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Blastic transformation in chronic myelogenous leukemia: Experience with 50 patients

✍ Scribed by Marks, Stanley M. ;McCaffrey, Ronald ;Rosenthal, David S. ;Moloney, William C.


Publisher
John Wiley and Sons
Year
1978
Tongue
English
Weight
518 KB
Volume
4
Category
Article
ISSN
0098-1532

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✦ Synopsis


Abstract

Fifty consecutive patients with blastic chronic myelogenous leukemia were evaluated clinically, morphologically, biochemically, and therapeutically. Forty‐five patients had a preceding stable phase (38 Ph +, 7 Ph ‐); five patients presented with de novo Ph+ blast crisis. The most frequent clinical signs of impending blast crisis were weakness, fatigue, increasing splenomegaly, anemia, thrombocytopenia, marrow fibrosis, and a rising neutrophil alkaline phosphatase. Fever (unrelated to infection), skin infiltration, lymphadenopathy, hepatomegaly, thrombocytosis, and basophilia were much less common. The development of aneuploidy occurred in less than one‐half of the total group. Myeloblastic morphology at blastic transformation was most frequent with occasional lymphoblastic, promyelocytic, and undifferentiated cases seen. Terminal deoxynucleotidyl transferase was present in one‐third of the patients, but had no clear‐cut relationship to the morphology. Response to treatment was generally disappointing (two complete and 15 partial remissions in 45 treated patients).


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Blastic crisis in chronic granulocytic l
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In a n attempt to prolong survival, a group of 39 adult patients with chronic granulocytic leukemia in acute transformation was treated with intensive chemotherapy regimens which included the use of single agents o r drug combinations. An over-all remission rate of 28% was obtained, with only 10% of