PMID- 2189489 OWN - NLM STAT- MEDLINE DCOM- 19900711 LR - 20190704 IS - 0007-1048 (Print) IS - 0007-1048 (Linking) VI - 74 IP - 4 DP - 1990 Apr TI - Hypercoagulability during L-asparaginase treatment: the effect of antithrombin III supplementation in vivo. PG - 465-70 AB - To evaluate the occurrence of hypercoagulability during treatment with L-asparaginase (L-ase), thrombin-antithrombin complex (TAT) and D-dimer levels in plasma were serially measured in 15 consecutive adult patients with acute lymphoblastic leukaemia or lymphoblastic lymphoma who had recently completed a chemotherapy cycle with cytosine arabinoside and methotrexate. The first eight patients (group A) received i.v. L-ase alone (20,000 U/m2 on alternate days over 10 d); the last seven patients (group B) received, in addition to L-ase, bolus injection of antithrombin concentrate (2000 U) on alternate days for a total of six administrations, beginning with the second L-ase infusion. Increased levels of TAT (P less than 0.05) and D-dimer (P less than 0.01) were observed prior to L-ase, possibly related to inflammation and cytolysis secondary to previous chemotherapy. In patients treated with L-ase alone, further elevation of TAT (P less than 0.05) and persistence of increased D-dimer were observed, associated with marked reduction of the anticoagulant activities of protein C, protein S and antithrombin III. At variance, in patients receiving antithrombin III supplementation there was no increase of TAT and a normalization of D-dimer levels occurred during L-ase treatment. In these patients, mean plasma antithrombin III activity was maintained at levels higher than 70% of normal throughout the treatment. The rate of decline of fibrinogen, factor IX, protein C and protein S was unaffected by antithrombin III supplementation, indicating that hypercoagulability has little if any relevance for the reduction of coagulation factors and inhibitors induced by L-ase treatment. The usefulness of antithrombin III concentrates in preventing thromboembolic complications in patients submitted to L-ase treatment remains to be determined. FAU - Gugliotta, L AU - Gugliotta L AD - Istituto di Ematologia L.eA.Seragnoli, University of Bologna, Italy. FAU - D'Angelo, A AU - D'Angelo A FAU - Mattioli Belmonte, M AU - Mattioli Belmonte M FAU - Vigano-D'Angelo, S AU - Vigano-D'Angelo S FAU - Colombo, G AU - Colombo G FAU - Catani, L AU - Catani L FAU - Gianni, L AU - Gianni L FAU - Lauria, F AU - Lauria F FAU - Tura, S AU - Tura S LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - England TA - Br J Haematol JT - British journal of haematology JID - 0372544 RN - 0 (antithrombin III-protease complex) RN - 9000-94-6 (Antithrombin III) RN - EC 3.4.- (Peptide Hydrolases) RN - EC 3.5.1.1 (Asparaginase) SB - IM MH - Antithrombin III/metabolism/*therapeutic use MH - Asparaginase/*adverse effects/therapeutic use MH - Blood Coagulation Disorders/chemically induced/*prevention & control MH - Humans MH - Lymphoma, Non-Hodgkin/blood/drug therapy MH - Peptide Hydrolases/metabolism MH - Precursor Cell Lymphoblastic Leukemia-Lymphoma/blood/drug therapy EDAT- 1990/04/01 00:00 MHDA- 1990/04/01 00:01 CRDT- 1990/04/01 00:00 PHST- 1990/04/01 00:00 [pubmed] PHST- 1990/04/01 00:01 [medline] PHST- 1990/04/01 00:00 [entrez] AID - 10.1111/j.1365-2141.1990.tb06336.x [doi] PST - ppublish SO - Br J Haematol. 1990 Apr;74(4):465-70. doi: 10.1111/j.1365-2141.1990.tb06336.x.