TY - JOUR
T1 - Symptomatic Venous Thromboembolism in Patients with Malignant Bone and Soft Tissue Tumors
T2 - A Prospective Multicenter Cohort Study
AU - Japanese Musculoskeletal Oncology Group (JMOG)
AU - Iwata, Shintaro
AU - Kawai, Akira
AU - Ueda, Takafumi
AU - Ishii, Takeshi
AU - Yonemoto, Tsukasa
AU - Kamoda, Hiroto
AU - Suzuki, Yoshihisa
AU - Kikuta, Kazutaka
AU - Imanishi, Jungo
AU - Okubo, Taketo
AU - Yazawa, Yasuo
AU - Sotobori, Tsukasa
AU - Murata, Hiroaki
AU - Ozaki, Toshifumi
AU - Kunisada, Toshiyuki
AU - Fujiwara, Tomohiro
AU - Kakunaga, Shigeki
AU - Hiraoka, Koji
AU - Hamada, Tetsuya
AU - Matsuda, Kotaro
AU - Yanagawa, Takashi
AU - Saito, Kenichi
AU - Namba, Hirofumi
AU - Kawasaki, Motohiro
AU - Nishimura, Shunji
AU - Hashimoto, Kazuhiko
AU - Okamoto, Takeshi
AU - Anazawa, Ukei
AU - Watanabe, Itsuo
AU - Hakozaki, Michiyuki
AU - Imura, Yoshinori
AU - Takenaka, Satoshi
AU - Kobayashi, Eisuke
AU - Ogura, Koichi
AU - Yasuda, Taketoshi
AU - Suzuki, Kayo
AU - Akiyama, Toru
AU - Hosaka, Masami
AU - Watanuki, Munenori
AU - Hayashi, Kou
AU - Shirai, Toshiharu
AU - Terauchi, Ryu
AU - Aiba, Hisaki
AU - Kimura, Hiroaki
AU - Asanuma, Kunihiro
AU - Nakamura, Tomoki
AU - Hagi, Tomohito
AU - Abe, Satoshi
AU - Sato, Kenji
AU - Yoshida, Yukihiro
N1 - Funding Information:
The authors thank Ms Misa Monju for her great support in organizing the Japanese Musculoskeletal Oncology Group. Collaborators and affiliations Chiba Cancer Center: Tsukasa Yonemoto, Hiroto Kamoda; Tachikawa Hospital: Yoshihisa Suzuki, Kazutaka Kikuta; Saitama Medical University International Medical Center: Jungo Imanishi, Taketo Okubo, Yasuo Yazawa; Osaka International Cancer Institute: Tsukasa Sotobori; Matsushita Memorial Hospital: Hiroaki Murata; Okayama University: Toshifumi Ozaki, Toshiyuki Kunisada, Tomohiro Fujiwara; National Hospital Organization Osaka National Hospital: Shigeki Kakunaga; Kurume University; Koji Hiraoka, Tetsuya Hamada, Kotaro Matsuda; Gunma University; Takashi Yanagawa, Kenichi Saito; Kochi University; Hirofumi Namba, Motohiro Kawasaki; Kindai University: Shunji Nishimura, Kazuhiko Hashimoto; Kyoto University: Takeshi Okamoto; Tokyo Dental College Ichikawa General Hospital: Ukei Anazawa, Itsuo Watanabe; Fukushima Medical University; Michiyuki Hakozaki; Osaka University: Yoshinori Imura, Satoshi Takenaka; National Cancer Center Hospital: Eisuke Kobayashi, Koichi Ogura; University of Toyama: Taketoshi Yasuda, Kayo Suzuki; Jichi Medical University Saitama Medical Center: Toru Akiyama; Tohoku University: Masami Hosaka, Munenori Watanuki, Kou Hayashi; Kyoto Prefectural University of Medicine: Toshiharu Shirai, Ryu Terauchi; Nagoya City University: Hisaki Aiba, Hiroaki Kimura; Mie University: Kunihiro Asanuma, Tomoki Nakamura, Tomohito Hagi; Teikyo University: Satoshi Abe, Kenji Sato; Nihon University: Yukihiro Yoshida; Juntendo University: Yoshiyuki Suehara, Keisuke Akaike; National Hospital Organization Hokkaido Cancer Center: Hiroaki Hiraga, Tamotsu Soma; The University of Tokyo: Hiroshi Kobayashi, Yusuke Shinoda, Ryoko Sawada.
Publisher Copyright:
© 2020, Society of Surgical Oncology.
PY - 2021/7
Y1 - 2021/7
N2 - Background: A prospective cohort study was conducted to determine the incidence and risk factors of symptomatic venous thromboembolism (sVTE) during the perioperative period in patients with malignant bone and soft tissue tumors. Methods: Patients with newly diagnosed primary malignant bone and soft tissue tumors for whom definitive surgery was planned were consecutively registered among 27 tertiary hospitals specializing in musculoskeletal oncology. Clinicopathological information on each patient was collected prospectively, and careful follow-up was conducted for 6 months after surgery. The study endpoint was the occurrence of sVTE, including deep vein thrombosis (DVT) and pulmonary embolism (PE). Results: Eleven of 929 patients developed sVTE, including 8 patients with DVT, 2 with PE, and 1 with both, making the incidence of sVTE 1.18%. The median time until the development of sVTE after tumor resection was 11 days, ranging from − 7 to 95 days. Multiple logistic regression analyses revealed that ischemic heart disease as a comorbidity, maximum tumor diameter exceeding 8 cm, and elevated preoperative platelet count were independent risk factors for sVTE. Conclusions: The incidence of sVTE in this series of patients with bone and soft tissue sarcomas was 1.18%, which was relatively lower than in previous retrospective studies. We identified the risk factors for sVTE specific to patients with malignant bone and soft tissue tumors, and these included ischemic heart disease, tumor size, and elevation of the preoperative platelet count.
AB - Background: A prospective cohort study was conducted to determine the incidence and risk factors of symptomatic venous thromboembolism (sVTE) during the perioperative period in patients with malignant bone and soft tissue tumors. Methods: Patients with newly diagnosed primary malignant bone and soft tissue tumors for whom definitive surgery was planned were consecutively registered among 27 tertiary hospitals specializing in musculoskeletal oncology. Clinicopathological information on each patient was collected prospectively, and careful follow-up was conducted for 6 months after surgery. The study endpoint was the occurrence of sVTE, including deep vein thrombosis (DVT) and pulmonary embolism (PE). Results: Eleven of 929 patients developed sVTE, including 8 patients with DVT, 2 with PE, and 1 with both, making the incidence of sVTE 1.18%. The median time until the development of sVTE after tumor resection was 11 days, ranging from − 7 to 95 days. Multiple logistic regression analyses revealed that ischemic heart disease as a comorbidity, maximum tumor diameter exceeding 8 cm, and elevated preoperative platelet count were independent risk factors for sVTE. Conclusions: The incidence of sVTE in this series of patients with bone and soft tissue sarcomas was 1.18%, which was relatively lower than in previous retrospective studies. We identified the risk factors for sVTE specific to patients with malignant bone and soft tissue tumors, and these included ischemic heart disease, tumor size, and elevation of the preoperative platelet count.
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U2 - 10.1245/s10434-020-09308-6
DO - 10.1245/s10434-020-09308-6
M3 - Article
C2 - 33165723
AN - SCOPUS:85095724289
SN - 1068-9265
VL - 28
SP - 3919
EP - 3927
JO - Annals of Surgical Oncology
JF - Annals of Surgical Oncology
IS - 7
ER -