Retrospective analysis on the clinical outcomes of recombinant human soluble thrombomodulin for disseminated intravascular coagulation syndrome associated with solid tumors

被引:15
作者
Ouchi, Kota [1 ,2 ]
Takahashi, Shin [1 ,2 ]
Chikamatsu, Sonoko [1 ,2 ]
Ito, Shukuei [1 ,2 ]
Takahashi, Yoshikazu [3 ]
Kawai, Sadayuki [3 ]
Okita, Akira [1 ,2 ]
Kasahara, Yuki [1 ,2 ]
Okada, Yoshinari [1 ,2 ]
Imai, Hiroo [1 ,2 ]
Komine, Keigo [1 ,2 ]
Saijo, Ken [1 ,2 ]
Takahashi, Masahiro [1 ,2 ]
Shirota, Hidekazu [1 ,2 ]
Takahashi, Masanobu [1 ,2 ]
Gamoh, Makio [3 ]
Ishioka, Chikashi [1 ,2 ]
机构
[1] Tohoku Univ Hosp, Dept Med Oncol, Sendai, Miyagi, Japan
[2] Tohoku Univ, Inst Dev Aging & Canc, Dept Clin Oncol, Aoba Ku, 4-1 Seiryo Machi, Sendai, Miyagi 9808575, Japan
[3] Osaki Citizen Hosp, Dept Med Oncol, Osaki, Japan
关键词
Disseminated intravascular coagulation; Recombinant human soluble thrombomodulin; Solid tumors; CANCER-PATIENTS; ACTIVATION; TRIAL; TREAT;
D O I
10.1007/s10147-018-1261-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recombinant human soluble thrombomodulin (rTM) has been established and introduced in the clinic as a standard treatment for disseminated intravascular coagulation (DIC). However, the efficacy and safety of rTM for DIC associated with solid tumors (DIC-STs) have not been fully established. Here, we performed a retrospective analysis of the clinical outcomes of rTM for DIC-STs and considered a treatment strategy with rTM for DIC-STs. Patients with DIC-STs between November 2009 and March 2016 in 2 cancer core hospitals were retrospectively analyzed. Data, including patient background, treatment course, and clinical outcomes of rTM for DIC-STs, were extracted. The clinical outcomes were evaluated by comparing the DIC score, resolution rate, and overall survival (OS) duration. The study included 123 patients with DIC-STs. The median OS in all patients was 41 days. The DIC resolution rate was 35.2%. DIC scores and DIC-related blood test data (fibrin degradation product and prothrombin time-international normalized ratio) significantly improved at the end of rTM administration (P < 0.001). The OS duration was longer in patients who were treated with chemotherapy after DIC onset than in those who were not treated with chemotherapy (median, 178 days vs. 17 days, P < 0.001). In both univariate and multivariate analyses, chemotherapy after DIC onset showed the strongest association with OS. rTM can at least temporarily improve or maintain the state of DIC-STs. It is suggested that prolongation of survival can be expected when control of DIC and treatment of the underlying disease are compatible.
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收藏
页码:790 / 798
页数:9
相关论文
共 16 条
  • [1] AMBRUS JL, 1975, J MED, V6, P61
  • [2] Asano Yuka, 2014, Gan To Kagaku Ryoho, V41, P2503
  • [3] EXTRINSIC-PATHWAY ACTIVATION IN CANCER WITH HIGH FACTOR VIIA AND TISSUE FACTOR
    KAKKAR, AK
    DERUVO, N
    CHINSWANGWATANAKUL, V
    TEBBUTT, S
    WILLIAMSON, RCN
    [J]. LANCET, 1995, 346 (8981): : 1004 - 1005
  • [4] Prospective evaluation of hemostatic abnormalities in overt DIC due to various underlying diseases
    Kawasugi, Kazuo
    Wada, Hideo
    Hatada, Tsuyoshi
    Okamoto, Kohji
    Uchiyama, Toshimasa
    Kushimoto, Shigeki
    Seki, Yoshinobu
    Okamura, Takashi
    Nobori, Tsutomu
    [J]. THROMBOSIS RESEARCH, 2011, 128 (02) : 186 - 190
  • [5] Kazmierczak M, 2005, BLOOD COAGUL FIBRIN, V16, P543
  • [6] Kobayashi N, 1983, Bibl Haematol, P265
  • [7] Disseminated intravascular coagulation: Treat the cause, not the lab values
    Labelle, CA
    Kitchens, CS
    [J]. CLEVELAND CLINIC JOURNAL OF MEDICINE, 2005, 72 (05) : 377 - +
  • [8] Current concepts - Disseminated intravascular coagulation
    Levi, M
    ten Cate, H
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (08) : 586 - 592
  • [9] Disseminated intravascular coagulation in cancer patients
    Levi, Marcel
    [J]. BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY, 2009, 22 (01) : 129 - 136
  • [10] Lin PH, 2010, ANTICANCER RES, V30, P3087