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Chemotherapy Brain Tumor Success Rate: Survival Statistics and Factors Influencing Prognosis

What are the survival rates for brain and spinal cord tumors. How does tumor type, grade, and location affect prognosis. What factors influence brain tumor treatment outcomes and patient survival.

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Understanding Brain Tumor Survival Statistics

Brain and spinal cord tumors encompass a diverse group of conditions with varying prognoses. While general statistics provide insight into overall trends, it’s crucial to understand that individual outcomes can differ significantly. Survival rates are typically measured in terms of 1-year and 5-year intervals, but these figures don’t necessarily indicate a specific life expectancy.

The Office for National Statistics (ONS) and researchers collect data on cancer patients to analyze survival rates. The 5-year survival rate refers to the percentage of patients who are still alive 5 years after their initial diagnosis. However, it’s important to note that many patients live well beyond this timeframe.

General Survival Statistics for Malignant Brain Tumors

For individuals diagnosed with cancerous (malignant) brain tumors in England:

  • 40% survive for 1 year or more after diagnosis
  • More than 10% survive for 5 years or more after diagnosis

These figures are based on net survival, which estimates the number of people who survive their cancer while accounting for other potential causes of death.

Factors Influencing Brain Tumor Survival Rates

Several key factors contribute to the prognosis and survival rates of brain and spinal cord tumors. Understanding these elements can provide valuable insight into potential treatment outcomes and overall patient outlook.

Tumor Type and Grade

Different types of brain tumors respond variably to treatment modalities. Some may be more susceptible to radiotherapy, while others might require alternative approaches. The grade of the tumor, which indicates its growth rate and aggressiveness, is often a critical prognostic factor.

How does tumor grade affect prognosis? Generally, high-grade tumors (fast-growing) have a higher likelihood of recurrence after treatment compared to low-grade tumors (slow-growing). However, the impact of grade can vary depending on the specific tumor type.

Biomarkers and Genetic Factors

Advancements in molecular diagnostics have led to the identification of certain genetic changes, or biomarkers, within tumor cells. These biomarkers can provide valuable information about a tumor’s behavior and potential response to treatment.

What role do biomarkers play in treatment decisions? Doctors use biomarker and molecular studies to tailor treatment approaches, helping to predict which tumors are more likely to respond to specific therapies. This personalized approach can significantly impact patient outcomes.

Tumor Location and Size

The position of a brain tumor within the cranial cavity can greatly influence treatment options and overall prognosis. Tumors located in certain areas, such as near the optic nerves, brain stem, or major blood vessels, may be more challenging to treat surgically.

How does tumor size impact treatment decisions? Larger tumors or those with ill-defined borders may be more difficult to remove completely. Conversely, small, well-defined tumors are often more amenable to surgical intervention. The shape and consistency of the tumor can also affect the ease of removal.

Age and General Health Considerations

A patient’s age and overall health status at the time of diagnosis play significant roles in determining prognosis and treatment outcomes for brain tumors.

Impact of Age on Prognosis

Research indicates that younger patients often have more favorable prognoses when it comes to brain tumors. Specifically, individuals under the age of 40 tend to have better outcomes compared to older patients.

Why do younger patients often fare better? Younger individuals may have greater physiological reserves and ability to withstand aggressive treatments. Additionally, certain tumor types are more common in specific age groups, which can influence overall survival statistics.

General Health and Treatment Tolerance

A patient’s overall health and fitness level can significantly impact their ability to tolerate and respond to brain tumor treatments.

How does general health affect treatment outcomes? Patients in good physical condition may recover more quickly from surgical interventions and experience fewer complications during chemotherapy or radiation treatments. This can lead to more successful treatment courses and potentially improved survival rates.

Treatment Modalities and Their Impact on Survival

The choice of treatment modality for brain tumors depends on various factors, including tumor type, location, and patient characteristics. Understanding the role of different treatments can provide insight into potential outcomes.

Surgical Intervention

Surgery is often the primary treatment for many types of brain tumors. The extent of tumor removal can significantly impact prognosis.

What factors determine surgical success? The location and accessibility of the tumor play crucial roles. Tumors in easily accessible areas of the brain may be more amenable to complete resection, potentially improving outcomes. However, tumors in critical or hard-to-reach areas may require more conservative approaches.

Radiation Therapy

Radiation therapy is commonly used in conjunction with surgery or as a primary treatment for certain brain tumors.

