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Sarcoma and Bone Cancers

Our Cancer Specialties

Breast Cancer
Head & Neck Cancer
Gastrointestinal
Lung Cancer
Gynecologic Cancer
Urologic Cancer
Thyroid & Endocrine Cancer
Bone & Sarcoma Cancer
Skin Cancer
Pediatric Cancer
Rare Cancers

    Soft Tissue and Bone sarcoma Hospital in Banjara Hills, Hyderabad

    Sarcomas are rare cancers arising from bone, muscle, fat, blood vessels, or connective tissues. Because they are uncommon and often misdiagnosed as benign swellings, early specialist evaluation is critical. Our sarcoma care is centralized, protocol-driven, and tumor-board discussed. We focus on limb preservation, precision pathology, molecular profiling, and access to modern systemic therapies

    What is Sarcoma?

    Sarcomas are rare, complex cancers originating in the bones or soft tissues. Soft tissue sarcomas can arise in limbs, trunk or in abdomen commonly as retro peritoneal sarcomas.We provide protocol-driven care through a dedicated multidisciplinary team focused on precision and patient outcomes. Unlike common cancers, sarcomas require highly specialized knowledge for accurate diagnosis and effective limb-sparing treatments.

    Bone Cancers

    Osteosarcoma, Ewing Sarcoma, Chondrosarcoma.

    Symptoms to Monitor
    Persistent Bone Pain
    Sometimes with fever
    Swelling near joints
    Unexplained fracture
    Limping in children or adolescents
    Diagnosis at HCC
    MRI-based local staging
    PET CT scan
    CT chest for metastasis
    Core needle biopsy (planned along surgical incision line)
    Molecular testing (EWSR1 translocation in Ewing sarcoma)
    Diagnosis at HCC
    Neoadjuvant chemotherapy (standard osteosarcoma protocols)
    Endoprosthetic reconstruction
    Adjuvant chemotherapy
    Radiation therapy (Ewing sarcoma)
    Soft Tissue Sarcomas
    Liposarcoma
    Leiomyosarcoma
    Synovial sarcoma
    Undifferentiated pleomorphic sarcoma
    GIST (managed under GI oncology protocol)
    Sarcoma and Bone Cancers

    Treatment Approach at HCC

    Surgical Oncology

    Wide local excision with negative margins
    Limb preservation wherever possible
    Complex retroperitoneal resections

    Radiation Therapy

    Pre-operative radiation to shrink tumor
    IMRT / image-guided radiation
    Proton therapy referral where indicated

    Systemic Therapy

    Doxorubicin-based chemotherapy
    Ifosfamide combinations
    Eribulin (liposarcoma)
    Pazopanib (advanced soft tissue sarcoma)

    Precision & Immunotherapy

    Pembrolizumab in selected subtypes
    NTRK inhibitors in fusion-positive sarcomas
    CDK4 amplification targeting in specific liposarcomas
    MDM2 amplification testing

    Pediatric & Young Adult Sarcomas

    Sarcomas commonly affect children and adolescents. Treatment is protocol-driven and coordinated with pediatric oncology specialists. Fertility preservation counselling is offered before chemotherapy where appropriate.

    Genetic & Hereditary Evaluation

    Certain sarcomas are linked with inherited conditions: Li-Fraumeni syndrome (TP53 mutation), Neurofibromatosis type 1, Retinoblastoma mutation carriers. Genetic counselling and family screening are offered when indicated.

    FAQ’s

    Reviewed By

    Medically Reviewed by : Dr. Srinivas Prasad, MCh (Surgical Oncology)
    20+ years of experience in oncologic surgery and multidisciplinary cancer care.
    Registration No: 2111
    Last reviewed: February 2026