What Patients Should Know About Sarcoma and Immunotherapy

Sarcoma is rare and complex. Immunotherapy isn’t yet an option for everyone — but it’s changing what’s possible for some patients, and research is rapidly expanding those possibilities.

A sarcoma diagnosis can bring uncertainty, fear, and a lot of questions. Because sarcoma is rare, finding clear, reliable information can sometimes feel just as challenging as navigating treatment itself.

While surgery, chemotherapy, and radiation remain the backbone of treatment for many sarcomas, immunotherapy is creating new possibilities for some patients. Researchers are working to expand those options to more people. This Sarcoma Awareness Month, here’s what you should know about sarcoma, immunotherapy, and where the field is headed.


Sarcoma is a rare group of cancers that develops in connective and supportive tissues throughout the body, including bone, muscle, fat, cartilage, blood vessels, and tendons. Unlike more common cancers that begin in organs such as the breast, lung, or colon, sarcomas can arise almost anywhere in the body.

There are more than 70 recognized types of sarcoma, which are broadly divided into soft-tissue and bone sarcomas. Each type behaves differently and may respond differently to treatment, making an accurate diagnosis especially important.

Some prominent sarcomas include:

  • osteosarcoma, which resembles bone
  • chondrosarcoma, which resembles cartilage
  • liposarcoma, which resembles fat
  • leiomyosarcoma, which closely resembles smooth muscle

The exact cause of most sarcomas is unknown. However, several factors can increase a person’s risk, including:

  • Previous radiation therapy
  • Exposure to certain chemicals
  • Long-term swelling caused by damage to the lymphatic system (lymphedema)
  • Infection with human herpesvirus 8, which is associated with Kaposi sarcoma
  • Certain hereditary conditions, including Li-Fraumeni syndrome, hereditary retinoblastoma, neurofibromatosis type 1, and familial adenomatous polyposis (FAP)

Because many sarcomas develop deep within muscles or other tissues, they may not cause symptoms until they have grown quite large. That’s why any new lump — particularly one that is growing, painful, or larger than a golf ball — should be evaluated by a healthcare provider. While most lumps are not cancer, early evaluation is important.

Treatment depends on the specific type, location, and stage of the disease. Surgery is often the primary treatment when the tumor can be safely removed, while chemotherapy and radiation therapy may be used before or after surgery or to treat more advanced disease. Unfortunately, some sarcomas do not respond well to these treatments, highlighting the need for new approaches like immunotherapy.


Immunotherapy is a type of cancer treatment that helps your immune system recognize and attack cancer. Normally, the immune system can detect and destroy abnormal cells, but cancer can develop ways to hide from immune attack or switch it off entirely. Immunotherapy helps remove these barriers, allowing the immune system to better recognize and fight cancer.

Immunotherapy has transformed treatment for several types of cancer, but sarcoma presents unique challenges. Because sarcoma includes dozens of distinct diseases, treatments that work well for one subtype may have little effect in another. As a result, immunotherapy is currently approved only for certain sarcoma subtypes or tumors with specific genetic features.

  • Immune Checkpoint Inhibitors (ICIs) – treatments that help the immune system better recognize and attack cancer by releasing the “brakes”:
    • Atezolizumab (Tecentriq®): Approved for alveolar soft part sarcoma (ASPS), a rare subtype
    • Pembrolizumab (Keytruda®): Approved for sarcomas with specific biomarkers
    • Dostarlimab (Jemperli®): Approved for sarcomas with specific biomarkers
  • Engineered T-cell (TCR) therapy – T-cell therapy takes a patient’s own T cells and modifies them in a lab so that they can recognize cancer cells, before infusing them back into the patient. One TCR is approved for sarcoma, and it is the first engineered TCR approved for a solid tumor:
    • Afamitresgene autoleucel (Tecelra®): Approved for certain cases of synovial sarcoma, a rare form of soft tissue sarcoma

It’s important to talk to your healthcare provider to determine if immunotherapy would benefit you or your loved ones.


In many ways, the story of cancer immunotherapy began with sarcoma.

More than a century ago, Dr. William B. Coley observed that some patients with sarcoma experienced tumor shrinkage after developing bacterial infections. He later developed “Coley’s toxins” to intentionally stimulate the immune system against cancer — work that is now recognized as one of the earliest foundations of modern cancer immunotherapy. His daughter would go on to use this work to co-found the Cancer Research Institute (CRI) in 1953.


Although today’s immunotherapies don’t yet benefit every person with sarcoma, researchers are making steady progress toward changing that.

Today, CRI-funded scientists are pursuing several approaches to improve immune-based treatments for sarcoma and other difficult-to-treat solid tumors.


A sarcoma diagnosis can feel overwhelming, but you don’t have to navigate it alone. Learning about your specific subtype, asking questions, and seeking care from specialists with experience treating sarcoma can help you make informed decisions about your treatment.

Don’t hesitate to ask about clinical trials, which may provide access to promising new therapies while helping advance research for future patients. And remember to lean on family, friends, healthcare providers, and patient advocacy organizations for support throughout your journey.


Sources

Cancer Stat Facts
National Cancer Institute, 2026

Sarcoma
Mayo Clinic, 2025

What is Sarcoma?
Sarcoma Foundation of America, 2026


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