How effective is radiation therapy for brain tumors? The efficacy of radiation can vary depending on the tumor type and grade. Some tumors are more radiosensitive than others, responding better to this treatment modality. Advances in targeted radiation techniques have also improved outcomes for many patients.

Chemotherapy

Chemotherapy plays a vital role in the treatment of many brain tumors, either as a primary treatment or in combination with other modalities.

What factors influence chemotherapy success rates? The effectiveness of chemotherapy can depend on the specific tumor type, its genetic profile, and the ability of drugs to penetrate the blood-brain barrier. Some tumors may be more chemosensitive than others, leading to better treatment responses.

Emerging Therapies and Future Directions

The field of neuro-oncology is rapidly evolving, with new treatment approaches showing promise for improving brain tumor survival rates.

Immunotherapy

Immunotherapy, which harnesses the power of the body’s immune system to fight cancer, is an area of active research in brain tumor treatment.

What potential does immunotherapy hold for brain tumor treatment? Early studies have shown promising results for certain types of brain tumors, particularly in combination with other treatment modalities. However, more research is needed to fully understand its efficacy and identify the patients most likely to benefit.

Targeted Therapies

Advances in molecular profiling have led to the development of targeted therapies designed to attack specific genetic alterations within tumor cells.

How might targeted therapies improve brain tumor outcomes? By focusing on the specific molecular drivers of tumor growth, these therapies have the potential to be more effective and less toxic than traditional chemotherapy. Ongoing clinical trials are exploring various targeted agents for different brain tumor types.

Quality of Life Considerations

While survival rates are important, it’s equally crucial to consider quality of life factors when discussing brain tumor outcomes.

Neurological Function and Rehabilitation

Brain tumors and their treatments can impact various aspects of neurological function, including cognition, motor skills, and sensory perception.

What role does rehabilitation play in brain tumor recovery? Comprehensive rehabilitation programs, including physical therapy, occupational therapy, and speech therapy, can significantly improve functional outcomes and quality of life for brain tumor patients. Early intervention and ongoing support are key to maximizing recovery potential.

Psychosocial Support

The emotional and psychological impact of a brain tumor diagnosis and treatment can be significant for both patients and their families.

How can psychosocial support improve outcomes? Access to mental health services, support groups, and counseling can help patients and caregivers cope with the challenges of brain tumor treatment and recovery. Addressing psychological well-being may indirectly contribute to better overall outcomes by improving treatment adherence and quality of life.

Importance of Individualized Care

While general statistics provide valuable insights, it’s crucial to remember that each brain tumor case is unique. Personalized treatment approaches that consider individual patient factors are essential for optimizing outcomes.

Multidisciplinary Care Teams

The complexity of brain tumor management often requires input from various medical specialties.

Why is a multidisciplinary approach important? Collaboration between neurosurgeons, neuro-oncologists, radiation oncologists, and other specialists ensures comprehensive care that addresses all aspects of a patient’s condition. This approach can lead to more effective treatment strategies and improved overall outcomes.

Ongoing Monitoring and Adaptable Treatment Plans

Brain tumor management often requires long-term follow-up and the ability to adjust treatment strategies as needed.

How does ongoing monitoring impact survival rates? Regular imaging and clinical assessments allow for early detection of tumor recurrence or treatment-related complications. This proactive approach enables timely interventions that may improve long-term survival and quality of life.

In conclusion, while brain tumor survival rates have improved over the years, there is still much work to be done. Ongoing research into new treatment modalities, improved understanding of tumor biology, and personalized care approaches offer hope for continued advancements in brain tumor outcomes. Patients and their families should work closely with their healthcare teams to understand their specific prognosis and explore all available treatment options.

Survival for brain and spinal cord tumours

Survival for brain and spinal cord tumours depends on different factors. So no one call tell you exactly how long you will live.

These are general statistics based on large groups of people. Remember, they can’t tell you what will happen in your individual case.

Your doctor or specialist nurse can give you more information about your own outlook (prognosis).

You can also talk about this with the Cancer Research UK nurses on freephone 0808 800 4040, from 9am to 5pm, Monday to Friday.

Survival is different for adults and children with brain and spinal cord tumours. This page is for adults with cancerous (malignant) and non cancerous (benign) brain tumours. 

We have separate information about survival for children with brain tumours.

About these statistics

The terms 1 year survival and 5 year survival don’t mean that you will only live for 1 or 5 years.

The Office for National Statistics (ONS) and researchers collect information. They watch what happens to people with cancer in the years after their diagnosis. 5 years is a common time point to measure survival. But some people live much longer than this.

