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      Incidence of venous thromboembolism in advanced lung cancer and efficacy and safety of direct oral anticoagulants: a multicenter, prospective, observational study (Rising-VTE/NEJ037 study)

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          Abstract

          Background:

          Venous thromboembolism (VTE) is a well-known type of cancer-associated thrombosis and a common complication of malignancy. However, the incidence of VTE associated with lung cancer and the effectiveness of direct oral anticoagulants remain unclear. This study aimed to identify the incidence of VTE associated with lung cancer at the time of diagnosis or during treatment, the efficacy and safety of edoxaban, and associated risk factors.

          Methods:

          The Rising-VTE/NEJ037 study was a multicenter prospective observational study. Altogether, 1021 patients with lung cancer who were unsuitable for radical resection or radiation were enrolled and followed up for 2 years. Patients with VTE at the time of lung cancer diagnosis started treatment with edoxaban. The primary endpoint of this trial was the rate of newly diagnosed VTE after enrollment or recurrence rate 6 months after treatment initiation.

          Results:

          Data were available for 1008 patients. The median age was 70 years (range: 30–94 years), and 70.8% were men. Sixty-two patients had VTE at the time of lung cancer diagnosis, and 38 (9.9%) developed VTE at follow-up. No cases of VTE recurrence were recorded 6 months after treatment initiation with edoxaban. Major and clinically relevant non-major bleeding events occurred in 4.9% of patients and increased to 22.7% in the edoxaban treatment group.

          Conclusions:

          VTE occurrence should be monitored during lung cancer treatment. Although treatment with edoxaban was highly effective in preventing VTE recurrence, its administration should be cautiously considered because of the high bleeding rate.

          Trial registration:

          jRCTs061180025.

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          Most cited references23

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          Venous Thromboembolism Prophylaxis and Treatment in Patients With Cancer: ASCO Clinical Practice Guideline Update

          PURPOSE To provide updated recommendations about prophylaxis and treatment of venous thromboembolism (VTE) in patients with cancer. METHODS PubMed and the Cochrane Library were searched for randomized controlled trials (RCTs) and meta-analyses of RCTs published from August 1, 2014, through December 4, 2018. ASCO convened an Expert Panel to review the evidence and revise previous recommendations as needed. RESULTS The systematic review included 35 publications on VTE prophylaxis and treatment and 18 publications on VTE risk assessment. Two RCTs of direct oral anticoagulants (DOACs) for the treatment of VTE in patients with cancer reported that edoxaban and rivaroxaban are effective but are linked with a higher risk of bleeding compared with low-molecular-weight heparin (LMWH) in patients with GI and potentially genitourinary cancers. Two additional RCTs reported on DOACs for thromboprophylaxis in ambulatory patients with cancer at increased risk of VTE. RECOMMENDATIONS Changes to previous recommendations: Clinicians may offer thromboprophylaxis with apixaban, rivaroxaban, or LMWH to selected high-risk outpatients with cancer; rivaroxaban and edoxaban have been added as options for VTE treatment; patients with brain metastases are now addressed in the VTE treatment section; and the recommendation regarding long-term postoperative LMWH has been expanded. Re-affirmed recommendations: Most hospitalized patients with cancer and an acute medical condition require thromboprophylaxis throughout hospitalization. Thromboprophylaxis is not routinely recommended for all outpatients with cancer. Patients undergoing major cancer surgery should receive prophylaxis starting before surgery and continuing for at least 7 to 10 days. Patients with cancer should be periodically assessed for VTE risk, and oncology professionals should provide patient education about the signs and symptoms of VTE. Additional information is available at www.asco.org/supportive-care-guidelines .
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            Prognosis of cancers associated with venous thromboembolism.

            Little is known about the prognosis of cancer discovered during or after an episode of venous thromboembolism. We linked the Danish National Registry of Patients, the Danish Cancer Registry, and the Danish Mortality Files to obtain data on the survival of patients who received a diagnosis of cancer at the same time as or after an episode of venous thromboembolism. Their survival was compared with that of patients with cancer who did not have venous thromboembolism (control patients), who were matched in terms of type of cancer, age, sex, and year of diagnosis. Of 668 patients who had cancer at the time of an episode of deep venous thromboembolism, 44.0 percent of those with data on the spread of disease (563 patients) had distant metastasis, as compared with 35.1 percent of 5371 control patients with data on spread (prevalence ratio, 1.26; 95 percent confidence interval, 1.13 to 1.40). In the group with cancer at the time of venous thromboembolism, the one-year survival rate was 12 percent, as compared with 36 percent in the control group (P<0.001), and the mortality ratio for the entire follow-up period was 2.20 (95 percent confidence interval, 2.05 to 2.40). Patients in whom cancer was diagnosed within one year after an episode of venous thromboembolism had a slightly increased risk of distant metastasis at the time of the diagnosis (prevalence ratio, 1.23 [95 percent confidence interval, 1.08 to 1.40]) and a relatively low rate of survival at one year (38 percent, vs. 47 percent in the control group; P<0.001). Cancer diagnosed at the same time as or within one year after an episode of venous thromboembolism is associated with an advanced stage of cancer and a poor prognosis.
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              Edoxaban for the Treatment of Cancer-Associated Venous Thromboembolism

