Bone Tumors Saurabh Agrawal Multidisciplinary team approach… Factors to consider Type Size Stage Age BENIGN INTERMEDIATE MALIGNANT
Latent – no treatment Grading & staging
unless symptomatic Locally aggressive – frequent Surgical resection Active – biopsy & recurrence; may with other modalities curettage as required en bloc require Limited capacity for resection recurrence but if Close follow-up occurs it is non- destructive Surgery For primary operable tumours, the options are tumor excision withlimb salvage , oramputations . For locally advanced lesions amputation may be considered Resection with clean margins (pseudocapsule and cuff of normal tissue) Margin of resection – as per local staging imaging, closest critical structure (e.g., neurovascular bundle) Limb salvage can be challenging in the skeletally immature because resection requires excision of the physes, particularly those around the knee, with subsequent implications for limb length discrepancy (Benign & intermediate) Reconstruct… endoprosthetic replacement allograft-prosthetic composite allograft using donated bone extracorporeal sterilization and reimplantation of the patient’s own bone vascularized and non-vascularized autograft arthrodesis Neoadjuvant and Adjuvant therapies To reduce the size of large tumors prior to surgery To treat micrometastases by systemic chemotherapy Local control using radiation therapy Benign lesions Osteochondroma Enchondroma Osteoid Giant cell tumor osteoma (osteoclastoma) Treatmen Benign – excision Usually no treatment CT-guided extended intralesional t Malignant – wide required but radiofrequency curettage with a detailed excision or curettage can be ablation debridement of the lesion amputation done if it is painful or wall + use of adjuvants like causes pathological phenol, bone cement, liquid # nitrogen Excision with reconstruction Amputation Radiotherapy - spine Osteosarcoma Chemotherapy Multiagent chemotherapy with doxorubicin, cisplatin, high dose methotrexate, isofosfamide and etoposide for minimum 3 cycles prior to local control by surgery. Supportive care to manage the s/e of the drugs
*Since OS is radioresistant so radiotherapy is not used commonly in
management Ewing’s sarcoma Radiation sensitive tumour Radiotherapy, in combination with chemotherapy can achieve local control but definitive surgery when feasible has to be regarded as the first choice of local therapy Definitive RT - if complete surgery is not feasible e.g., spine, skull, pelvis, head and neck, thorax; 55-60 Gy in 28-30 fractions over 5-7 weeks Postop RT - gross residual disease or positive surgical margins or poor histological response in the surgical specimen (i.e.>10% viable tumour cells); 45-50.4 Gy in 25-28 fractions over 5-6 weeks Palliative RT - incurable or metastatic disease for alleviation of local symptoms like pain, bleeding, fungation or metastatic symptoms like dyspnoea, spinal cord compression, brain metastases etc. Chemotherapy Multiagent therapy preferred with doxorubicin, cyclophosphamide, ifosfamide, vincristine, dactinomycin, and etoposide Total duration is 48 weeks Supportive care to manage the s/e of the drugs Metastatic bone disease Most common malignancy of bone Most common primary tumours to metastasize to bone Males – prostate carcinoma Females – breast carcinoma Children – adrenal neuroblastoma Other – lungs, renal and thyroid carcinomas Common sites (in order of frequency) – thoracic spine, proximal femur, pelvis, proximal humerus, scapula, distal femur and ribs C/F - pain, swelling, abdominal mass, pathological fracture, spinal cord compression and hypercalcaemia X-ray appearance – blastic/sclerotic – prostate lytic – kidney, thyroid, lung mixed – breast Biopsy – solitary bone lesion, no known primary cancer, a long disease-free interval following a previous malignancy, or history of more than one previous invasive cancer Management Analgesia Hormonal therapy, bisphosphonates, chemotherapy, radiotherapy Bisphosphonates are useful in metastatic breast and prostate carcinoma and multiple myeloma Surgery for intractable pain, or impending or pathological fractures THANK YOU References Apley and Solomon’s System of Orthopaedics and Trauma, 10e (2018) ICMR. Consensus Document for Management of Soft Tissue Sarcoma and Osteosarcoma (2016) Essential Orthopaedics, 5e (2015)