5 year survival is the number of people who have not died from their cancer within 5 years after diagnosis.

What affects survival

Brain tumours are quite rare and there are many different types. Survival depends on many factors.

Type of tumour

Different types of brain tumours respond differently to treatment. Some respond better to radiotherapy than others, for example. Some types are likely to spread into the surrounding brain tissue or down the spinal cord. This might make them difficult to remove with surgery.

Grade of the tumour 

The grade is one of the most important factors for some types of tumours. But for others, the grade is much less likely to predict how the tumour might behave. Generally, fast growing (high grade) tumours are much more likely to come back after treatment than slow growing (low grade) tumours.

Biomarkers

Your doctor looks to see if there are certain gene changes in the cells of some types of brain tumours. These tests are also called biomarker or molecular studies. 

The results of these tests help the doctors work out how your tumour might behave. They also help them see how likely it is that the tumour will respond to treatment. 

Position in the brain

The type of treatment you have might depend on where the tumour is in your brain. For example, surgery is the main treatment for most types of brain tumour. But some parts of the brain are more difficult to operate on than others. These include areas near the nerves that control your sight (optic nerves), the brain stem, spinal cord, or areas close to major blood vessels.

Sometimes the tumour may be in an area where it isn’t possible for doctors to operate on. For tumours in these areas, radiotherapy or chemotherapy may be better options for treatment.  

Size or shape of the brain tumour

It might be more difficult to remove large tumours, or those where the edge of the tumour is not clear. Small, firm and rounded tumours are easier to remove. It is also easier for surgeons to remove tumours that start in the lining of the brain and spinal cord.  

Age and general health at diagnosis

Your prognosis is better if you are younger than 40. Your general health can also affect your prognosis. If you are very fit and healthy, you are likely to recover quicker from treatment. 

Survival for all types of cancerous (malignant) brain tumour

Generally for people with a cancerous (malignant) brain tumour in England:

  • 40 out of 100 people (40%) survive their cancer for 1 year or more
  • more than 10 out of 100 people (more than 10%) survive their cancer for 5 years or more

Where this information comes from

Cancer survival by stage at diagnosis for England, 2019
Office for National Statistics

These figures are for people diagnosed in England between 2013 and 2017.  

These statistics are for net survival. Net survival estimates the number of people who survive their cancer rather than calculating the number of people diagnosed with cancer who are still alive. In other words, it is the survival of cancer patients after taking into account that some people would have died from other causes if they had not had cancer.

Survival for the different types of malignant brain tumours

The following statistics are for different types of brain tumours that can be cancerous (malignant).

Please note, some of the tumours included in the list below can also be non cancerous (benign).

Doctors use a system to group (classify) brain tumours into different types. The World Health Organisation (WHO) regularly updates this system. Doctors have changed how they group some brain tumour types following the latest WHO classification in 2021.

These updates can make it challenging to present survival statistics. The available survival data is based on patients diagnosed using older classification systems. It takes time for doctors to start using the new classification systems. And cancer registries also need to update their data collection systems.

Astrocytoma and glioblastoma

The way doctors classify astrocytomas and glioblastomas has changed. The survival data below is for patients diagnosed using an older WHO classification system. Your doctor or specialist nurse can help you understand which statistics are most relevant for your situation.

Below, we provide statistics for:

  • grade 2 astrocytoma, which is sometimes called diffuse astrocytoma
  • grade 3 astrocytoma, which is sometimes called anaplastic astrocytoma
  • glioblastoma (which used to be called grade 4 astrocytoma)

The following statistics are from a large international study. This collected survival statistics for people in 59 different countries including the UK. The study looked at people diagnosed with brain tumours between 2000 and 2014. The following figures are for people in the UK, diagnosed between 2010 and 2014:

For diffuse astrocytoma (grade 2 astrocytoma):

  • 45 out of 100 people (45%) survive their brain tumour for 5 years or more

For anaplastic astrocytoma (grade 3 astrocytoma):

  • more than 20 out of 100 people (more than 20%) survive their brain tumour for 5 years or more

For glioblastoma:

  • more than 5 out of 100 people (more than 5%) survive their brain tumour for 5 years or more

Where this information comes from

CONCORD Working Group. Global survival trends for brain tumors, by histology: analysis of individual records for 556,237 adults diagnosed in 59 countries during 2000-2014 (CONCORD-3).
F Girardi and others
Neuro Oncology, 2023 Volume 25, Issue 3, Pages 580-592

These statistics are for Net survival. Net survival estimates the number of people who survive their cancer rather than calculating the number of people diagnosed with cancer who are still alive. In other words, it is the survival of cancer patients after taking into account that some people would have died from other causes if they had not had cancer.

