Sarcoma
A sarcoma is a cancer that arises from transformed cells of mesenchymal origin. Connective tissue is a broad term that includes bone, cartilage, fat, vascular, or hematopoietic tissues, and sarcomas can arise in any of these types of tissues. As a result, there are many subtypes of sarcoma, which are classified based on the specific tissue and type of cell from which the tumor originates. Sarcomas are primary connective tissue tumors, meaning that they arise in connective tissues. This is in contrast to secondary connective tissue tumors, which occur when a cancer from elsewhere in the body spreads to the connective tissue. The word sarcoma is derived from the Greek σάρκωμα sarkōma "fleshy excrescence or substance", itself from sarx meaning "flesh".
Classification
Sarcomas are typically divided into two major groups: bone sarcomas and soft tissue sarcomas, each of which has multiple subtypes. In the United States, the American Joint Committee on Cancer publishes guidelines that classify the subtypes of sarcoma. These subtypes are as follows:Subtypes of bone sarcoma:
- Osteosarcoma
- Chondrosarcoma
- Poorly differentiated round/spindle cell tumors
- Hemangioendothelioma
- Angiosarcoma
- Fibrosarcoma/myofibrosarcoma
- Chordoma
- Adamantinoma
- Other:
- * Liposarcoma
- * Leiomyosarcoma
- * Malignant peripheral nerve sheath tumor
- * Rhabdomyosarcoma
- * Synovial sarcoma
- * Malignant solitary fibrous tumor.
- Liposarcoma
- Atypical lipomatous tumor
- Dermatofibrosarcoma protuberans
- Malignant solitary fibrous tumor
- Inflammatory myofibroblastic tumor
- Low-grade myofibroblastic sarcoma
- Fibrosarcoma
- Myxofibrosarcoma
- Low-grade fibromyxoid sarcoma
- Giant cell tumor of soft tissues
- Leiomyosarcoma
- Malignant glomus tumor
- Rhabdomyosarcoma
- Hemangioendothelioma
- Angiosarcoma of soft tissue
- Extraskeletal osteosarcoma
- Gastrointestinal stromal tumor, malignant
- Malignant peripheral nerve sheath tumor
- Malignant Triton tumor
- Malignant granular cell tumor
- Malignant ossifying fibromyxoid tumor
- Stromal sarcoma not otherwise specified
- Myoepithelial carcinoma
- Malignant phosphaturic mesenchymal tumor
- Synovial sarcoma
- Epithelioid sarcoma
- Alveolar soft part sarcoma
- Clear cell sarcoma of soft tissue
- Extraskeletal myxoid chondrosarcoma
- Extraskeletal Ewing sarcoma
- Desmoplastic small round cell tumor
- Extrarenal rhabdoid tumor
- Perivascular epithelioid cell tumor, not otherwise specified
- Intimal sarcoma
- Undifferentiated spindle cell sarcoma
- Undifferentiated pleomorphic sarcoma
- Undifferentiated round cell sarcoma
- Undifferentiated epithelioid sarcoma
- Undifferentiated sarcoma, not otherwise specified.
Signs and symptoms
Cause
Causes and risk factors
The cause of most bone sarcomas is not known, but several factors are associated with an increased risk of developing bone sarcoma. Previous exposure to ionizing radiation is one such risk factor. Exposure to alkylating agents, such as those found in certain cancer chemotherapeutic medicines, also increases the risk of bone sarcoma. Certain inherited genetic syndromes, including Li-Fraumeni syndrome, heritable RB1 gene mutations, and Paget's disease of bone, are associated with an increased risk of developing bone sarcomas.Most soft tissue sarcomas arise from what doctors call "sporadic" genetic mutations within an affected person's cells. Nevertheless, there are certain risk factors associated with an increased risk of developing soft tissue sarcoma. Previous exposure to ionizing radiation is one such risk factor. Exposure to vinyl chloride, arsenic and thorotrast all are associated with an increased risk of angiosarcoma. Lymphedema, such as that resulting from certain types of breast cancer treatment, also is a risk factor for development of angiosarcoma. As with bone sarcomas, certain inherited genetic syndromes also are associated with an increased risk of developing soft tissue sarcoma, including Li-Fraumeni syndrome, familial adenomatous polyposis, neurofibromatosis type 1, and heritable RB1 gene mutations.
Mechanisms
The mechanisms by which healthy cells transform into cancer cells are described in detail elsewhere. The precise molecular changes that result in sarcoma are not always known, but certain types of sarcomas are associated with particular genetic mutations. Examples include:- Most cases of Ewing sarcoma are associated with a chromosomal translocation in which part of chromosome 11 fuses with part of chromosome 22. This results in the EWS gene becoming fused to other genes, including the FLI1 gene in 90% of Ewing cases and ERG gene in 5-10% of cases. These fusions result in the production of abnormal proteins, although how these abnormal proteins result in cancer is not fully known.
