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Blood, Vol. 96 No. 2 (July 15), 2000: pp. 768-770

BRIEF REPORT


Clinical relevance of intracellular vascular endothelial growth factor levels in B-cell chronic lymphocytic leukemia

Alvaro Aguayo, Susan O'Brien, Michael Keating, Taghi Manshouri, Cristi Gidel, Bart Barlogie, Miloslav Beran, Charles Koller, Hagop Kantarjian, and Maher Albitar

From the Departments of Leukemia and Hematopathology, University of Texas MD Anderson Cancer Center, Houston, TX, and the Myeloma and Transplantation Research Center, University of Arkansas for Medical Sciences, Little Rock, AR.

Strong evidence exists for an association between high vascular endothelial growth factor (VEGF) levels and poor prognoses in patients with solid tumors and acute leukemia. Using Western blot analysis and solid-phase radioimmunoassay, we measured cellular VEGF levels in B-cell chronic lymphocytic leukemia (CLL) samples from 225 patients and correlated these levels with disease characteristics and prognoses. The median VEGF level in CLL samples was 7.26 times the median level detected in normal peripheral blood mononuclear cells. Patients with lower levels of VEGF protein showed a trend toward shorter survival (P = .07). However, in a subgroup of CLL patients with good prognoses or early-stage disease (Rai stages 0-II, Binet stages A,B; beta 2-M <=  2.8 mg/dL), lower levels of VEGF were associated with shorter survival times. For the entire group of patients, no correlation was found between VEGF levels and beta 2-M levels or Rai and Binet stage. Most samples from patients with CLL expressed the 43-kd VEGF isoform in addition to the commonly expressed 45-kd isoform. It remains to be seen whether the expression of the 43-kd isoform is responsible for this reversed correlation with outcome.


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