Ependymoma

The following statistics come from the Central Brain Tumour Registry of the United States (CBTRUS). This report looked at children and adults diagnosed with a brain tumour in America between 2014 and 2018.

Please be aware that due to differences in health care systems, data collection and the population, these figures are not a true picture of survival in the UK.

For all types of ependymoma in the brain and spinal cord:

  • around 90 out of 100 people (around 90%) survive their cancer for 5 years or more
  • more than 85 out of 100 people (more than 85%) survive their cancer for 10 years or more

Ependymomas can be cancerous (malignant) or not cancerous (benign).

For malignant ependymomas:

  • around 85 out of 100 people (around 85%) survive their brain tumour for 5 years or more

For benign ependymomas:

  • around 95 out of 100 people (around 95%) survive their brain tumour for 5 years or more

Where this information comes from

CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2014-2018
Q Ostrom and others
Neuro Oncology 2021, Volume 23, Issue 12, Supplement 2, Pages 1 -105

These statistics are for relative survival. Relative survival takes into account that some people die of causes other than cancer. This gives a more accurate picture of cancer survival.

Oligodendroglioma

The following statistics are from a large international study. This collected survival statistics for people with brain tumours in 59 different countries including the UK. The study looked at people diagnosed between 2000 and 2014. The following figures are for people in the UK, diagnosed between 2010 and 2014:

For all grades of oligodendroglioma:

  • almost 55 out of 100 people (almost 55%) survived their brain tumour for 5 years or more

Where this information comes from

CONCORD Working Group. Global survival trends for brain tumors, by histology: analysis of individual records for 556,237 adults diagnosed in 59 countries during 2000-2014 (CONCORD-3).
F Girardi and others
Neuro Oncology 2023, Volume 25, Issue 3, Pages 580-592

These statistics are for Net survival. Net survival estimates the number of people who survive their cancer rather than calculating the number of people diagnosed with cancer who are still alive. In other words, it is the survival of cancer patients after taking into account that some people would have died from other causes if they had not had cancer.

Meningioma

Meningiomas can start in the brain or the spinal cord. Most meningiomas start in the brain (cranial meningiomas).

Doctors group meningiomas into groups based on how quickly they are likely to grow (the grade). Most meningiomas are grade 1 or grade 2. These are non cancerous (benign) tumours. They can also be grade 3 but this is rare. Grade 3 tumours are cancerous (malignant).

There are no UK wide survival statistics for meningioma. The information below is from people diagnosed with a cranial (brain) meningioma in England between 1999 and 2013:

  • almost 70 out of 100 people (almost 70%) with a grade 1 or grade 2 brain meningioma survive their cancer for 10 years or more
  • around 40 out of 100 people (around 40%) with a grade 3 brain meningioma survive their cancer or 10 years or more

Where this information comes from

Epidemiology of Meningiomas in England
T Karabatsou and others
On behalf of the National Cancer Registration and Analysis Service (NCRAS)

These statistics for people with meningioma are for relative survival. Relative survival takes into account that some people die of causes other than cancer. This gives a more accurate picture of cancer survival.

Embryonal tumours

Embryonal tumours develop from cells that are leftover from the early stages of our development. Until recently, doctors talked about embryonal tumours as primitive neuro ectodermal tumours (PNETs). There are different types of embryonal tumours including medulloblastomas and neuroblastomas.  

There are no UK wide statistics for survival for these tumours. The following statistics are from the Central Brain Tumour Registry of the United States (CBTRUS). This report looked at children and adults diagnosed with a brain tumour in America between 2014 and 2018.

Please be aware that due to differences in health care systems, data collection and the population, these figures are not a true picture of survival in the UK.

For embryonal tumours in people aged 15 to 39:

  • around 70 out of 100 people (around 70%) survive their brain tumour for 5 years or more
  • 60 out of 100 people (60%) survive their brain tumour for 10 years or more

For embryonal tumours in people aged 40 or older:

  • 45 out of 100 people (45%) survive their brain tumour for 5 years or more
  • more than 35 out of 100 people (more than 35%) survive their brain tumour for 10 years or more

Where this information comes from

CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2014-2018
Q Ostrom and others
Neuro Oncology 2021, Volume 23, Issue 12, Supplement 2, Pages 1 to 105

These statistics are for relative survival. Relative survival takes into account that some people die of causes other than cancer. This gives a more accurate picture of cancer survival.

