inflating utilization of proton beam radiation technique, which delivers an effective dose and controls damage to healthy tissues surrounding the cancerous cells, is further creating a positive outlook for the market. Apart from this, the emerging popularity of autologous stem cell transplantation as a viable treatment option owing to reduced metastasis and improved disease-free survival of patients, is expected to drive the Ewing's sarcoma market in the coming years.
IMARC Group's new report provides an exhaustive analysis of the Ewing’s sarcoma market in the United States, EU4 (Germany, Spain, Italy, and France), United Kingdom, and Japan. This includes treatment practices, in-market, and pipeline drugs, share of individual therapies, market performance across the seven major markets, market performance of key companies and their drugs, etc. The report also provides the current and future patient pool across the seven major markets. According to the report, the United States has the largest patient pool for Ewing’s sarcoma and also represents the largest market for its treatment. Furthermore, the current treatment practice/algorithm, market drivers, challenges, opportunities, reimbursement scenario, unmet medical needs, etc., have also been provided in the report. This report is a must-read for manufacturers, investors, business strategists, researchers, consultants, and all those who have any kind of stake or are planning to foray into the Ewing’s sarcoma market in any manner.
Lurbinectedin, also called PM01183, or commercially where approved as Zepzelca, is used for the treatment of Ewing's sarcoma. Lurbinectedin suppresses active transcription of protein-coding genes by binding to promoters and irreversibly delaying elongating RNA polymerase II on the DNA template, causing double-stranded DNA breaks and death.
Vigil is a personalized immunotherapy platform that combines a unique bi-shRNA DNA plasmid with the patient's tumor tissue to achieve immunological anticancer action. The Trifecta of systemic action entails inhibiting tumor suppressor cytokines TGFβ1 and TGFβ2, increasing GMCSF expression to improve local immune function, and presenting clonal neoantigen epitopes using autologous cancer tissue. Vigil uses the patient's tumor as an antigen source to trigger an immune response tailored to their specific clonal tumor neoantigens.
Seclidemstat (SP-2577) is a differentiated inhibitor of LSD1, a well-established target for both hematological and solid malignancies. SP-2577 inhibits LSD1's enzymatic activity and scaffolding role.
Time Period of the Study
Countries Covered
Analysis Covered Across Each Country
This report also provides a detailed analysis of the current Ewing’s sarcoma marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
---|---|
Lurbinectedin | PharmaMar |
Vigil | Gradalis |
Seclidemstat | Salarius Pharmaceuticals |
Eribulin mesylate | Eisai Co Ltd |
*Kindly note that the drugs in the above table only represent a partial list of marketed/pipeline drugs, and the complete list has been provided in the report.
Market Insights
Epidemiology Insights
Ewing’s Sarcoma: Current Treatment Scenario, Marketed Drugs and Emerging Therapies