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Soft tissue sarcoma (STS) is a type of cancer that begins in the soft tissues like fat, muscles, nerves, blood vessels, tendons, and connective tissues. It can occur anywhere in the body.
• 60% – Found in arms or legs.
• 30% – Found in the torso or abdomen.
• 10% – Found in the head and neck.
• Though it affects people of all ages, it is more common in children.
• Blood vessels
• Fat cells
• Joint linings
• Muscles
• Nerves
• Tendons
There are over 70 different types of STS, each named after the type of cell or tissue from which it originates.
• In 2023, 13,400 new STS cases are expected to be diagnosed in the United States.
• The 5-year survival rate for STS in the United States is approximately 65%.
Although the exact cause of many sarcomas remains unknown, several risk factors increase the chances of developing STS:
1. Previous Radiation Therapy:
• People who underwent radiation therapy over five years ago are at higher risk of developing sarcoma at the treatment site.
2. Genetic Disorders:
• Conditions like neurofibromatosis type 1, Li-Fraumeni syndrome, retinoblastoma, Werner syndrome, and familial adenomatous polyposis increase the risk of sarcoma.
3. Weakened Immune System:
• Individuals with HIV/AIDS, leukemia, lupus, or other autoimmune disorders.
4. Lymphedema:
• Swelling in limbs or other areas following surgery or radiation therapy may lead to angiosarcoma.
5. Exposure to Chemicals:
• Long-term exposure to certain industrial chemicals increases the risk.
Symptoms depend on the location of the sarcoma:
• Painless lump or swelling in the arm or leg.
• Pain may develop as the tumor grows and presses on nerves or muscles.
• Lumps larger than 2 inches (5 cm) or those that cause pain should be evaluated by a doctor.
• Abdominal sarcomas may cause bleeding or abdominal swelling.
• Uterine sarcomas may lead to abnormal bleeding or enlargement of the uterus.
• X-ray
• Ultrasound
• CT Scan
• MRI
• PET-CT
• Biopsy: A small tissue sample is taken and analyzed under a microscope to confirm cancer.
• Types of biopsy: Needle biopsy, incisional biopsy, excisional biopsy.
1. Surgery
• Surgery removes the tumor along with a margin of healthy tissue.
• For low-grade tumors, surgery alone may be sufficient.
• For high-grade tumors larger than 2 inches, a combination of surgery and radiation therapy or chemotherapy is often used.
• In some cases, amputation may be required to remove large tumors involving critical nerves and blood vessels.
2. Radiation Therapy
• High-energy radiation destroys cancer cells.
• Radiation can shrink tumors before surgery (neoadjuvant) or eliminate remaining cancer cells after surgery (adjuvant).
• External Beam Radiation Therapy (EBRT) is the most common type.
• IMRT and SBRT techniques focus radiation precisely, minimizing damage to surrounding tissues.
• Side effects include fatigue, skin redness, itching, and swelling.
3. Chemotherapy
• Chemotherapy uses drugs to kill cancer cells. It is usually given in cycles.
• Common drugs for STS include:
• Doxorubicin
• Ifosfamide
• Gemcitabine
• Docetaxel
• Paclitaxel
• Side effects may include fatigue, nausea, vomiting, hair loss, infections, and diarrhea.
4. Targeted Therapy
• Targets specific genes and proteins involved in the growth of cancer.
• Common targeted therapy drugs:
• Imatinib (Gleevec)
• Pazopanib (Votrient)
• Tazemetostat (Tazverik)
• Pexidartinib (Turalio)
5. Immunotherapy
• Boosts the body’s immune system to fight cancer cells.
• Immunotherapy drugs for STS:
• Atezolizumab (Tecentriq)
• Tumor-agnostic treatments.
• Regular follow-ups are essential to monitor for recurrence and manage side effects.
• Follow-ups may include:
• Physical exams
• Blood tests
• Imaging tests like X-rays, CT scans, or MRIs.
STS can be challenging to treat, but early detection and timely intervention significantly improve outcomes. Continuous follow-ups ensure that patients remain healthy and catch any recurrence at the earliest stage.
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