Seminars in bone pathology. Conventional osteosarcoma. Present advances. What is new and what is old?
- Authors: Rogozhin D.V.1, Boulytcheva I.V.2, Kushlinskiy N.E.3, Soloviev Y.N.3, Bertoni F.4, Bacchini P.4, Kazakova A.N.1
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Affiliations:
- Russian Children’s Clinical Hospital
- FSBI Polyclinic No. 1 of the Business Administration for the President of the Russian Federation
- N.N Blokhin Russian Cancer Research Center
- Rizzoli Orthopaedic Institute, Bologna, Via Giulio Cesare Pupilli, 1
- Issue: Vol 6, No 2 (2014)
- Pages: 9-18
- Section: BONE SARCOMAS
- Published: 26.06.2014
- URL: https://sarbon.abvpress.ru/jour/article/view/464
- ID: 464
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Abstract
Osteosarcoma (OS) is the most common primary malignant bone tumor of connective tissue origin it affects teenagers in a very aggressive way. It causes significant harm with poor prognosis, and it is very difficult to cure. during the past two decades, the emergence of neoadjuvant chemotherapy of osteosarcoma has greatly improved the survival rate of osteosarcoma patients (5 year survival 60–70%). nearly half of these patients are not sensitive to chemotherapy drugs and die due to lung metastasis within 2 to 3 years.
The majority of patients (80%) have small tumor foci transferred into their systemic blood before treatment; the importance of improving long-term survival in patients by controlling lung metastases through effective drug and gene regulation has been increasingly recognized. the invasive ability of tumor cells is one of the important factors in their capacity to metastasize to distant locations in the body. Production of woven bone by tumor cells defines the neoplasm, however, variable amounts of cartilage and fibrous tissue matrix are often encountered as accompanying components. Osteoblastic, chondroblastic and fibroblastic types comprise the 3 major cell types of OS, but the percentage of cell type and matrix will vary in any individual case. The role of the pathologist is becoming more important because of the modern genetic and molecular and IHC markers in diagnostic procedures, the pathologists must rise to the occasion.
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About the authors
D. V. Rogozhin
Russian Children’s Clinical Hospital
Moscow
Russian FederationI. V. Boulytcheva
FSBI Polyclinic No. 1 of the Business Administration for the President of the Russian Federation
Author for correspondence.
Email: irena@boulytcheva.com
Moscow
Russian FederationN. E. Kushlinskiy
N.N Blokhin Russian Cancer Research Center
Moscow
Russian FederationYu. N. Soloviev
N.N Blokhin Russian Cancer Research Center
Moscow
Russian FederationF. Bertoni
Rizzoli Orthopaedic Institute, Bologna, Via Giulio Cesare Pupilli, 1
Bologna
ItalyP. Bacchini
Rizzoli Orthopaedic Institute, Bologna, Via Giulio Cesare Pupilli, 1
Bologna
ItalyA. N. Kazakova
Russian Children’s Clinical Hospital
Moscow
Russian FederationReferences
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