Twenty‐four patients who developed extramedullary disease during the course of Philadelphia chromosomepositive chronic myelogenous leukemia are described. The most frequent sites of extramedullary disease were lymph nodes (54%), bone (37%), and skin and soft tissue (29%). The appearance of extramedullary disease was associated with a high incidence of other features of accelerated disease (37%) and with cytogenetic clonal evolution (62.5%). The median time from extramedullary disease to blastic crisis was 4 months, and the median survival was 5 months. At the time of analysis, 23 patients have died, 16 after evolving into blastic crisis, and 7 from progressive disease without satisfying the criteria of medullary blastic crisis. This study confirms the importance of extramedullary disease as a sign of poor prognosis in chronic myelogenous leukemia, and the need for alternate therapies when such an event develops. Cancer 59:297–300, 1987. Copyright © 1987 American Cancer Society
CITATION STYLE
Terjanian, T., Kantarjian, H., Keating, M., Talpaz, M., McCredie, K., & Freireich, E. J. (1987). Clinical and prognostic features of patients with philadelphia chromosome‐positive chronic myelogenous leukemia and extramedullary disease. Cancer, 59(2), 297–300. https://doi.org/10.1002/1097-0142(19870115)59:2<297::AID-CNCR2820590221>3.0.CO;2-B
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