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Thrombomodulin alfa treatment in patients with acute promyelocytic leukemia and disseminated intravascular coagulation: A retrospective analysis of an open-label,multicenter, post-marketing surveillance study cohort
Authors:Tadashi Matsushita  Jyunichi Watanabe  Goichi Honda  Jun Mimuro  Hoyu Takahashi  Hajime Tsuji  Yutaka Eguchi  Isao Kitajima  Yoichi Sakata
Affiliation:1. Department of Transfusion Medicine, Nagoya University Hospital, Aichi, Japan;2. ART Project, Asahi Kasei Pharma Corporation, Tokyo, Japan;3. Division of Cell and Molecular Medicine, Center for Molecular Medicine, Jichi Medical University, School of Medicine, Tochigi, Japan;4. Department of Internal Medicine, Niigata Prefectural Kamo Hospital, Niigata, Japan;5. Department of Blood Transfusion, Kyoto Prefectural University of Medicine, Kyoto, Japan;6. Critical and Intensive Care Medicine, Shiga University of Medical Science, Shiga, Japan;g Department of Clinical Laboratory and Molecular Pathology, Graduate School of Medical and Pharmaceutical Science, University of Toyama, Toyama, Japan;h The Japanese Society on Thrombosis and Hemostasis Post-Marketing Surveillance Committee for Recomodulin® Injection, Japan
Abstract:

Introduction

Patients with acute promyelocytic leukemia (APL) can develop disseminated intravascular coagulation (DIC) that results in life-threatening hemorrhagic complications. Studies regarding the safety and efficacy of thrombomodulin alfa (TM-α; recombinant human soluble thrombomodulin) in patients with APL and DIC are limited.

Materials and methods

A retrospective evaluation was performed on a cohort of 172 patients with APL from an open-label, multicenter, post-marketing surveillance study of TM-α.

Results

Of the 172 patients, 31 were relapse/refractory APL patients, and 141 were newly diagnosed APL patients. Within the first 30 days, 24 patients (14.0%) died, and six of those deaths (3.5%) were due to hemorrhage. In total, 12 patients (7.0%) had severe hemorrhagic complications. Both the early death rate due to hemorrhage as well as the severe hemorrhage rate did not exceed those in some recent population-based studies of patients with APL. Forty-nine patients received TM-α prior to the initiation of antileukemic treatment, and one patient experienced hemorrhagic early death (ED), suggesting that early TM-α treatment appeared to result in a reduction in the hemorrhagic ED rate. Moreover, TM-α improved coagulopathy regardless of concomitant all-trans retinoic acid treatment.

Conclusions

This study confirmed the safety and efficacy of TM-α in daily clinical practice for patients with APL and DIC. TM-α appeared to reduce hemorrhagic early deaths due to DIC in patients with APL who were receiving antileukemic treatment.
Keywords:APL, acute promyelocytic leukemia   AML, acute myelogenous leukemia   PML, promyelocytic leukemia   RARα, retinoic acid receptor-α   DIC, disseminated intravascular coagulation   ATRA, all-trans retinoic acid   ED, early death   TM, thrombomodulin   JALSG, Japan Adult Leukemia Study Group   CNS, central nervous system   FDP, fibrin and fibrinogen degradation products   PT, prothrombin time   APTT, activated partial thromboplastin time   TAT, thrombin-antithrombin complex   PIC, plasmin-plasmin inhibitor complex   AT, antithrombin   PC, protein C   JMHW, Japanese Ministry of Health and Welfare   WBC, white blood cell   LDH, lactate dehydrogenase   AST, aspartate aminotransferase   ALT, alanine aminotransferase   PETHEMA, Programa para el Estudio y Tratamiento de las Hemopatias Malignas   ISTH, International Society of Thrombosis and Hemostasis   TAFI, thrombin-activatable fibrinolysis inhibitor   t-PA, tissue-type plasminogen activator
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