TY - JOUR
T1 - Hypoalbuminemia for the prediction of venous thromboembolism and treatment of direct oral anticoagulants in metastatic gastric cancer patients
AU - Takayoshi, Kotoe
AU - Kusaba, Hitoshi
AU - Aikawa, Tomomi
AU - Koreishi, Sakuya
AU - Sagara, Kosuke
AU - Nakano, Michitaka
AU - Komoda, Masato
AU - Kono, Mihoko
AU - Fukata, Mitsuhiro
AU - Arita, Takeshi
AU - Esaki, Taito
AU - Akashi, Koichi
AU - Baba, Eishi
N1 - Funding Information:
Conflict of interest M. Kono has received grants from Pfizer Japan Inc. M. Fukata has received grants from Shino-Test Corporation; personal fees from Pfizer, Daiichi Sankyo Company, Bayer Yakuhin, and Boehringer Ingelheim. T. Esaki has received grants and personal fees from Eli Lilly, Taiho, Daiichi-Sankyo, Merck Serono, and Ono; grants from Novartis, DS pharma, MSD and Boehringer; personal fees from Chugai, Bristol, Eisai and Takeda. K. Akashi has received grants and personal fees from Mitsubishi Tanabe Pharma Corporation, Daiichi-Sankyo, MSD, Eisai, Astellas Pharma, Sanofi, Chugai Pharmaceutical, Asahi Kasei Pharma, Kyowa Hakko Kirin, Sumitomo Dainippon Pharma, Bristol-Myers Squibb, Takeda Pharmaceutical, Novartis Pharma, Alexion Pharmaceuticals, Teijin Pharma, Nippon Shinyaku, Yakult Honsha, Mundipharma and Bayer Yakuhin; grants from Ono Pharmaceutical, Merck Serono, Toyama Chemical, Taiho Pharmaceutical, Otsuka Pharmaceutical, Yakult Honsha Co, AbbVie, Shionogi, Eli Lilly Japan, Taisho Toyama Pharmaceutical, Mochida Pharmaceutical, The Chemo-Sero-Therapeutic Research Institute., Merck Serono, Nippon Kayaku, Japan Blood Products Organization, and Shin Nippon Biomedical Laboratories; personal fees from Celgene, Janssen Pharmaceutical, Pfizer, Medical Review, Amgen Astellas Biopharma and Shire Japan. E. Baba has received grants, personal fees and nonfinancial support from Eli Lilly Japan; grants and personal fees from Daiichi-Sankyo, Bristol-Myers Squibb, Taiho Pharmaceutical. Eisai, Yakult Honsha, and Ono Pharmaceutical; grants from Bayer Yakuhin, MSD, Linical; personal fees from Takeda Pharmaceutical, Sumitomo Dainippon Pharma, Kyowa Hakko Kirin, Sanofi, Merck Serono, Tsumura, Chugai Pharmaceutical, and Astellas Pharma. All of the remaining authors declare that they have no conflicts of interest.
Publisher Copyright:
© 2019, The International Gastric Cancer Association and The Japanese Gastric Cancer Association.
PY - 2019/9/5
Y1 - 2019/9/5
N2 - Background: Venous thromboembolism (VTE) is highly associated with advanced gastric cancer (AGC) and is sometimes lethal. Predictors of VTE have not been identified, and the efficacy and safety of direct oral anticoagulants (DOACs) for AGC-associated VTE remain to be clarified. Methods: A total of 188 AGC patients who started chemotherapy during the period from January 2014 to December 2017 in our institutions were retrospectively examined for the incidence of VTE, risk factors for VTE, and the efficacy and safety of DOAC-based anticoagulant therapy for VTE. Results: Thirty-four patients (18%) were diagnosed with VTE at the start or during the course of chemotherapy (VTE group). More VTE group patients had a history of abdominal surgery and had moderate–severe ascites (32% versus 17%, 32% versus 14%, respectively) than non-VTE group patients (NVTE group). The mean serum albumin concentrations in the VTE group were significantly lower than NVTE group (3.38 mg/dL vs 3.65 mg/dL, respectively). Multivariate analysis showed that hypoalbuminemia was significantly correlated with VTE (P = 0.012). In the VTE group, 29 patients (85%) received anticoagulant therapy, including 24 patients treated with DOACs. No lethal VTE was observed in any patients. Thirteen patients (45%) terminated DOACs because of anemia or bleeding events, of whom eleven developed major bleeding. Median overall survivals of the VTE and NVTE groups were 9.63 months and 11.5 months, respectively (P = 0.262). Conclusion: Hypoalbuminemia appears to be a risk factor for AGC-associated VTE. DOACs are effective to AGC-associated VTE, but careful observation of bleeding events is required.
AB - Background: Venous thromboembolism (VTE) is highly associated with advanced gastric cancer (AGC) and is sometimes lethal. Predictors of VTE have not been identified, and the efficacy and safety of direct oral anticoagulants (DOACs) for AGC-associated VTE remain to be clarified. Methods: A total of 188 AGC patients who started chemotherapy during the period from January 2014 to December 2017 in our institutions were retrospectively examined for the incidence of VTE, risk factors for VTE, and the efficacy and safety of DOAC-based anticoagulant therapy for VTE. Results: Thirty-four patients (18%) were diagnosed with VTE at the start or during the course of chemotherapy (VTE group). More VTE group patients had a history of abdominal surgery and had moderate–severe ascites (32% versus 17%, 32% versus 14%, respectively) than non-VTE group patients (NVTE group). The mean serum albumin concentrations in the VTE group were significantly lower than NVTE group (3.38 mg/dL vs 3.65 mg/dL, respectively). Multivariate analysis showed that hypoalbuminemia was significantly correlated with VTE (P = 0.012). In the VTE group, 29 patients (85%) received anticoagulant therapy, including 24 patients treated with DOACs. No lethal VTE was observed in any patients. Thirteen patients (45%) terminated DOACs because of anemia or bleeding events, of whom eleven developed major bleeding. Median overall survivals of the VTE and NVTE groups were 9.63 months and 11.5 months, respectively (P = 0.262). Conclusion: Hypoalbuminemia appears to be a risk factor for AGC-associated VTE. DOACs are effective to AGC-associated VTE, but careful observation of bleeding events is required.
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U2 - 10.1007/s10120-019-00930-2
DO - 10.1007/s10120-019-00930-2
M3 - Article
C2 - 30788749
AN - SCOPUS:85061810046
SN - 1436-3291
VL - 22
SP - 988
EP - 998
JO - Gastric Cancer
JF - Gastric Cancer
IS - 5
ER -