Guest guest Posted May 9, 2009 Report Share Posted May 9, 2009 This is a subgroup of leukemias, not something that normally comes up in our posts, some may be interested. Researchers from Iran and France have reported that a regimen of Trisenox® (arsenic trioxide), interferon-alfa, and Retrovir® (zidovudine) is highly effective in patients with adult T-cell lymphoma/leukemia (ATL). The details of this study appeared in an early online publication in Blood on May 1, 2009.[1] http://www.caring4cancer.com/go/cancer/news?NewsItemId=43523 ______________________________ T-Cell Leukemias T cells form part of the body's defense mechanism against disease. T cells originate in bone marrow and then migrate to the thymus gland, where they mature. As they leave the thymus to circulate between the blood and lymph, T cells work to kill specific cells recognized as " foreign, " and to regulate the activities of other cells in fighting disease and infection. Leukemias that affect T cells are very rare; thus, there are no standardized treatments. Various chemotherapy drugs have been tried, both as single agents and in combination, with varying levels of success. The traditional method of diagnosing T-cell leukemias is by looking at the cells under a microscope, as well as by identifying the expression of specific T-cell related molecules on their surface. More recently, highly sensitive techniques demonstrating the clonal nature of the cells are being used. ________________________________ T-Cell Prolymphocytic Leukemia (T-PLL) T-PLL affects prolymphocytes, or T-cells in the intermediate stage of development. Average age of onset is about 63. Symptoms include higher-than-normal white blood cell count, enlarged spleen and swollen lymph nodes. Treatment with pentostatin has had limited success. Alemtuzumab, a monoclonal antibody, is considered the standard treatment for T-PLL, but most patients tend to relapse after treatment. M. D. researchers are studying new drugs and combinations of existing drugs to extend disease-free survival. _________________________________ Adult T-Cell Leukemia/Lymphoma (ATLL) ATLL is caused by the human T-cell leukemia virus Type I, or HTLV-I. An estimated 20-30 million people worldwide are infected with HTLV-I, particularly in Japan, the Caribbean, Central and South America and the southeastern United States. However, only about 2-4% of these " carriers " will develop ATLL. Average age of onset is 58 years, since HTLV-I can remain dormant for up to 30 years before progressing. Because it is a virus, HTLV-I can be transmitted by sexual intercourse, from mother to child through breast milk, or from a transfusion with infected blood. There are four subtypes of ATLL: a.. Acute: The disease progresses quickly. Fifty-seven percent of ATLL patients have the acute form a.. Lymphoma: Involves the lymph nodes, with only minor presence in the blood. Nineteen percent of ATLL patients have this subtype a.. Chronic: This type progresses slowly and is generally more responsive to treatment a.. Smoldering http://www.mdanderson.org/diseases/adultleukemia/display.cfm?id=fa0ad301-68b4-4e\ ca-84918d7ef4d46051 & method=displayfull FYI, Lottie Quote Link to comment Share on other sites More sharing options...
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