Peripheral T-cell Lymphoma Samples
Peripheral T-cell Lymphoma (PTCL) Overview
Stages of Peripheral T-cell Lymphoma (PTCL)
Scientists have developed a staging system that helps healthcare professionals know the extent of cancer spread. The Lugano classification consists of four stages, indicated as Roman numerals I–IV. When the lymphoma has affected an organ outside the lymphatic system (extra lymphatic organ), an E is added to the stage, for example, IIE.
Stage I
- I: The cancer is limited to one lymph node or lymphoid organ.
- IE: The cancer is only in one area of a single organ outside the lymph system.
Stage II
- II: The cancer is in two or more lymph nodes in the region of the diaphragm (above or below).
- IIE: The cancer is in one organ and its regional lymph nodes. It may or may not affect other groups of lymph nodes on the same side of the diaphragm.
Stage III
- The cancer is in the lymph node areas on both sides of the diaphragm (above and below).
- The cancer is in the lymph nodes found above the diaphragm and in the spleen.
Stage IV
- The cancer has spread throughout the body outside the lymph system, commonly in the liver, lungs, or bone marrow.
Stages I and II and stage II non-bulky are under limited or localized diseases, while stages III and IV are considered advanced.
Signs and Symptoms of Peripheral T-cell Lymphoma (PTCL)
- Armpit
- Either side of the neck
- Elbows
- Near the ears
- On the back of the knees
- The groin
These are not the same as reactive lymph nodes, which increase in size due to infection. Aside from lymph nodes, PTCL can affect organs such as the skin, liver, spleen, and stomach, which may cause the following:
- An enlarged belly that can be painful
- Bruising and bleeding
- Chest pain or pressure
- Cough
- Extreme tiredness and fatigue
- Feeling of fullness
- Frequent infections
- Nausea
- Shortness of breath
- Vomiting
Some patients may experience the three “B symptoms,” which are drenching night sweats, fever that come and go, sometimes for weeks, and unexplained weight loss.
Causes of Peripheral T-cell Lymphoma (PTCL)
The causes of why peripheral T-cell lymphoma (PTCL) develop is unknown. However, research from 2020 states that changes in the DNA’s structure causing abnormal gene expression (epigenetic alterations) have an essential role in the development of certain types of PTCL.
Certain conditions may cause alterations in the DNA of lymphocytes or increase the chances for mutations to occur. These conditions include long-term, viral, and bacterial infections.
- Electrical fitters
- Individuals who have smoked for over 40 years
- Textile workers
Diagnosis of Peripheral T-cell Lymphoma (PTCL)
To make a diagnosis of peripheral T-cell lymphoma (PTCL, a doctor conducts a medical history and a physical examination, paying close attention to the patient’s clinical information. If a doctor suspects the patient has lymphoma, they will request a lymph node biopsy, where a healthcare professional removes part or the entire lymph node for lab analysis.
Sometimes, a doctor may also ask for other samples, such as a bone marrow biopsy and a cerebrospinal fluid (CSF) analysis, also known as a spinal tap.
Specialists may request additional tests to identify the type of PTCL a person has. These include:
- Flow cytometry and immunophenotyping. This test looks for specific proteins or markers in cells that can identify the type of lymphocyte and how mature the lymphocyte is.
- Chromosome tests. Cytogenetic studies, fluorescent in situ hybridization, and polymerase chain reaction tests detect genetic and chromosomal changes in cells.
Treatment of Peripheral T-cell Lymphoma (PTCL)
Usually newly diagnosed PTCL patients are treated with anthracycline-based chemotherapy regimens. The general practice is to treat the disease whether it is limited or advanced. For stage II bulky lymphomas, doctors need to consider other prognostic factors to determine if it is limited or advanced.
Drug Combinations
While PTCL has no standard of care, most subtypes receive an initial treatment of a combination chemotherapy regimen. The regimens are most commonly CHOP (cyclophosphamide, hydroxydoxorubicin, vincristine, prednisone) or other multidrug combinations such as CHOEP (CHOP plus etoposide) and EPOCH (etoposide, vincristine, doxorubicin, cyclophosphamide, and prednisone).
Stem Cell Transplants
Other Therapies
Healthcare providers may give antiviral drugs to patients with PTCL caused by viruses in addition to a chemotherapy regimen. Those with localized PTCL, such as extranodal NK/T-cell lymphoma and angioimmunoblastic T-cell lymphoma, may benefit from radiation therapy. Some may also benefit from chemotherapy with radiation (chemoradiation).
Prognosis of Peripheral T-cell Lymphoma (PTCL)
The outcome of PTCL is generally poor except for anaplastic large cell lymphoma and anaplastic lymphoma kinase. Treatment outcomes with conventional therapy have also been poor.
However, advances in genetic and molecular testing techniques and a greater understanding of PTCL disease have led to the development of new drugs that are currently under study and trials.
Doctors use the International Prognostic Index (IPI) to help them determine the outlook and overall survival in individuals with aggressive lymphomas, such as PTCL. It can also help them decide on the appropriate care and predict the risk of relapse.
The IPI includes the following five factors:
- Patient’s age
- Stage of lymphoma
- Presence of lymphoma in organs outside the lymph system (extralymphatic organ)
- Levels of lactate dehydrogenase in the blood, which increase according to the amount of lymphoma in the body
- Performance status, or the patient’s ability to function in everyday activities
- Peripheral whole-blood
- Amniotic fluid
- Bronchoalveolar lavage fluid (BAL)
- Sputum
- Pleural effusion
- Cerebrospinal fluid (CSF)
- Serum (sera)
- Plasma
- Peripheral blood mononuclear cells (PBMC)
- Saliva
- Buffy coat
- Urine
- Stool samples
- Aqueous humor
- Vitreous humor
- Kidney stones (renal calculi)
- Other bodily fluids from most diseases including cancer.
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