Volume 46, Issue 3 pp. 184-188
Original Article
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Rapid improvement of coagulopathy by all-trans retinoic acid in acute promyelocytic leukemia

Dr. Yohko Kawai

Corresponding Author

Dr. Yohko Kawai

Department of Laboratory Medicine, Keio University School of Medicine, Tokyo, Japan

Keio University School of Medicine, Department of Laboratory Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, Japan 160Search for more papers by this author
Kiyoaki Watanabe

Kiyoaki Watanabe

Department of Laboratory Medicine, Keio University School of Medicine, Tokyo, Japan

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Masahiro Kizaki

Masahiro Kizaki

Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

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Mitsuru Murata

Mitsuru Murata

Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

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Tetsuji Kamata

Tetsuji Kamata

Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

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Hideo Uchida

Hideo Uchida

Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

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Takanori Moriki

Takanori Moriki

Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

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Kenji Yokoyama

Kenji Yokoyama

Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

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Michihide Tokuhira

Michihide Tokuhira

Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

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Hideaki Nakajima

Hideaki Nakajima

Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

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Makoto Handa

Makoto Handa

Blood Center, Keio University School of Medicine, Tokyo, Japan

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Yasuo Ikeda

Yasuo Ikeda

Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

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First published: July 1994
Citations: 27

Abstract

Treatment of acute promyelocytic leukemia (APL) patients with all-trans retinoic acid (ATRA) was associated with rapid improvement in hemostatic markers. We made serial analyses of various hemostatic parameters in seven newly diagnosed APL patients. In all patients at diagnosis, plasma fibrinogen/fibrin degradation product (fragment-E), cross-linked fibrin degradation product (D-dimer fragment), thrombin-antithrombin III complex and plasmin-α2-plasmin inhibitor complex were elevated, indicating the presence of disseminated intravascular coagulation (DIC). Antithrombin III (A TIII) levels were normal in all patients except for the patient with congenital ATIII deficiency. In four patients subsequently treated with ATRA without anticoagulant therapy, these hemostatic markers returned to near-normal levels by day 7 of treatment, indicating that DIC was essentially resolved. By contrast, in three patients who received conventional chemotherapy with a continuous low-dose heparin, improvement of coagulopathy was slower than in patients treated with ATRA. These results suggest that ATRA therapy exerts the rapid improvement in abnormal hemostatic markers in APL patients without any anticoagulant therapies, by inducing differentiation of leukemic cells and, in turns no massive release of procoagulant or fibrinolytic substances from these cells. © 1994 Wiley-Liss, Inc.

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