Pineal region tumours

There are many types of tumours that start in the pineal region. The outlook for these tumours depends on the type of tumour you have.

There are no UK statistics for survival for these tumours. The following statistics come from the Central Brain Tumour Registry of the United States (CBTRUS). This report looked at children and adults diagnosed with a brain tumour in America between 2014 and 2018.

Please be aware that due to differences in health care systems, data collection and the population, these figures are not a true picture of survival in the UK.

For all pineal region tumours:

  • 80 out of 100 people (80%) survive their brain tumour for 5 years or more
  • almost 75 out of 100 people (almost 75%) survive their brain tumour for 10 years or more

Pineal region tumours can be cancerous (malignant) or non-cancerous (benign).

For malignant pineal region tumours:

  • almost 75 out of 100 people aged 15 to 39 (almost 75%) survive their brain tumour for 5 years or more
  • 70 out of 100 people aged 40 or older (70%) survive their brain tumour for 5 years or more

For benign pineal region brain tumours:

  • more than 95 out of 100 people aged 15 to 39 (more than 95%) survive their brain tumour for 5 years or more
  • more than 85 out of 100 people aged 40 or older (more than 85%) survive their brain tumour for 5 years or more

Where this information comes from

CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2014-2018
Q Ostrom and others
Neuro Oncology 2021, Volume 23, Issue 12, Supplement 2, Pages 1 to 105

These statistics are for relative survival. Relative survival takes into account that some people die of causes other than cancer. This gives a more accurate picture of cancer survival.

Spinal cord tumours

There are different types of spinal cord tumours. The most common types are meningiomas, tumours of the spinal nerves and ependymomas. Spinal cord tumours can be cancerous (malignant) or non cancerous (benign). Benign tumours have a better prognosis than malignant tumours.

There are no statistics in the UK for survival of all types of spinal cord tumours. The following statistics come from the Central Brain Tumour Registry of the United States (CBTRUS). This report looked at children and adults diagnosed with a brain and spinal tumour in America between 2014 and 2018.

Please be aware that due to differences in health care systems, data collection and the population, these figures are not a true picture of survival in the UK.

Generally, for people with malignant and benign spinal cord tumours:

  • almost 95 out of 100 people (almost 95%) survive their spinal cord tumour for 5 years or more
  • around 90 out of 100 people (around 90%) survive their spinal cord tumour for 10 years or more 

Where this information comes from

CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2014-2018
Q Ostrom and others
Neuro Oncology 2021, Volume 23, Issue 12, Supplement 2, Pages 1 to 105

These statistics are for relative survival. Relative survival takes into account that some people die of causes other than cancer. This gives a more accurate picture of cancer survival.

Lymphoma of the brain or spinal cord

Lymphoma of the brain or spinal cord is also known as primary central nervous system (CNS) lymphoma.

There are no UK statistics for primary CNS lymphoma survival. The following statistics come from the Central Brain Tumour Registry of the United States (CBTRUS). This report looked at children and adults diagnosed with a brain tumour in America between 2014 and 2018.

Please be aware that due to differences in health care systems, data collection and the population, these figures are not a true picture of survival in the UK.

For primary CNS lymphoma:

  • almost 40 out of 100 people (almost 40%) survive their lymphoma for 5 years or more
  • around 30 out of 100 people (around 30%) survive their lymphoma for 10 years or more

Where this information comes from

CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2014-2018
Q Ostrom and others
Neuro Oncology 2021, Volume 23, Issue 12, Supplement 2, Pages 1 to 105

These statistics are for relative survival. Relative survival takes into account that some people die of causes other than cancer. This gives a more accurate picture of cancer survival.

Survival for different types of non cancerous (benign) brain tumours

The following statistics are for brain tumours that are usually non cancerous (benign):

Vestibular Schwannoma (acoustic neuroma)

Vestibular schwannoma is the most common type of non cancerous (benign) nerve sheath tumour. Survival statistics are available for nerve sheath tumours, from the Central Brain Tumour Registry of the United States (CBTRUS). This report looked at people diagnosed with a brain tumour in America between 2014 and 2018.

Please be aware that due to differences in health care systems, data collection and the population, these figures are not a true picture of survival in the UK.

For benign nerve sheath tumours:

  • 99 out of 100 (99%) people survive their tumour for 5 years or more 

Where this information comes from

CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2014-2018
Q Ostrom and others
Neuro Oncology 2021, Volume 23, Issue 12, Supplement 2, Pages 1 to 105

These statistics for adults with benign nerve sheath tumours, diagnosed between 2001 and 2017. They are for relative survival. Relative survival takes into account that some people die of causes other than cancer. This gives a more accurate picture of cancer survival.