- Dermatofibrosarcoma protuberans often is associated with a chromosomal translocation in which the COL1A1 gene becomes fused to the PDGFRB gene. This results in over-active PDGF signaling, which is thought to promote cell division and ultimately lead to tumor development.
- Inflammatory myofibroblastic tumor often is associated with rearrangements of the ALK gene, and occasionally with rearrangements of the HMGA2 gene.
- Giant cell tumor of soft tissue frequently is associated with a chromosomal translocation between chromosome 1 and chromosome 2, in which the CSF1 gene becomes fused with the COL6A3 gene. This results in increased CSF1 protein production, which is thought to play a role in cancer development.
- Many liposarcomas are associated with duplication of part of chromosome 12, which results in extra copies of known cancer-promoting genes such as the CDK4 gene, the MDM2 gene and the HMGA2 gene.
Diagnosis
Bone sarcomas
Diagnosis of bone sarcomas begins with a thorough history and physical examination which may reveal characteristic signs and symptoms. Laboratory studies are not particularly useful in diagnosis, although some bone sarcomas may be associated with elevated alkaline phosphatase levels, while others can be associated with elevated erythrocyte sedimentation rate. Importantly, however, none of these laboratory findings are specific to bone sarcomas, meaning that elevations in these lab values are associated with many other conditions as well as sarcoma, and thus cannot be relied upon to conclusively diagnose sarcoma. Imaging studies are critically important in diagnosis, and most clinicians will order a plain radiograph initially. Other imaging studies commonly used in diagnosis include magnetic resonance imaging studies and radioisotope bone scans. Computed tomography imaging typically is not used in diagnosis of most types of bone sarcoma, although it is an important tool for staging. Definitive diagnosis requires biopsy of the tumor and careful review of the biopsy specimen by an experienced pathologist.Soft tissue sarcomas
Diagnosis of soft tissue sarcomas also begins with a thorough history and physical examination. Imaging studies can include either CT or MRI, although CT tends to be preferred for soft tissue sarcomas located in the thorax, abdomen, or retroperitoneum. Positron emission tomography also may be useful in diagnosis, although its most common use is for staging. As with bone sarcomas, definitive diagnosis requires biopsy of the tumor with evaluation of histology by a trained pathologist.Staging
In general, cancer staging refers to how advanced a cancer is, and usually it is based upon factors such as tumor size and whether it has spread to other parts of the body. Staging is important because the stage affects the prognosis, as well as the types of treatments that are likely to be effective against the cancer. With sarcomas, staging requires a determination of whether the tumor has grown into surrounding tissues, as well as imaging to determine whether it has spread to lymph nodes or to other tissues or organs in the body.The most common imaging tools used for staging bone sarcomas are MRI or CT to evaluate the primary tumor, contrast-enhanced CT of the chest to evaluate whether the cancer has spread to the lungs, and radioisotope bone scan to evaluate whether the cancer has spread to other bones. Staging for soft tissue sarcomas typically includes imaging of the primary tumor by MRI or CT to determine tumor size, as well as contrast-enhanced CT of the chest to evaluate for metastatic tumors in the lungs.
Grade
Like some other cancers, sarcomas are assigned a grade based on the appearance of the tumor cells under a microscope. In general, grade refers to how aggressive the cancer is and how likely it is to spread to other parts of the body. Low-grade sarcomas have a better prognosis than higher-grade sarcomas, and are usually treated surgically, although sometimes radiation therapy or chemotherapy are used. Intermediate- and high-grade sarcomas are more frequently treated with a combination of surgery, chemotherapy, or radiation therapy. Since high-grade tumors are more likely to undergo metastasis, they are treated more aggressively. The recognition that many sarcomas are sensitive to chemotherapy has dramatically improved the survival of patients. For example, in the era before chemotherapy, long-term survival for pediatric patients with localized osteosarcoma was only about 20%, but now has risen to 60–70%.Prevention and screening
In the US, the US Preventive Services Task Force publishes guidelines recommending preventive screening for certain types of common cancers and other diseases. As of March 2019, the USPSTF does not recommend screening for sarcoma, possibly because it is a very rare type of cancer.The American Cancer Society also publishes guidelines recommending preventive screening for certain types of common cancers. Like the USPSTF, as of March 2019 ACS does not recommend preventive screening for sarcoma.
Treatment
is the most common form of the treatment for most sarcomas that have not spread to other parts of the body. Limb-sparing surgery, as opposed to amputation, can now be used to save the limbs of patients in at least 90% of extremity sarcoma cases. Additional treatments, including chemotherapy and radiation therapy, may be administered before surgery or after surgery. The use of neoadjuvant or adjuvant chemotherapy and radiotherapy significantly improves the prognosis for many sarcoma patients. Treatment can be a long and arduous process, lasting about a year for many patients.- Liposarcoma treatment consists of surgical resection, with chemotherapy not being used outside of the investigative setting. Adjuvant radiotherapy may also be used after surgical excision for liposarcoma.
