Assessment of Coagulation Disorders in Patients with Acute Leukemia Before and After Cytostatic Treatment

• Published in: Leukemia & lymphoma Vol. 36; no. 1-2; pp. 77 - 84
• Main Authors: Chojnowski, Krzysztof, Wawfuyniak, Ewa, Treilinski, Jacek, Niewiarowska, Jolanta, Cierniewski, Czeslaw
• Format: Journal Article
• Language: English
• Published: United States Informa UK Ltd 1999; Taylor & Francis
• Subjects: acute leukemia; Adolescent; Adult; Antithrombin III - analysis; Blood Coagulation; Blood Coagulation Disorders - etiology; coagulation activation markers; coagulation disorders; DIC; Disseminated Intravascular Coagulation - etiology; Female; Fibrin Fibrinogen Degradation Products - analysis; hemorrhage; Humans; Leukemia, Myeloid, Acute - blood; Leukemia, Myeloid, Acute - complications; Leukemia, Myeloid, Acute - drug therapy; Male; Middle Aged; Peptide Hydrolases - analysis; Precursor Cell Lymphoblastic Leukemia-Lymphoma - blood; Precursor Cell Lymphoblastic Leukemia-Lymphoma - complications; Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy
• ISSN: 1042-8194; 1029-2403
• DOI: 10.3109/10428199909145951

Coagulation disorders are often the reason for fatal bleeding in acute promyelocytic leukemia. Their occurrence as well as pathogenesis and prognostic significance in other subtypes of acute myelogenous leukemia and acute lymphoblastic leukemia is less known. Tests were carried out in 70 patients including 49 with AML and 21 with ALL. In all patients throm-bin-antithrombin complexes (TAT), D-dimer (DD) and plasmin-antiplasmin complexes (PAP), antithrombin 111 activity, fibrinogedfibrin degradation products, AFlT and PT were determined. The tests were performed on diagnosis and after cytostatic treatment. The level of TAT, DD and PAP was elevated in 83% of the patients on diagnosis and in 90% after treatment. The highest values were observed in AML M3 patients. Among leuke-mic patients with normal levels of TAT, DD and PAP at diagnosis, cytostatic treatment had a negligible effect on the level of these markers. During remission the levels of these markers returned to the normal values while in patients without remission they were either elevated or returned to normal values. No correlation between the levels of activation markers and remission rate was reported. DIC was diagnosed in 13 patients including three after chemotherapy. The DIC was acute or subacute in AML and chronic in ALL patients. In the majority of acute leukemia patients there were already changes on diagnosis indicating coagulation activation. Except for AML M3, these usually had a subclinical course. The TAT, DD and PAP tests are not reliable markers of remission in acute leukemias.