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Safety and feasibility of lower antithrombin replacement targets in adult patients with hematological malignancies receiving asparaginase therapy<sup/>.

Jason N BarretoKristen B McCulloughCandy S PeskeyRoss A DierkhisingKristin C MaraMichelle A ElliottDennis A GastineauAref A Al-KaliNaseema GangatLouis LetendreWilliam Joseph HoganMark R LitzowMirinal S Patnaik
Published in: Leukemia & lymphoma (2017)
The optimal antithrombin(AT) activity parameters for replacement as thromboprophylaxis following asparaginase remains unclear. This single-center, retrospective study evaluated two sets of AT replacement thresholds and targets in adults receiving asparaginase-containing chemotherapy. AT supplementation adhered to institutional standards, which lowered the AT activity target from 100% to 80% in 6/2014. Ninety-two patients were evaluated. Cumulative thrombosis incidence was 16% at 6 months (95%CI:6.8-24.0, maximum follow-up 315 days) with similar incidence between the 80% and 100% target groups, 14% (2 of the 14) and 13% (10 of the 78), respectively, with a small non-Line-Related DVT incidence (3%). Most thrombotic events occurred during induction chemotherapy and demonstrated no associations with replacement target, cumulative days or cumulative area under AT activity target, number of asparaginase doses, or cumulative asparaginase dose. Median estimated AT replacement expenditure was $34,963USD (IQR $16,260USD to $79,319USD) per patient. Cost-effectiveness and optimization of AT replacement for thromboprophylaxis following asparaginase requires prospective evaluation.
Keyphrases
  • risk factors
  • end stage renal disease
  • chronic kidney disease
  • newly diagnosed
  • squamous cell carcinoma
  • locally advanced
  • prognostic factors
  • pulmonary embolism
  • peritoneal dialysis
  • drug induced
  • smoking cessation