Synovial sarcoma

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Synovial sarcoma Microchapters

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Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Synovial sarcoma from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

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Case #1

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Treatment

Treatment usually involves:

  • Surgery, to remove the tumor and a safety margin of healthy tissue. This is the mainstay of synovial sarcoma treatment and is curative in approximately 20-70% of patients, depending on the particular study being quoted.
  • Conventional chemotherapy, (for example, Doxorubicin hydrochloride and Ifosfamide), to reduce the number of remaining microscopic cancer cells. The benefit of chemotherapy in synovial sarcoma to overall survival remains unclear, although a recent study has shown that survival of patients with advanced, poorly differentiated disease marginally improves with doxorubicin/ifosfamide treatment.
  • Radiotherapy to reduce the chance of local recurrence. The benefit of radiotherapy in this disease is less clear than for chemotherapy.

Recent laboratory-based studies have identified a number of potential systemic therapies that may prove more effecacious than conventional chemotherapy and improve survival, however the rarity of this tumor makes clinical trial organization difficult and validation of these experimental therapeutics will likely be long in coming.

Scans to be undertaken before, during, and after treatment

Various scanning techniques can be used to further localise and identify this cancer:

During treatment, the patient may have Bone Density Scans, to measure the impact of the chemotherapy on the skeleton.

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