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Dr. Amit Vatkar
MBBS, DCH, DNB Pediatrics
Fellow in Pediatric Neurology, Mumbai
Trained in Neurophysiology & Epilepsy, USA
Contact No. : +91-8767844488
Email: vatkaramit@yahoo.com
MANAGEMENT OF
CHILDHOOD BRAIN
TUMORS
INVESTIGATIONS
• Routine Investigations
• X-ray of Skull
Hydrocephalus – Sutural diastasis,erosion of
posterior clinoid,
Beaten silver appearance
Calcifications – Craniopharyngioma,
ependymoma,
Oligodendroglioma
• CT Brain
- Less time consuming
- Calcifications
• MRI Brain
- Better delineation of tumors
- Highly sensitive for brain stem and posterior fossa tumors
- No radiation hazard
Pilocytic astrocytoma
CT scan
Mri Plain MRI Contrast
EPENDYOMA
EPENDYOMA CT
MRI PLAIN
MRI CONTAST
MEDULLOBLASTOMA MRI PLAIN
MEDULLOBLASTOMA MRI COTRAST
CRANIOPHARYMGIOMA CT
CRANIOPHAYRNGIOMA MRI PLAIN
• CRANIOPHAYRNGIOMA MRI PLAIN
CRANIOPHAYRNGIOMA MRI CONTRAST
CHOROID PLEXUS PAPILLOMA CT
PLAIN CHOROID PLEXUS PAPILLOMA CT CONTRAST
PONTINE GLIOMA CT PLAIN PONTINE GLIOMA CT CONTRAST
• CSF analysis – Medulloblastoma, Ependymoma
Germ cell tumors
• Immunopositivity - transthyretin (prealbumin) positive in choroid
plexus tumors
• AFP & Beta HCG - In serum and CSF for germ cell tumors
• Endocrine evaluation - craniopharyngiomas
• MR spectroscopy,PET,SPECT scan – variation in the metabolism of
Tumors cells and normal brain tissue
• Myelography
• Biopsy
TREATMENT
• Supportive
• Specific
Surgery
Radiotherapy
Chemotherapy
 Newer techniques
Supportive
Measures to reduce ICP
• Head elevation
• Hyperventilation
• Hypothermia
• Osmotic diuretics – 20% mannitol 0.25g/kg
• Corticosteroids – 0.1 to 0.2mg/kg 6th hrly
• Acetazolamide & frusemide
- Anticonvulsive drugs – phenobarbitone
- Shunting procedures for Hydrocephalus
Specific
• Surgery
- Primary modality of treatment
- Good prognosis if complete surgical removal is possible. Pilocytic
Astrocytoma, Choroid plexus papilloma
- Not possible in pontine glioma, Germ cell tumors and pineal tumors
• Radiotherapy:
- Tumor cannot be removed surgically
- Residual tumor
- Craniospinal irradiation – Medulloblastoma,
Ependymoma,Germ
Cell tumors,
Pineoblastoma
- Avoid <4yrs
• Chemotherapy:
- Adjuvant therapy to surgery
- In children <4yrs to delay radiotherapy
- Some chemosensitive tumors – Pineal tumors, Medulloblastoma,
ependymoma, Astrocytoma
Newer techniques
• Steriotactic radiosurgery
• Intensity modulated radiation therapy
• Gene therapy – high grade gliomas
• High dose chemotherapy
• Growth factor inhibitors
• Angiogenesis inhibitors
• Radiosensitizers
• Immunotherapy
PROGNOSIS
• Size and location of the tumor
• Grade of tumor
• Age of child
• Metastasis at diagnosis
• Residual tumors
Name & location
of cells
Survival Rates Treatment
Medulloblastoma
(cerebellum)
50 percent after
five years
Surgery, radiation, chemotherapy, clinical trials.
Recurrent cancer: Stem cell transplant.
Cerebellar astrocytoma
(cerebellum)
90 percent after
five years
Surgery, radiation after repeat surgical
procedures.
Recurrent cancer: Surgery first, then radiation,
chemotherapy only if surgery and radiation are
not working, clinical trials.
