CC BY-NC-ND 4.0 · South Asian J Cancer 2016; 05(03): 138-145
DOI: 10.4103/2278-330X.187587
Review Article

Indian data on bone and soft tissue sarcomas: A summary of published study results

Anant Ramaswamy
Department of Medical Oncology, Tata Memorial Hospital, Mumbai, Maharashtra
,
Bharat Rekhi
Department of Pathology, Tata Memorial Hospital, Parel, Mumbai, Maharashtra
,
Sameer Bakhshi
All India Institute of Medical Sciences, New Delhi
,
Sachin Hingmire
Department of Oncology, Deenanath Mangeshkar Hospital, Pune, Maharashtra
,
Manish Agarwal
Department of Orthopedic Oncology, P. D. Hinduja Hospital and Medical Research Centre, Mumbai, Maharashtra
› Author Affiliations
Financial support and sponsorship: Nil.

Abstract

Bone sarcomas are rare tumors, approximating 0.2% of all cancers, with osteosarcoma (OGS), chondrosarcoma, and Ewing sarcoma being the most common cancers in this subset. The formation of disease management groups/clinics focused on sarcomas has resulted in better understanding and management of these uncommon tumors. Multiple large-scale retrospective data from Tata Memorial Hospital (TMH) and All India Institute of Medical Sciences have reported outcomes comparable to Western data in the field of OGS and Ewing sarcoma, with interesting prognostic factors identified for further evaluation. Soft tissue sarcomas are a rare heterogeneous group of tumors, more than 50 different tumor entities. The common subtypes identified in India include Ewing sarcoma and synovial sarcoma. Valuable work regarding brachytherapy has been done by radiation oncologists from the TMH, especially in pediatric patients.



Publication History

Article published online:
28 December 2020

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