TY - JOUR
T1 - Retrospective analysis on the clinical outcomes of recombinant human soluble thrombomodulin for disseminated intravascular coagulation syndrome associated with solid tumors
AU - Ouchi, Kota
AU - Takahashi, Shin
AU - Chikamatsu, Sonoko
AU - Ito, Shukuei
AU - Takahashi, Yoshikazu
AU - Kawai, Sadayuki
AU - Okita, Akira
AU - Kasahara, Yuki
AU - Okada, Yoshinari
AU - Imai, Hiroo
AU - Komine, Keigo
AU - Saijo, Ken
AU - Takahashi, Masahiro
AU - Shirota, Hidekazu
AU - Takahashi, Masanobu
AU - Gamoh, Makio
AU - Ishioka, Chikashi
N1 - Funding Information:
Conflict of interest Chikashi Ishioka has received research funding from the Tokyo Cooperative Oncology Group. Chikashi Ishioka has also received contributions from Chugai Pharmaceutical, Ono pharmaceutical, MSD, Phizer, AstraZeneca, Bristol-Myers squibb, Janssen Pharmaceutical, Taiho Pharmaceutical, Daiichi Sankyo Company, Limited, and Takeda Pharmaceutical. Shin Takahashi has received research funding from Merck Serono Company. Masanobu Takahashi has received research funding from Ono Pharmaceutical Company. Masanobu Takahashi is a member of a committee of Tohoku Clinical Oncology Research and Education Society, a specified non-profit corporation. Chikashi Ishioka is a representative of Tohoku Clinical Oncology Research and Education Society, a specified non-profit corporation.
Publisher Copyright:
© 2018, Japan Society of Clinical Oncology.
PY - 2018/8/1
Y1 - 2018/8/1
N2 - Background: 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. Methods: 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. Results: 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. Conclusions: 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.
AB - Background: 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. Methods: 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. Results: 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. Conclusions: 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.
KW - Disseminated intravascular coagulation
KW - Recombinant human soluble thrombomodulin
KW - Solid tumors
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U2 - 10.1007/s10147-018-1261-z
DO - 10.1007/s10147-018-1261-z
M3 - Article
C2 - 29511940
AN - SCOPUS:85050923008
SN - 1341-9625
VL - 23
SP - 790
EP - 798
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 4
ER -