- Rhabdomyosarcoma is treated with surgery, radiotherapy, or chemotherapy. The majority of rhabdomyosarcoma patients have a 50–85% survival rate.
- Osteosarcoma is a tumor of the bone that is treated with surgical resection of as much of the cancer as possible, often along with neoadjuvant chemotherapy. Radiotherapy is a second alternative although not as successful.
In childhood sarcomas, the cytotoxic agent cyclophosphamide is widely used and has shown good anti-tumour efficacy.
It is believed that higher doses of chemotherapy might improve survival. However, high doses of chemotherapy stop the production of blood cells in the bone marrow and can be harmful. Stem cells collected from people before high‐dose chemotherapy can be transplanted back to the person if the blood cell count gets too low; this is called autologous hematopoietic stem cell transplantation. Research to investigate if using high‐dose chemotherapy followed by autologous hematopoietic stem cell transplantation was more favourable then standard‐dose chemotherapy found only one RCT and this did not favour either of the two treatment arms with respect to overall survival. Further evidence is needed through well‐designed clinical trials.
Prognosis
Factors that affect prognosis
The AJCC has identified several factors that affect prognosis of bone sarcomas:- Size of the tumor: larger tumors tend to have a worse prognosis compared to smaller tumors.
- Spread of tumor to surrounding tissues: tumors that have spread locally to surrounding tissues tend to have a worse prognosis compared to tumors that have not spread beyond their place of origin.
- Stage and presence of metastases: tumors that have spread to the lymph nodes or other organs or tissues have a worse prognosis compared to tumors that have not metastasized.
- Tumor grade: higher grade tumors tend to have a worse prognosis compared to low grade tumors.
- Skeletal location: tumors originating in the spine or pelvic bones tend to have a worse prognosis compared to tumors originating in arm or leg bones.
- Stage: as with bone sarcomas, tumors that have metastasized have a worse prognosis compared to tumors that have not metastasized.
- Grade: the AJCC recommends using a grading system called the French Federation of Cancer Centers Sarcoma Group Grade for soft tissue sarcomas, with high-grade tumors having a worse prognosis compared to low-grade tumors.
- Mitotic rate: mitotic rate refers to the fraction of cells that are actively dividing within the tumor; GISTs that have a high mitotic rate have a worse prognosis compared to GISTs that have a low mitotic rate.
Outcome data
For soft tissue sarcomas, the overall 5-year survival is 64.5%, but survival is affected by many factors, including stage. Thus, the 5-year survival is 80.8% for soft tissue sarcomas that have not spread beyond the primary tumor, 58.0% for soft tissue sarcomas that have spread only to nearby lymph nodes, and 16.4% for soft tissue sarcomas that have spread to distant organs. The ACS estimates that 5,270 people will die from soft tissue sarcoma in 2019, accounting for 0.9% of all cancer deaths.
Epidemiology
Sarcomas are quite rare. The risk of a previously healthy person receiving a new diagnosis of bone cancer is less than 0.001%, while the risk of receiving a new diagnosis of soft tissue sarcoma is between 0.0014-0.005%. The American Cancer Society estimates that in the United States there will be 3,500 new cases of bone sarcoma in 2019, and 12,750 new cases of soft tissue sarcoma. Considering that the total estimated number of new cancer diagnoses is 1,762,450, this means bone sarcomas represent only 0.2% of all new cancer diagnoses and soft tissue sarcomas represent only 0.7% of all new cancer diagnoses in the US in 2019. These estimates are similar to previously reported data.Sarcomas affect people of all ages. Around 50% of bone sarcomas and 20% of soft-tissue sarcomas are diagnosed in people under the age of 35. Some sarcomas, such as leiomyosarcoma, chondrosarcoma, and gastrointestinal stromal tumor, are more common in adults than in children. Most high-grade bone sarcomas, including Ewing's sarcoma and osteosarcoma, are much more common in children and young adults.
In fossils
In 2016, scientists reported the discovery of an osteosarcoma tumor in a 1.6-1.8 million-year-old fossil from the skeleton of now-extinct hominin species, making it the earliest-known case of human cancer.Research
Treatment of sarcoma, especially when the sarcoma has spread, or "metastasized", often requires chemotherapy but existing chemotherapeutic medicines are associated with significant toxicities and are not highly effective in killing cancer cells. Therefore, research to identify new medications to treat sarcoma is being conducted. One possibility is the use of cancer immunotherapy to treat sarcomas. This is not yet an established treatment tool. Other strategies, such as small-molecule targeted therapy, biologic agents, and nanoparticle-directed therapy, also are being investigated.Research to understand the specific genetic and molecular factors that cause sarcoma to develop is underway. This could allow for the design of new targeted therapies and allow physicians to more accurately predict a patient's prognosis.
Presence of the H3-B3 immunoregulatory checkpoint receptor in the tumor cells provides the opportunity for clinical trial testing of new drugs and targeted agents and immunotherapies in development.