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obsolete non-metastatic fibrosarcoma
Description
Definition and Characteristics
Non-metastatic fibrosarcoma, also referred to as "obsolete" in some contexts, is a type of cancer that originates from the soft tissues. It is characterized by its slow growth rate and limited ability to spread to other parts of the body.
- According to source [8], the majority of these tumors do not metastasize, and no metastases occurred in their series.
- Fibrosarcomas are defined as malignant neoplasms composed of fibroblasts that may have varying amounts of collagen production and a "herringbone" architecture (source [11]).
Incidence and Survival Rates
The incidence of adult-type fibrosarcoma has been declining over the past several decades. The 5-year survival rate for this type of cancer is between 40% and 60%. Researchers are investigating new ways to slow its growth.
- Between 40% and 60% of people who have adult-type fibrosarcoma are alive five years after diagnosis (source [14]).
- The 10-year survival rate for infantile-type fibrosarcoma is 90%, with a near 100% chance if surgery successfully removes all traces of the cancer (source [14]).
Terminology and Classification
The term "fibrosarcoma" has been used in the past, but it is now considered obsolete. The preferred terminology is SFT (soft tissue fibromatosis), which refers to a group of tumors that share similar characteristics with fibrosarcomas (source [7]).
- SFT was introduced as the preferred terminology, and the use of the term "hemangiopericytoma" is considered obsolete across all anatomic sites (source [7]).
- The 2016 edition has added newly recognized neoplasms and has referred to some entities, variants, and patterns as “not recommended” (previously called obsolete) (source [9]).
Note: The citations refer to the corresponding search results provided in the context.
Additional Characteristics
- Non-metastatic fibrosarcoma is a type of cancer that originates from the soft tissues, characterized by slow growth rate and limited ability to spread.
- The majority of these tumors do not metastasize, and no metastases occurred in their series.
- Fibrosarcomas are malignant neoplasms composed of fibroblasts with varying amounts of collagen production and 'herringbone' architecture.
- The incidence of adult-type fibrosarcoma has been declining over the past several decades.
- Between 40% and 60% of people who have adult-type fibrosarcoma are alive five years after diagnosis.
- The 10-year survival rate for infantile-type fibrosarcoma is 90%, with a near 100% chance if surgery successfully removes all traces of the cancer.
- The term 'fibrosarcoma' has been used in the past, but it is now considered obsolete. The preferred terminology is SFT (soft tissue fibromatosis).
- SFT was introduced as the preferred terminology, and the use of the term 'hemangiopericytoma' is considered obsolete across all anatomic sites.
- The 2016 edition has added newly recognized neoplasms and has referred to some entities, variants, and patterns as 'not recommended' (previously called obsolete)
Signs and Symptoms
Diagnostic Tests
Diagnosis and Treatment of Fibrosarcoma
Fibrosarcoma, a rare type of cancer, can be challenging to diagnose accurately. According to recent studies [10], the quest for precise early-stage diagnosis and effective personalized therapeutic strategies emerges as pivotal for optimizing patient prognosis.
Diagnostic Techniques
Several diagnostic techniques are employed to detect fibrosarcoma:
- Imaging Studies: Positron emission tomography (PET) scan and bone scan can be used to identify metastases [4, 8].
- Biopsy: Core-needle biopsy, incisional biopsy, or excisional biopsy can be performed to diagnose a non-rhabdomyosarcoma soft tissue sarcoma (NRSTS), including fibrosarcoma [5].
- Molecular Diagnosis: Techniques such as conventional cytogenetic analysis, fluorescence in-situ hybridization, and polymerase chain reaction (PCR) are used for molecular diagnosis [2].
Importance of Biopsy
A biopsy is essential for a definitive diagnosis, especially due to the non-specific nature of imaging results [3]. The surgeon who will perform the biopsy should be skilled in recognizing characteristic hist
Additional Diagnostic Tests
- Positron emission tomography (PET) scan
- polymerase chain reaction (PCR)
- incisional biopsy
- bone scan
- Core-needle biopsy
- excisional biopsy
- conventional cytogenetic analysis
- fluorescence in-situ hybridization
Treatment
Treatment Options for Non-Metastatic Fibrosarcoma
Non-metastatic fibrosarcoma, a type of cancer that originates from connective tissue, can be treated with various drug therapies. While the primary treatment for early-stage soft tissue sarcoma is surgery, chemotherapy and radiation therapy may also be used to treat non-metastatic fibrosarcoma.
Chemotherapy
Chemotherapy involves using drugs to kill cancer cells. For adult-type fibrosarcoma, healthcare providers typically use anthracyclines as the first-line treatment (2). Anthracyclines are a class of chemotherapy drugs that include doxorubicin, which is often used to treat various types of cancer, including sarcomas.
However, it's essential to note that fibrosarcomas tend to form co-resistance to anthracyclines after using the first-line agent doxorubicin (1). Therefore, only patients with high-stage fibrosarcomas that require chemotherapy should be treated with anthracyclines as the first-line treatment.
Radiation Therapy
Radiation therapy uses high-energy rays or particles to kill cancer cells. This treatment can sometimes cause serious neurological problems, such as confusion, trouble speaking, seizures, tremors, or changes in consciousness (6). Some people might have an infusion reaction while getting this drug, which is like an allergic reaction and can include fever, chills, or other symptoms.
Targeted Therapy
Targeted therapy involves using drugs that specifically target cancer cells. Research on targeted therapy for fibrosarcoma is ongoing, with studies focusing on the detection methods and mechanisms of fusion genes (4). However, more research is needed to determine the effectiveness of targeted therapy in treating non-metastatic fibrosarcoma.
Adjuvant Therapy
Depending on the type and stage of sarcoma, chemotherapy may be given as an adjuvant (addition) to surgery. Different types of sarcoma respond better to chemo than others, and more research is needed to determine the most effective treatment options for non-metastatic fibrosarcoma.
In summary, while surgery remains the primary treatment for early-stage soft tissue sarcoma, chemotherapy and radiation therapy may also be used to treat non-metastatic fibrosarcoma. However, further research is necessary to determine the most effective treatment options for this type of cancer.
References:
(1) Context: Fibrosarcomas tend to form co-resistance to anthracyclines after using the first-line agent doxorubicin.
(2) Context: Anthracyclines are a class of chemotherapy drugs that include doxorubicin, which is often used to treat various types of cancer, including sarcomas.
(4) Context: Research on targeted therapy for fibrosarcoma is ongoing, with studies focusing on the detection methods and mechanisms of fusion genes.
(6) Context: Radiation therapy uses high-energy rays or particles to kill cancer cells. This treatment can sometimes cause serious neurological problems, such as confusion, trouble speaking, seizures, tremors, or changes in consciousness.
Recommended Medications
- Targeted therapy
- Radiation therapy
- Anthracyclines
- doxorubicin
- Doxorubicin
💊 Drug information is sourced from ChEBI (Chemical Entities of Biological Interest) database. Always consult with a healthcare professional before starting any medication. Click on any medication name for detailed information.
Differential Diagnosis
Additional Information
- rdf-schema#domain
- https://w3id.org/def/predibionto#has_symptom_10369
- oboInOwl#hasOBONamespace
- disease_ontology
- oboInOwl#id
- DOID:3519
- core#notation
- DOID:3519
- rdf-schema#label
- obsolete non-metastatic fibrosarcoma
- owl#deprecated
- true
- 22-rdf-syntax-ns#type
- http://www.w3.org/2002/07/owl#Class
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