Changes in survival over time for primary brain and other CNS tumors in the United States, 2004–2017 - Scorecard - MDSpire

Changes in survival over time for primary brain and other CNS tumors in the United States, 2004–2017

  • By

  • Gino Cioffi

  • Kristin A. Waite

  • Jacob L. Edelson

  • Carol Kruchko

  • Quinn T. Ostrom

  • Jill S. Barnholtz-Sloan

  • October 5, 2022

  • 0 min

Share

Clinical Scorecard: Trends in Survival Rates for Primary Brain and Central Nervous System Tumors in the United States from 2004 to 2017

At a Glance

CategoryDetail
ConditionPrimary malignant and non-malignant brain and central nervous system (CNS) tumors
Key MechanismsTumor histopathology, site, patient age, sex, race/ethnicity, and treatment patterns influence survival
Target PopulationIndividuals diagnosed with primary brain and CNS tumors in the United States, stratified by age groups (0–14, 15–39, 40+ years)
Care SettingOncology and neurosurgery centers managing brain and CNS tumors, including surgical, radiation, and chemotherapy treatment settings

Key Highlights

  • From 2001 to 2017, 5-year relative survival was 66.9% for malignant and 92.1% for non-malignant primary brain and CNS tumors.
  • Younger individuals (0–14 and 15–39 years) have higher 5-year survival rates compared to adults aged 40 years and older.
  • Survival varies widely by tumor site and histopathology, with pilocytic astrocytoma showing the best prognosis and glioblastoma the worst.

Guideline-Based Recommendations

Diagnosis

  • Use histopathologic or radiographic confirmation for tumor classification.
  • Classify tumors by behavior codes (ICD-O-3) and histopathology per WHO CNS tumor classification.
  • Consider patient age, tumor site, and histopathology for prognosis estimation.

Management

  • Initial treatment should include surgical resection; extent of resection is a positive prognostic factor for malignant tumors.
  • Combine radiation therapy with chemotherapy (e.g., temozolomide) for glioblastoma to improve survival.
  • Treatment plans should be individualized based on tumor type, patient age, and overall health.

Monitoring & Follow-up

  • Monitor survival outcomes over time using population-based registries and stratify by age, tumor type, and treatment received.
  • Assess treatment response and adjust management accordingly, especially in high-risk histopathologies.

Risks

  • Older adults (≥40 years) have poorer survival outcomes across most tumor subtypes.
  • Black non-Hispanic individuals generally have worse survival compared to non-Hispanic White individuals.
  • Glioblastoma carries a particularly poor prognosis despite treatment advances.

Patient & Prescribing Data

Patients with primary malignant and non-malignant brain and CNS tumors across all age groups in the US

Surgery remains the cornerstone of initial treatment; combined radiation and temozolomide therapy improves survival in glioblastoma; optimal treatment for many tumor types remains undetermined.

Clinical Best Practices

  • Stratify patients by age, tumor histopathology, and site to guide prognosis and treatment decisions.
  • Aim for maximal safe surgical resection to improve survival in malignant brain tumors.
  • Incorporate combined modality therapy (radiation plus chemotherapy) for glioblastoma based on evidence.
  • Utilize population-based cancer registries for ongoing survival monitoring and research.
  • Recognize demographic disparities in survival and tailor supportive care accordingly.

References

Original Source(s)

Related Content