Infratentorial ependymoma
(fourth ventricle
and spinal cord cavity)
50 percent after
five years
Surgery and radiation following, possible use of
chemotherapy for young children.
Recurrent cancer: Poor response to surgery and
radiotherapy, cisplatin chemotherapy works for
one third of patients, clinical trails should be
considered.
Brain stem glioma
(brain stem)
Most patients
die in 18 months
Usually cannot be surgically removed; use
radiation, not chemotherapy except for children
under three to delay radiation.
Recurrent cancer: No surgery, no chemotherapy
and no radiation, maximum has already been
administered. Clinical drug trials are only
option.
Name & location
of cells
Survival Rates Treatment
Cerebral astrocytoma, low
grade (cerebrum)
Over 80 percent
after five years
Surgery, radiation and chemotherapy only if
not surgically removed.
Recurrent cancer: Chemotherapy after
maximum surgery and radiation, clinical trials.
Cerebral astrocytoma,
high grade (cerebrum)
20-50 percent
after five years
Surgery, radiation and chemotherapy.
Chemotherapy is used for children under three
to delay radiation.
Recurrent cancer: Chemotherapy after
radiation, clinical trials.
Supratentorial
ependymoma
(back of the brain and
adjacent ventricles)
50 percent after
five years
Surgery followed by radiation. Chemotherapy
to delay radiation for very young children.
Recurrent cancer: Seldom controlled after
surgery and radiation. Cisplatin chemotherapy
works for one-third of patients. Clinical trails
should be considered.
Craniopharyngioma (benign
tumors
in the central
brain tissue)
Unknown Surgery is usually successful. Recurrent
cancer: Radiation.
Name & location
of cells
Survival Rates Treatment
Intracranial germ cell
tumor
Variable No surgery. Chemotherapy and radiation.
Recurrent cancer: Chemotherapy, clinical
trials.
Recurrent cancer: Chemotherapy, clinical
trials.
Pineal tumors
(pineal gland,
undifferentiated cells)
50 percent after
five years
Radiation and chemotherapy. Surgery is not
possible. Chemotherapy to delay radiation
for very young children.
Optic tract glioma (optic
nerves,
create visual symptoms)
Unknown For younger children: chemotherapy, then
radiation if chemo fails. Radiation earlier for
older children. Observation.
THANK YOU

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Management of Childhood Brain Tumors

  • 1. Dr. Amit Vatkar MBBS, DCH, DNB Pediatrics Fellow in Pediatric Neurology, Mumbai Trained in Neurophysiology & Epilepsy, USA Contact No. : +91-8767844488 Email: vatkaramit@yahoo.com MANAGEMENT OF CHILDHOOD BRAIN TUMORS
  • 2. INVESTIGATIONS • Routine Investigations • X-ray of Skull Hydrocephalus – Sutural diastasis,erosion of posterior clinoid, Beaten silver appearance Calcifications – Craniopharyngioma, ependymoma, Oligodendroglioma
  • 3. • CT Brain - Less time consuming - Calcifications • MRI Brain - Better delineation of tumors - Highly sensitive for brain stem and posterior fossa tumors - No radiation hazard
  • 7. CRANIOPHARYMGIOMA CT CRANIOPHAYRNGIOMA MRI PLAIN • CRANIOPHAYRNGIOMA MRI PLAIN CRANIOPHAYRNGIOMA MRI CONTRAST
  • 8. CHOROID PLEXUS PAPILLOMA CT PLAIN CHOROID PLEXUS PAPILLOMA CT CONTRAST
  • 9. PONTINE GLIOMA CT PLAIN PONTINE GLIOMA CT CONTRAST
  • 10. • CSF analysis – Medulloblastoma, Ependymoma Germ cell tumors • Immunopositivity - transthyretin (prealbumin) positive in choroid plexus tumors • AFP & Beta HCG - In serum and CSF for germ cell tumors • Endocrine evaluation - craniopharyngiomas
  • 11. • MR spectroscopy,PET,SPECT scan – variation in the metabolism of Tumors cells and normal brain tissue • Myelography • Biopsy
  • 13. Supportive Measures to reduce ICP • Head elevation • Hyperventilation • Hypothermia • Osmotic diuretics – 20% mannitol 0.25g/kg