Pituitary tumours

Most pituitary tumours are non cancerous (benign). Benign pituitary gland tumours are also called pituitary adenomas.

There are no UK survival statistics for these tumours. The following statistics come from the Central Brain Tumour Registry of the United States (CBTRUS). This report looked at children and adults diagnosed with a brain tumour in America between 2014 and 2018.

Please be aware that due to differences in health care systems, data collection and the population, these figures are not a true picture of survival in the UK.

For all pituitary gland tumours:

  • more than 95 out of 100 people (more than 95%) survive their brain tumour for 5 years or more
  • 95 out of 100 people (95%) survive their brain tumour for 10 years or more

Where this information comes from

CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2014-2018
Q Ostrom and others
Neuro Oncology 2021, Volume 23, Issue 12, Supplement 2, Pages 1 to 105

These statistics are for relative survival. Relative survival takes into account that some people die of causes other than cancer. This gives a more accurate picture of cancer survival.

Haemangioblastoma

Haemangioblastomas are rare slow growing tumours. The following statistics come from the Central Brain Tumour Registry of the United States (CBTRUS). This report looked at children and adults diagnosed with a brain tumour in America between 2014 and 2018.

Please be aware that due to differences in health care systems, data collection and the population, these figures are not a true picture of survival in the UK.

Haemangioblastomas are a type of haemangioma. For haemangiomas:

  • 95 out of 100 people (95%) survive their tumour for 5 years or more
  • almost 95 out of 100 people (almost 95%) survive their tumour for 10 years or more

Where this information comes from

CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2014-2018
Q Ostrom and others
Neuro Oncology 2021, Volume 23, Issue 12, Supplement 2, Pages 1 to 105

These statistics are for relative survival. Relative survival takes into account that some people die of causes other than cancer. This gives a more accurate picture of cancer survival.

Craniopharyngioma

Craniopharyngiomas are tumours that grow near the base of the brain. These tumours do not usually spread and have a good prognosis.

The following statistics come from the Central Brain Tumour Registry of the United States (CBTRUS). This report looked at children and adults diagnosed with a brain tumour in America between 2014 and 2018.

Please be aware that due to differences in health care systems, data collection and the population, these figures are not a true picture of survival in the UK.

For craniopharyngiomas:

  • around 85 out of 100 people (around 85%) survive their tumour for 5 years or more
  • 80 out of 100 people (80%) survive their tumour for 10 years or more

Where this information comes from

CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2014-2018
Q Ostrom and others
Neuro Oncology 2021, Volume 23, Issue 12, Supplement 2, Pages 1 to 105

These statistics are for relative survival. Relative survival takes into account that some people die of causes other than cancer. This gives a more accurate picture of cancer survival.

More statistics

  • The 2021 WHO Classification of Tumors of the Central Nervous System: a summary.
    D Louis and others
    Neuro Oncology, 2021 Volume 23, Issue 8, Pages 1231-1251

  • CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2014-2018
    Q Ostrom and others
    Neuro Oncology 2021, Volume 23, Issue 12, Supplement 2, Pages 1 to 105

  • Cancer survival by stage at diagnosis for England, 2019
    Office for National Statistics

  • Epidemiology of Meningiomas in England
    T Karabatsou and others
    On behalf of the National Cancer Registration and Analysis Service (NCRAS)

  • CONCORD Working Group. Global survival trends for brain tumors, by histology: analysis of individual records for 556,237 adults diagnosed in 59 countries during 2000-2014 (CONCORD-3).
    F Girardi and others
    Neuro Oncol. 2023 Volume 25, issue 3, pages 580-592

  • The information on this page is based on literature searches and specialist checking. We used many references and there are too many to list here. Please contact [email protected] with details of the particular issue you are interested in if you need additional references for this information.

Last reviewed: 

16 Jun 2023

Next review due: 

16 Jun 2026

Type of Tumor

5-Year Relative Survival Rate

Age

20-44

45-54

55-64

Low-grade (diffuse) astrocytoma

73%

46%

26%

Anaplastic astrocytoma

58%

29%

15%

Glioblastoma

22%

9%

6%

Oligodendroglioma

90%

82%

69%

Anaplastic oligodendroglioma

76%

67%

45%

Ependymoma/anaplastic ependymoma

92%

90%

87%

Meningioma

84%

79%

74%