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.
引用
收藏
页码:790 / 798
页数:9
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