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Historical Year
Forecast Year
The Global Atypical Teratoid Rhabdoid Tumours (ATRT) Treatment market is expected to grow at a CAGR of 7.9% during the forecast period of 2024-2032, driven by the growing awareness of rare diseases.
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Atypical Teratoid Rhabdoid (ATRT) is a primary tumour in the central nervous system (CNS). It begins in the brain or spinal cord. Primary CNS tumours are graded based on the location of the tumour, the type of tumour, the extent of tumour spread, genetic findings, the patient's age, and the amount of tumour that remains after surgery, if surgery is possible.
ATRTs are all considered Grade IV tumours. This indicates that they are malignant (cancerous) and rapidly growing. Cancer is a genetic disease, which means that it is caused by changes in genes that control how our cells function. In many types of cancer, genes can be mutated (changed), causing cancer cells to grow and spread.
Majority of ATRTs are caused by mutations in the SMARCB1 gene (also called INI1). This gene normally sends signals to proteins that inhibit tumour growth. SMARCB1 does not function properly in ATRTs, and tumour growth is uncontrolled. SM ARCB1 is sometimes found in a person's DNA, indicating that they are born with it. ATRTs can grow very quickly. They frequently spread to other areas of the CNS via cerebrospinal fluid (CSF).
The symptoms of an ATRT vary, depending on the location of the tumour and the age of the person. Some of the most common symptoms are as follows:
Symptoms usually worsen quickly as the ATRTs grow quickly.
According to the market research report, the atypical teratoid rhabdoid treatment market can be categorised into the following segments:
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Market Breakup by Treatment Method
Market Breakup by Route of Administration
Market Breakup by Treatment Channel
Market Breakup by Region
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ATRTs can occur likewise in children and adults but they are extremely rare in both the age groups. This tumour affects an estimated 596 people in the United States. ATRTs are more prevalent in men than in women.
The first line of treatment for an ATRT is surgery. The surgery aims at obtaining tissue to determine the tumour and its type and to remove the tumour to the largest extent without exacerbating the patient's symptoms.
Following surgery, people with ATRTs typically receive additional treatments, such as radiation, chemotherapy, or clinical trials. Clinical trials involving new chemotherapy, targeted therapy, or immunotherapy drugs may also be available as a treatment option. The patient's healthcare team decides on treatments based on the patient's age, remaining tumour after surgery, tumour type, and tumour location.
The population growing awareness of rare and genetic disorders is expected to drive the demand for the market. The number of leading pharmaceutical companies, with products in clinical trials for the treatment of atypical teratoid rhabdoid, will drive the market growth.
The growth of the market can be hampered by the small patient population available for clinical trials.
The report gives an in-depth analysis of the key players involved in the Global Atypical Teratoid Rhabdoid Tumours (ATRT) Treatment market, sponsors manufacturing the therapies, and putting them through trials to get FDA approvals. The companies included in the market are as follows:
REPORT FEATURES | DETAILS |
Base Year | 2023 |
Historical Period | 2017-2023 |
Forecast Period | 2024-2032 |
Scope of the Report |
Historical and Forecast Trends, Industry Drivers and Constraints, Historical and Forecast Market Analysis by Segment:
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Breakup by Treatment Method |
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Breakup by Route of Drug Administration |
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Breakup by Distribution Channel |
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Breakup by Region |
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Market Dynamics |
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Supplier Landscape |
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Companies Covered |
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*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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The market is likely to grow at a CAGR of 7.9% during the forecast period of 2024-2032.
The population growing awareness of rare and genetic disorders is expected to drive the demand for the treatment.
The treatment methods used in the market include surgery, chemotherapy, radiation, and targeted immunotherapy.
The different treatment methods include oral, parenteral, intravitreal, subretinal, topical, and molecule type.
The major regional markets include North America, Europe, Middle East and Africa, Asia Pacific, Latin America.
The treatment channels can be divided into public and private.
Small population available for the clinical trials will restrain the growth of the market.
ATRTs can occur in children and adults but they are extremely rare in both age groups. There have only been 50 adult cases reported. This tumour affects an estimated 596 people in the United States.
Atypical teratoid rhabdoid tumours (ATRTs) are the most common type of malignant brain tumour in children under the age of one year. They are most diagnosed in infants and toddlers as young as 1 or 2 years old. They account for about 1-2% of all paediatric brain tumours in children under the age of 16.
Takeda Pharmaceutical Company, Vyriad Inc, Novartis AG, Istari Oncology Inc., Secura Bio, Inc., Pfizer, Inc., Ipsen Pharma, and Exelixis, Inc., among others are the key players in the market.
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193/26/4 St.no.6, Ward Binh Hung Hoa, Binh Tan District, Ho Chi Minh City
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United States (Head Office)
30 North Gould Street, Sheridan, WY 82801
+1-415-325-5166
Australia
63 Fiona Drive, Tamworth, NSW
+61-448-061-727
India
C130 Sector 2 Noida, Uttar Pradesh 201301
+91-858-608-1494
Philippines
40th Floor, PBCom Tower, 6795 Ayala Avenue Cor V.A Rufino St. Makati City, 1226.
+63-287-899-028, +63-967-048-3306
United Kingdom
6 Gardner Place, Becketts Close, Feltham TW14 0BX, Greater London
+44-753-713-2163
Vietnam
193/26/4 St.no.6, Ward Binh Hung Hoa, Binh Tan District, Ho Chi Minh City
+84-865-399-124
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