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Clinical lymphoma & myeloma · 2005

T-cell prolymphocytic leukemia: a single-institution experience.

СтатьяНазвание и аннотация: Перевод в очереди
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Ravandi Farhad, O'Brien Susan, Jones Dan, Lerner Susan, Faderl Stefan, Ferrajoli Alessandra, Wierda William, Garcia-Manero Guillermo, Thomas Deborah, Koller Charles, Verstovsek Srdan, Giles Francis, Cortes Jorge, Herling Marco, Kantarjian Hagop, Keating Michael

Аннотация

BACKGROUND: T-cell prolymphocytic leukemia is an uncommon, aggressive, mature T-cell leukemia characterized by proliferation of T-cell lymphocytes. The recent availability of modern immunophenotypic and molecular tools has allowed a better distinction of this disorder from its B-cell counterpart and other mature T-cell leukemias.

PATIENTS AND METHODS: The clinical, pathologic, and cytogenetic features of 57 patients with T-PLL who were evaluated at the Department of Leukemia, M. D. Anderson Cancer Center (MDACC) from 1986 to 2004 were examined.

RESULTS: The most common cytogenetic abnormality was inv(14)(q11;q32), which was present in 7 patients. In all 7 patients, this abnormality was associated with other chromosomal aberrations. Patients treated with alemtuzumab at MDACC had a significantly better response rate (P = 0.02) and survival rate (P = 0.002). There were no significant differences in survival based on Tcl-1 expression or different patterns of CD4 and CD8 expression.

CONCLUSION: Treatment with alemtuzumab results in higher response rates and a better survival rate in patients with T-cell prolymphocytic leukemia.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты