An Overview of Glial Tumours

 Introduction

Tata Memorial Hospital Neuro-Oncology data 2006

Etiology

Classification

Clinical Features

Imaging

Immuno-cytochemistry

Staging & Grading

Natural History of Astrocytomas

Prognostication

Oligodendroglioma

Ependymoma

Prognosis

Supportive Treatment

 

Principles of Supportive treatment :

Supportive treatment has a significant role in brain tumour.

Agents used in supportive management of brain tumour -

§ Corticosteroids

- Dexamethasone

- Solumedrol

§ Anticonvulsants

- Phenetoin

- Valproic acid

- Phenobarbitone

- Carbapamazipine

§ Anti-coagulants / IVC filter

Description of agents -

Corticosteroid :

Acts by :

1) Anti-oedema effect – by reducing capillary permeability.

2) Tumorcidal effect – by increasing apoptosis.

Dexamethasone used with minimal dosage (4-8 mg/d).Max. dose = 100mg /day

Dexamethasone is used in brain tumor for following reasons -

1. Crosses Blood Brain Barrier

2. Little mineralo-corticoid activity

3. Lower probability of infection

4. Lower cognitive dysfunction

§ Symptoms improve by 24-72 hr.

§ Headache responds better than focal-deficit.

§ But, imaging need >7 day for to show response

Side-effects

1. Fluid retention , wt gain

2. Myopathy, gastritis , hyperglycemia

3. Infection (pneumocystis carinii )

Co-trimoxazole prophylaxis used to prevent infection

Indications :

1. Symptomatic brain metastasis

2. During Radiotherapy, if volume of treatment is large.

3. Post surgery – usually < 4 week.

4. Sign of increased intracranial tension.

Always used in minimal dose and least duration to prevent complication.

Anticonvulsant :

§ Seizure is the presenting symptom in 10-20% and occurs during disease progression in another 15-20%. Thus, 25-50% patient have episodes of convulsion. Rest 45% patient never has convulsive episodes.

§ If presents with seizure; treated with anticonvulsant (phenytoin). EEG may be done for confirmation.

§ Role of anticonvulsant as prophylactic is doubtful.

§ Brain tumour pts do have problem with anticonvulsants. Anticonvulsant should be used routinely or not is a matter of debate.

Those who prefer anti-convulsant at the earliest, arguments are

1. Epileptogenic foci always present.

2. May precipitate convulsion any time.

And those who are against routine use of anti-convulsant, arguments are

1. 50-55% never have convulsion.

2. Treatment of cause necessary to prevent convulsion.

3. Interfere with Chemotherapy / steroid.

4. More complications.

Use of routine anticonvulsant in brain tumor are not without problem :

1. More drug rash (20%) – morbilliform rash, steven-johnson reaction, shoulder hand syndrome.

2. Induces hepatic metabolism of steroid.

3. Reduces blood concentration of chemotheraputic agents.

4. Chemotheraputic agents may reduce phenytoin level & precipitate break-through siezure.

Indications of anticonvulsant:

1. Patient with seizure episodes or high risk for seizure episodes.

2. No definite role of prophylactic anti-convulsants.

Except in few situations, like –

§ Lesion in highly epileptogenic area ( motor cortex)

§ Both brain parenchymal & leptomeningeal disease.

§ Multiple brain metastasis.

§ No proper follow up and no immediate treatment facility in case of convulsive episodes.

 

More information soon …….

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Brain Tumour Foundation Of India
189 B, 1 st Floor, Golden Jubilee Block, 

Tata Memorial Hospital, Ernest Borges Marg, Parel, Mumbai - 400 012, INDIA
Tel : 91-22-2417 7000, Ext : 4559. Fax : 022-2417 7159 / 2414 6937
Email : btf@braintumourindia.com