              Low-molecular-weight heparin is the standard treatment for cancer-associated venous thromboembolism. The role of treatment with direct oral anticoagulant agents is unclear.
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                Author and article information

                Contributors
                Role: ConceptualizationRole: Data curationRole: InvestigationRole: MethodologyRole: Writing original draftRole: Writing review editing
                Role: Data curationRole: InvestigationRole: MethodologyRole: Writing review editing
                Role: InvestigationRole: Writing review editing
                Role: InvestigationRole: Writing review editing
                Role: InvestigationRole: Writing review editing
                Role: InvestigationRole: Writing review editing
                Role: InvestigationRole: Writing review editing
                Role: InvestigationRole: Writing review editing
                Role: InvestigationRole: Writing review editing
                Role: InvestigationRole: Writing review editing
                Role: InvestigationRole: Writing review editing
                Role: InvestigationRole: Writing review editing
                Role: InvestigationRole: Writing review editing
                Role: InvestigationRole: MethodologyRole: Writing review editing
                Role: InvestigationRole: MethodologyRole: Writing review editing
                Role: InvestigationRole: MethodologyRole: Writing review editing
                Role: InvestigationRole: MethodologyRole: Writing review editing
                Role: Data curationRole: Formal analysisRole: Writing review editing
                Role: InvestigationRole: MethodologyRole: Writing review editing
                Role: ConceptualizationRole: SupervisionRole: Writing review editing
                Journal
                Ther Adv Med Oncol
                Ther Adv Med Oncol
                TAM
                sptam
                Therapeutic Advances in Medical Oncology
                SAGE Publications (Sage UK: London, England )
                1758-8340
                1758-8359
                21 July 2022
                2022
                : 14
                : 17588359221110171
                Affiliations
                [1-17588359221110171]Department of Internal Medicine, Division of Medical Oncology and Respiratory Medicine, Shimane University Faculty of Medicine, 89-1 Enya-cho, Izumo, Shimane 693-8501, Japan
                [2-17588359221110171]Department of Internal Medicine, Division of Medical Oncology and Respiratory Medicine, Shimane University Faculty of Medicine, Izumo, Shimane, Japan
                [3-17588359221110171]Department of Respiratory Medicine, Hiroshima Prefectural Hospital, Minami-ku, Hiroshima, Japan
                [4-17588359221110171]Division of Respiratory Medicine, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan
                [5-17588359221110171]Department of Respiratory Medicine, Kurashiki Central Hospital, Kurashiki, Okayama, Japan
                [6-17588359221110171]Department of Respiratory Medicine, Tohoku University, Sendai, Miyagi, Japan
                [7-17588359221110171]Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan
                [8-17588359221110171]Department of Respiratory Medicine, Hiroshima University Hospital, Minami-ku, Hirosima, Japan
                [9-17588359221110171]Department of Internal Medicine, Division of Medical Oncology and Respiratory Medicine, Shimane University Faculty of Medicine, Izumo, Shimane, Japan
                [10-17588359221110171]Department of Respiratory Medicine, Iwakuni Clinical Center, Iwakuni, Yamaguchi, Japan
                [11-17588359221110171]Department of Respiratory Medicine, Asahi General Hospital, Asahi, Chiba, Japan
                [12-17588359221110171]Department of Respiratory Medicine, National Hospital Organization, Kure Medical Center, Kure, Hiroshima, Japan
                [13-17588359221110171]Department of Medical Oncology, Yamaguchi-Ube Medical Center, Ube, Yamaguchi, Japan
                [14-17588359221110171]Department of Respiratory Disease, Hiroshima Red Cross Hospital and Atomic-bomb Survivors Hospital, Naka-ku, Hiroshima, Japan
                [15-17588359221110171]Department of Respiratory Medicine, Hiroshima Prefectural Hospital, Minami-ku, Hiroshima, Japan
                [16-17588359221110171]Department of Respiratory Medicine, Hiroshima University Hospital, Minami-ku, Hirosima, Japan
                [17-17588359221110171]Department of Respiratory Medicine and Allergology, Kochi University Hospital, Nankoku, Kochi, Japan
                [18-17588359221110171]Department of Data Science, Center for Clinical Sciences, National Center for Global Health and Medicine, Shinjuku-ku, Tokyo, Japan
                [19-17588359221110171]Department of Pulmonary Medicine, Saitama Medical University International Medical Center, Hidaka, Saitama, Japan
                [20-17588359221110171]Department of Internal Medicine, Division of Medical Oncology and Respiratory Medicine, Shimane University Faculty of Medicine, Izumo, Shimane, Japan
                Author notes
                Author information
                https://orcid.org/0000-0002-4260-2849
                https://orcid.org/0000-0003-3261-8828
                Article
                10.1177_17588359221110171
                10.1177/17588359221110171
                9310216
                35898966
                0bf72ea3-d205-4bf4-9f83-3fd7215206aa
                © The Author(s), 2022

                This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License ( https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page ( https://us.sagepub.com/en-us/nam/open-access-at-sage).

                History
                : 9 April 2022
                : 9 June 2022
                Funding
                Funded by: Daiichi-Sankyo, FundRef https://doi.org/10.13039/501100002973;
                Award ID: LIX-MD-15003
                Categories
                Original Research
                Custom metadata
                January-December 2022
                ts1

                anticoagulants,cancer,lung neoplasms,pulmonary embolism,venous thromboembolism,venous thrombosis

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