TY - JOUR
T1 - Identification of risk factors for venous thromboembolism and validation of the Khorana score in patients with advanced lung cancer
T2 - based on the multicenter, prospective Rising-VTE/NEJ037 study data
AU - Tsubata, Yukari
AU - Kawakado, Keita
AU - Hamai, Kosuke
AU - Furuya, Naoki
AU - Yokoyama, Toshihide
AU - Saito, Ryota
AU - Nakamura, Atsushi
AU - Masuda, Takeshi
AU - Hamaguchi, Megumi
AU - Kuyama, Shoichi
AU - Honda, Ryoichi
AU - Senoo, Tadashi
AU - Nakanishi, Masamoto
AU - Hotta, Takamasa
AU - Yamasaki, Masahiro
AU - Ishikawa, Nobuhisa
AU - Fujitaka, Kazunori
AU - Kubota, Tetsuya
AU - Kobayashi, Kunihiko
AU - Isobe, Takeshi
N1 - Funding Information:
This work was funded by Daiichi Sankyo Co., Ltd. [LIX-MD-15003]. Daiichi Sankyo Co., Ltd. only provided the research funds and was not involved in protocol planning or preparation, study progress management, data collection, and statistical analysis.
Publisher Copyright:
© 2022, The Author(s).
PY - 2023/1
Y1 - 2023/1
N2 - Background: Management of cancer-associated venous thromboembolism (VTE) is essential in cancer treatment selection and prognosis. However, currently, no method exists for assessing VTE risk associated with advanced lung cancer. Therefore, we assessed VTE risk, including driver gene mutation, in advanced lung cancer and performed a Khorana score validation. Methods: The Rising-VTE/NEJ037 study was a multicenter prospective observational study that included patients with advanced lung cancer. In the Rising-VTE/NEJ037 study, the Khorana score was calculated for enrolled patients with available data on all Khorana score components. The modified Khorana score was based on the body mass index of ≥ 25 kg/m2, according to the Japanese obesity standard. A multivariate logistic regression analysis, including patient background characteristics, was performed to evaluate the presence of VTE 2 years after the lung cancer diagnosis. Results: This study included 1008 patients with lung cancer, of whom 100 (9.9%) developed VTE. From the receiver operating characteristic curve analysis, VTE risk could not be determined because both the Khorana score (0.518) and modified Khorana score (0.516) showed very low areas under the curve. The risk factors for VTE in the multivariate analysis included female sex, adenocarcinoma, performance status, N factor, lymphocyte count, platelet count, prothrombin fragment 1 + 2 and diastolic blood pressure. Conclusion: The Khorana score, which is widely used in cancer-VTE risk assessment, was less useful for Japanese patients with advanced lung cancer. Prothrombin fragment 1 + 2, a serum marker involved in coagulation, was more suitable for risk identification. Clinical trial information: jRCTs061180025.
AB - Background: Management of cancer-associated venous thromboembolism (VTE) is essential in cancer treatment selection and prognosis. However, currently, no method exists for assessing VTE risk associated with advanced lung cancer. Therefore, we assessed VTE risk, including driver gene mutation, in advanced lung cancer and performed a Khorana score validation. Methods: The Rising-VTE/NEJ037 study was a multicenter prospective observational study that included patients with advanced lung cancer. In the Rising-VTE/NEJ037 study, the Khorana score was calculated for enrolled patients with available data on all Khorana score components. The modified Khorana score was based on the body mass index of ≥ 25 kg/m2, according to the Japanese obesity standard. A multivariate logistic regression analysis, including patient background characteristics, was performed to evaluate the presence of VTE 2 years after the lung cancer diagnosis. Results: This study included 1008 patients with lung cancer, of whom 100 (9.9%) developed VTE. From the receiver operating characteristic curve analysis, VTE risk could not be determined because both the Khorana score (0.518) and modified Khorana score (0.516) showed very low areas under the curve. The risk factors for VTE in the multivariate analysis included female sex, adenocarcinoma, performance status, N factor, lymphocyte count, platelet count, prothrombin fragment 1 + 2 and diastolic blood pressure. Conclusion: The Khorana score, which is widely used in cancer-VTE risk assessment, was less useful for Japanese patients with advanced lung cancer. Prothrombin fragment 1 + 2, a serum marker involved in coagulation, was more suitable for risk identification. Clinical trial information: jRCTs061180025.
KW - Deep vein thrombosis
KW - Khorana score
KW - Lung cancer
KW - Prothrombin fragment 1 + 2
KW - Pulmonary thromboembolism
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U2 - 10.1007/s10147-022-02257-y
DO - 10.1007/s10147-022-02257-y
M3 - Article
C2 - 36357710
AN - SCOPUS:85141714909
SN - 1341-9625
VL - 28
SP - 69
EP - 78
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 1
ER -