Leukemia - Chronic T-Cell Lymphocytic


Lesson on Chronic lymphocytic leukemia (CLL) and the related non-Hodgkin Lymphoma small lymphocytic Lymphoma (SLL). CLL is the most common adult leukaemia in the western world, and affects older adults most often. CLL is a blood cancer involving mature lymphocytes. Often times CLL is detected on a routine blood test and can be asymptomatic; however, characteristic physical findings includes lymphadenopathy among others. Laboratory blood findings and physical exam findings can also help us distinguish between CLL and SLL. Staging of this condition can also help us determine when to treat it, and the genetic profile of the cancer helps us determine what is the appropriate treatment for this cancer.
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Adult T-cell leukemia/lymphoma is associated with human T-cell leukemia virus-1 (HTLV-1)...It's prevalent in Japan, South America, West Africa, and the Caribbean.
Human T- cell leukemia virus -1 (HTLV-1) is a retrovirus that can be transmitted through IV drug abuse.
Hematological malignancies can be divided into leukemias, lymphomas, and multiple myeloma.
Lymphomas can be divided into Hodgkin's lymphoma and non-Hodgkin's lymphoma.
Non-Hodgkin's lymphoma can be subdivided into aggressive lymphoma and indolent lymphoma.
Aggressive non-Hodgkin's lymphomas include:
*Diffuse large B-cell lymphoma (DLBCL)
*Burkitt's lymphoma.
*Mantle cell lymphoma.
*Precursor T-cell lymphoblastic lymphoma.
*B-lymphoblastic lymphoma.
Indolent non-Hodgkin's lymphomas include:
*Follicular lymphoma
*Marginal zone B-cell lymphoma (MALToma)
*Hairy cell leukemia/ lymphoma.
*Waldenstrom macroglobulinemia.
*Mycosis fungoides/ Sezary syndrome.
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Researchers at Penn's Abramson Cancer Center have molecularly engineered T-cells from patients with chronic lymphocytic leukemia and achieved an exceptional, unprecedented antitumor response.
In the pilot study of three patients, two achieved complete remission and the third experienced remarkable antitumor response, which was impossible with previously available treatments. The modified T-cells mimic bone marrow transplant (BMT), but without the associated risks.
The result of integration between the research lab and clinic, this study is the first time that researchers have shown that T-cells can function as serial tumor kills. In the pilot study, the modified T-cells eradicated at least 1,000 tumor cells in each patient.
Contrary to other treatments, such as chemotherapy, the modified T-cells are only released into the body once. They persist, divide and continue to kill tumor cells on their own.
View the full news release from Penn Medicine: http://www.uphs.upenn.edu/news..../News_Releases/2011/