Systematic Review Registration: https://www.crd.york.ac.uk/prospero/, identifier CRD420251218825.With changes in human lifestyles and behavioral patterns, cancer has become one of the leading diseases threatening global public health. During chemotherapy, the strong irritant properties of antineoplastic agents may cause tissue and organ damage or result in drug extravasation. The use of central venous catheter (CVC) allows the safe administration of chemotherapeutic agents and effectively reduces the risk of local tissue injury and extravasation. To ensure the continuous delivery of chemotherapy, parenteral nutrition, or blood transfusion, patients with malignancies often require long-term CVC placement.Common types of CVC include peripherally inserted central catheter (PICC), tunneled central venous catheters, and totally implantable venous access ports (Ports). However, Catheter Related Thrombosis (CRT), as one of the common complications after central venous catheterization, has become an important factor affecting the continuity of treatment and clinical efficacy of cancer patients. Studies have shown that the average incidence of CVCrelated thrombosis in cancer patients is about 5%-20%, and there is a certain mortality (CLOTS Trials Collaboration, 2014;Zhang et al., 2018), which is one of the risk factors leading to the death of cancer patients (Farge et al., 2016). Thrombotic events can increase the risk of disability, prolong hospitalization, interrupt intravenous chemotherapy, and exacerbate disease burden, thereby shortening patient survival and imposing substantial economic costs. CRT may also lead to catheter dysfunction, increased susceptibility to infection, and treatment interruption. In rare cases, it can result in post-thrombotic syndrome, cause further venous damage, or trigger life-threatening complications such as pulmonary embolism (PE), ultimately endangering patient survival (Geerts et al., 2004;Langer and Bokemeyer, 2012).Prophylactic anticoagulation has been proposed as an effective strategy to reduce the incidence of CVC-related thrombosis by inhibiting the coagulation cascade and decreasing thrombus formation around the catheter (Khorana, 2013;Mosarla et al., 2019). However, current guidelines still have different recommendations on preventive anticoagulation for CVC-related thrombosis in cancer patients. The Chinese Guidelines for the Prevention and Treatment of Thrombotic Diseases (Chinese Thrombosis Guidelines Expert Committee, 2018) recommend venous thromboembolism risk assessment for patients with central venous catheter. For patients with moderate or high risk and without anticoagulation contraindications, it is recommended to use low-molecular-weight heparin (LMWH) or edoxaban for CRT prevention. The American Society of Clinical Oncology (ASCO) (Lyman et al., 2015) advises prophylactic-dose LMWH, unfractionated heparin, or rivaroxaban for patients with a Khorana score ≥3 or those with pancreatic, lung, or gastric cancer. In contrast, the European Society for Medical Oncology (ESMO) (Falanga et al., 2023) and the American Society of Hematology (ASH) (Lyman et al., 2021) do not recommend the use of drugs to prevent CRT. The above situation indicates that there is still a lack of sufficient research evidence to support the clinical application of prophylactic anticoagulants and reach a consensus in guidelines. Therefore, more evidence is needed to support whether CRT prevention is necessary and which prevention strategy is safer and more effective (to maintain the balance between the efficacy of thrombosis prevention and the risk of bleeding, and to increase the benefit of patients).In this context, systematically reviewing the research progress and evidence gaps in this field is of great value. Bibliometric analysis can systematically map the research landscape, evolutionary trends and research hotspots in the field of prophylaxis for central venous catheter-related thrombosis in cancer patients; it not only clarifies the characteristic shift of mainstream anticoagulant strategies from traditional agents (warfarin, LMWH) to direct oral anticoagulants (DOACs) in this field, but also identifies the current evidence gaps and controversial issues lacking comprehensive quantitative comparison of multiple interventions. This provides a clear theoretical basis and research direction for the subsequent conduct of network meta-analysis, rendering the selection of interventions, setting of outcome indicators and determination of research priorities in the network meta-analysis more targeted and evidence-based. Network meta-analysis, on the other hand, can integrate both direct and indirect comparison evidence, quantitatively evaluating the differences in efficacy and safety among various prophylactic anticoagulation strategies. Therefore, this study intends to use