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  • Chilhood Osteosarcoma

Childhood Osteosarcoma Treatment | I D Cancer Center Lucknow

What Is Childhood Osteosarcoma?

Osteosarcoma develops when immature bone-forming cells (osteoblasts) grow uncontrollably and form tumors. These tumors:

  • Commonly occur during growth spurts

  • Often affect children aged 10–18 years

  • May spread (metastasize) to the lungs or other bones if not treated early


Common Symptoms of Osteosarcoma

Parents should watch for:

  • Persistent bone pain, often worse at night

  • Swelling or a noticeable lump around a bone or joint

  • Difficulty moving the affected limb

  • Limping (if leg involved)

  • Sudden fractures with minimal injury

  • Warmth or redness over the affected area

Any persistent bone pain in a child should not be ignored.


Risk Factors

While most cases occur without a clear cause, risk factors include:

  • Rapid bone growth during puberty

  • Previous radiation therapy

  • Certain genetic conditions (Li-Fraumeni syndrome, retinoblastoma gene mutation)

  • Family history of rare cancers


How Childhood Osteosarcoma Is Diagnosed

At I D Cancer Center, diagnosis follows a systematic, child-friendly approach:

1. Clinical Examination

Assessing pain, swelling, mobility, and function.

2. Imaging

  • X-ray (initial detection)

  • MRI (best for local extent and surgical planning)

  • CT scan chest (check lung spread)

  • PET-CT for whole-body evaluation

  • Bone scan (selected cases)

3. Biopsy

A core needle biopsy or surgical biopsy confirms the diagnosis and tumor type.

4. Pathology & Molecular Testing

  • Determines tumor grade

  • Helps identify aggressive features

  • Guides treatment decisions

5. Baseline Blood Tests

Includes CBC, renal/liver profile, and alkaline phosphatase levels.


Treatment Options at I D Cancer Center

Childhood osteosarcoma requires coordinated multidisciplinary care.

1. Chemotherapy

Used before and after surgery:

  • Preoperative chemotherapy reduces tumor size

  • Postoperative chemotherapy eliminates remaining cancer cells

2. Surgery

Goal: Complete removal of tumor while preserving function

  • Limb-sparing surgery (preferred)

  • Endoprosthetic reconstruction

  • Rotationplasty (selected cases)

  • Amputation (rare, only when necessary)

We collaborate with specialized pediatric orthopedic surgeons.

3. Radiation Therapy

Used when:

  • Surgery is not possible

  • Margins are positive

  • Palliation is needed

Advanced techniques at I D Cancer Center:

  • IMRT / VMAT

  • IGRT daily image guidance

  • SBRT for selected metastasis

  • Lung-directed radiotherapy (for metastatic nodules)

4. Targeted & Immunotherapy

Used in:

  • Relapsed cases

  • Tumors with specific molecular markers

5. Supportive Care

Essential throughout therapy:

  • Pain management

  • Physiotherapy and limb rehabilitation

  • Infection control

  • Nutrition support

  • Emotional counseling for the child and family

6. Long-Term Follow-Up

To monitor:

  • Limb function

  • Growth and development

  • Lung health

  • Treatment-related side effects


Prognosis

Prognosis depends on:

  • Tumor size and location

  • Metastasis at diagnosis

  • Response to preoperative chemotherapy

  • Ability to achieve complete surgical removal

With modern therapies, many children achieve long-term survival and return to normal activities.