  • 14. • Corticosteroids – 0.1 to 0.2mg/kg 6th hrly • Acetazolamide & frusemide - Anticonvulsive drugs – phenobarbitone - Shunting procedures for Hydrocephalus
  • 15. Specific • Surgery - Primary modality of treatment - Good prognosis if complete surgical removal is possible. Pilocytic Astrocytoma, Choroid plexus papilloma - Not possible in pontine glioma, Germ cell tumors and pineal tumors
  • 16. • Radiotherapy: - Tumor cannot be removed surgically - Residual tumor - Craniospinal irradiation – Medulloblastoma, Ependymoma,Germ Cell tumors, Pineoblastoma - Avoid <4yrs
  • 17. • Chemotherapy: - Adjuvant therapy to surgery - In children <4yrs to delay radiotherapy - Some chemosensitive tumors – Pineal tumors, Medulloblastoma, ependymoma, Astrocytoma
  • 18. Newer techniques • Steriotactic radiosurgery • Intensity modulated radiation therapy • Gene therapy – high grade gliomas • High dose chemotherapy
  • 19. • Growth factor inhibitors • Angiogenesis inhibitors • Radiosensitizers • Immunotherapy
  • 20. PROGNOSIS • Size and location of the tumor • Grade of tumor • Age of child • Metastasis at diagnosis • Residual tumors
  • 21. Name & location of cells Survival Rates Treatment Medulloblastoma (cerebellum) 50 percent after five years Surgery, radiation, chemotherapy, clinical trials. Recurrent cancer: Stem cell transplant. Cerebellar astrocytoma (cerebellum) 90 percent after five years Surgery, radiation after repeat surgical procedures. Recurrent cancer: Surgery first, then radiation, chemotherapy only if surgery and radiation are not working, clinical trials. Infratentorial ependymoma (fourth ventricle and spinal cord cavity) 50 percent after five years Surgery and radiation following, possible use of chemotherapy for young children. Recurrent cancer: Poor response to surgery and radiotherapy, cisplatin chemotherapy works for one third of patients, clinical trails should be considered. Brain stem glioma (brain stem) Most patients die in 18 months Usually cannot be surgically removed; use radiation, not chemotherapy except for children under three to delay radiation. Recurrent cancer: No surgery, no chemotherapy and no radiation, maximum has already been administered. Clinical drug trials are only option.
  • 22. Name & location of cells Survival Rates Treatment Cerebral astrocytoma, low grade (cerebrum) Over 80 percent after five years Surgery, radiation and chemotherapy only if not surgically removed. Recurrent cancer: Chemotherapy after maximum surgery and radiation, clinical trials. Cerebral astrocytoma, high grade (cerebrum) 20-50 percent after five years Surgery, radiation and chemotherapy. Chemotherapy is used for children under three to delay radiation. Recurrent cancer: Chemotherapy after radiation, clinical trials. Supratentorial ependymoma (back of the brain and adjacent ventricles) 50 percent after five years Surgery followed by radiation. Chemotherapy to delay radiation for very young children. Recurrent cancer: Seldom controlled after surgery and radiation. Cisplatin chemotherapy works for one-third of patients. Clinical trails should be considered. Craniopharyngioma (benign tumors in the central brain tissue) Unknown Surgery is usually successful. Recurrent cancer: Radiation.
  • 23. Name & location of cells Survival Rates Treatment Intracranial germ cell tumor Variable No surgery. Chemotherapy and radiation. Recurrent cancer: Chemotherapy, clinical trials. Recurrent cancer: Chemotherapy, clinical trials. Pineal tumors (pineal gland, undifferentiated cells) 50 percent after five years Radiation and chemotherapy. Surgery is not possible. Chemotherapy to delay radiation for very young children. Optic tract glioma (optic nerves, create visual symptoms) Unknown For younger children: chemotherapy, then radiation if chemo fails. Radiation earlier for older children. Observation.