bibliometric methods to analyze the landscape and development trajectory of CVC-related thrombosis anticoagulation in cancer patients, and to apply Bayesian network meta-analysis to comprehensively evaluate the efficacy and safety of different anticoagulants in preventing CRT. The aim is to provide evidence-based support for prophylactic anticoagulation decisionmaking, improve cancer patient prognosis, and offer future research directions in the field of CVC-related thrombosis anticoagulation.The current study follows the PRISMA statement (Page et al., 2021) (Supplementary Table S1), The complete study protocol was pre-registered at PROSPERO with the registration number CRD420251218825. As no personal patient information is involved, ethical approval is not required for this study.The Web of Science Core Collection database was searched, with the citation index set to Science Citation Index Expanded (SCI-Expanded), to construct the search strategy for CVC-related thrombosis prevention and treatment in cancer patients. All relevant literature from 2000 to 16 April 2025, was retrieved, limited to "Article" and "Review article" types, and restricted to English language. The search strategy is detailed in Supplementary Table S2.Search the PubMed, The Cochrane Library, Embase and Web of Science databases. The search time range extended from database inception to 28 May 2025. The search focused on clinical studies regarding prophylactic anticoagulation for CVC-related thrombosis in cancer patients, with no language restrictions. The search included keywords such as "anticoagulation," "central venous catheter", and "cancer." Additional keywords were derived by reviewing relevant literature appendices, and a combined approach of subject terms and free terms was used to construct the search strategy. The detailed search strategy is provided in Supplementary Table S3.The bibliometric analysis was conducted using the Web of Science (WoS) Core Collection, a widely regarded and standardized source for bibliometric data. WoS provides consistent metadata, such as citation counts, author affiliations, and indexed keywords, essential for constructing co-authorship networks, co-citation maps, and keyword co-occurrence analyses. These features make WoS an ideal choice for bibliometric mapping. Owing to the inherent functional limitations of bibliometric analysis software, which only support single-database operations, the bibliometric component of this study exclusively included the WoS Core Collection.The inclusion criteria for this study were as follows: (1) study population: Patients with malignancies who have undergone CVC (Central Venous Catheter) placement, aged ≥18 years, and received prophylactic anticoagulation during CVC placement. The tumor types include both hematologic and solid tumors; (2) interventions: All prophylactic anticoagulants were included in the search. The DOACs mainly included rivaroxaban, apixaban, edoxaban, and dabigatran; low molecular weight heparins (LMWH) included enoxaparin, dalteparin, nadroparin, etc.; vitamin K antagonists (VKAs) included warfarin and other coumarin and indanedione derivatives; (3) outcomes: The primary outcomes were venous thromboembolism (VTE) and major bleeding events. The secondary outcomes included all bleeding events, all-cause mortality events, and adverse events. VTE was defined as a composite of pulmonary embolism (PE) and deep venous thrombosis (DVT), including both symptomatic and asymptomatic cases. The occurrence of CRT must be confirmed through diagnostic methods. PE diagnosis included computed tomography (CT), D-dimer, CT pulmonary angiography, and ventilation/perfusion scanning. Diagnosis of symptomatic or asymptomatic DVT included color Doppler ultrasound, venography, D-dimer, CT venography, magnetic resonance venography, radioactive iodine fibrinogen uptake test, and impedance plethysmography. Major bleeding events, bleeding events, and adverse events were defined according to the standards of each study (bleeding events encompass all bleeding conditions, including major bleeding; adverse events included any non-bleeding adverse events). Death was defined as all-cause mortality, including both catheter-related thrombosis-related death and death due to cancer progression; (4) study types: randomized controlled trials (RCTs) or non-randomized controlled trials (Non-RCTs). Non-RCTs primarily included non-randomized concurrent controlled trials, self-controlled studies, controlled studies, criteria (1) research such as (2) (3) (4) study types, such as and studies with or the studies, and the information according to the inclusion studies were using by on and and were to study there were between the a be to the The to be from the included studies study study interventions, and of and outcome risk of for the included studies was according to the of controlled trials The risk of for was using the Cochrane of with in the selection of the each study according to the For each the risk of was as or were through and a risk of was using study used the in to analysis of relevant including and citation and maps, and were analysis was conducted using software, and co-occurrence and were and was used to et al., network meta-analysis was exclusively using the in a used for network meta-analysis the Bayesian For with were as the The of was using and a was between an was Bayesian was using the with the used for to the of and the for were used for each The in the Bayesian and were to the and were using and the In the of were to the between direct and indirect with analysis conducted using the of each different outcome the in was used for were this the to complete and the were and were This was used for and the of this study were mainly derived on the Bayesian analysis from the The of each was to the of each The the was and of indicates the a of indicates the was to the for all more clinical trials were was using to the and this to CVC-related thrombosis prevention and treatment in cancer patients were and from the Web of with an of the bibliometric shown in Supplementary the search from all a of were for the network All were for and after the studies and those with study types were after studies were included et al., et al., et al., et al., et al., et al., et al., et al., et al., et al., et al., et al., et al., et al., et al., et al., et al., et al., et al., The study is shown in Supplementary of clinical studies were included in the network of which 16 were and were of cancer patients who CVC were The was the no prophylaxis studies, prophylactic CVCrelated thrombosis were ultimately of the included studies was using the Cochrane of and the In the assessment the risk of for was as study et al., was a risk of other due to a of study drug which was mainly by clinical during chemotherapy, the was and no on the primary study study et al., was as for other to a diagnosis of the primary outcome (CRT), the diagnosis was consistent all and not a on the study The studies were as or for each on whether the relevant the included studies an the were and the studies confirmed that the no on the study The for and Non-RCTs shown in Supplementary of in the field of CVC-related thrombosis prevention and treatment in cancer patients is shown in The a with in and in in by a in the The number of in with the from the to this research in the field of CVC-related thrombosis prevention and treatment in cancer patients analysis of the by (Supplementary Table that the in both and citation and and The that the was more to with other The analysis shown in on CVC-related thrombosis in cancer patients were mainly in and The in that the has the with other with the and is an in of and have in research on CVC-related thrombosis prevention and treatment in cancer patients, including Supplementary provide on the and with the number of The with the was in The were in primarily focused on and Supplementary Table the by The with the and citation were Thrombosis and Cochrane of Systematic the to the in the Citation with the of Oncology that the citation of is more to both the factor and Cochrane of Systematic is the in this To the citation and of and the subject of a analysis of was using As shown in the the primary that research in molecular and is by research in and clinical studies, the development analysis of (Supplementary Table that the was a clinical study by from in in et al., which has been in this field primarily on the with CVC in cancer keyword co-occurrence can the of and trends in the field of CVC-related thrombosis prevention and treatment in cancer patients. 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This result indicates that DOACs have clinical application and research the of DOACs by the network meta-analysis in this study is consistent with the characteristic shift of research hotspots DOACs in the bibliometric This further the clinical application of DOACs in the prophylaxis of central venous catheter-related thrombosis in cancer patients and provides a solid basis for the research hotspots by the bibliometric study is the to apply Bayesian network analysis to evaluate the safety and efficacy of different prophylactic strategies for CVC-related thrombosis in cancer patients. 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Mingyu Meng
Qimeng Xu
Shiran Qin
Frontiers in Pharmacology
Guangxi Medical University
The People's Hospital of Guangxi Zhuang Autonomous Region
Zhuzhou Central Hospital
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Meng et al. (Mon,) studied this question.
www.synapsesocial.com/papers/69fd7cd4bfa21ec5bbf05ab6 — DOI: https://doi.org/10.3389/fphar.2026.1863333
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