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Natural history of cancer-associated splanchnic vein thrombosis
Author(s): ,
Ang Li
Affiliations:
Section of Hematology and Oncology, Baylor College of Medicine, Houston, Texas, USA
Ang Li, Section of Hematology and Oncology, Baylor College of Medicine, One Baylor Plaza, 011DF, Houston, TX 77030, USA.
,
Shengling Ma
Affiliations:
Section of Hematology and Oncology, Baylor College of Medicine, Houston, Texas, USA
,
Raka Bandyo
Affiliations:
Harris Health System, Houston, Texas, USA
,
Francisco Novoa
Affiliations:
Washington University School of Medicine in St. Louis, St. Louis, Missouri, USA
,
Danielle Guffey
Affiliations:
Institute for Clinical and Translational Research, Baylor College of Medicine, Houston, Texas, USA
,
Jun Y. Jiang
Affiliations:
Section of Hematology and Oncology, Baylor College of Medicine, Houston, Texas, USA
Hanqing Shang
Affiliations:
Department of Medicine, Baylor College of Medicine, Houston, Texas, USA
ISTH Academy. Li A. 05/01/24; 422465
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Journal Abstract
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Background

There is uncertainty in the management of cancer-associated isolated splanchnic vein thrombosis (SpVT).

Objectives

To describe the natural history of SpVT by cancer type and thrombus composition and to review anticoagulation (AC) practices and associated rates of usual-site venous thromboembolism (VTE), major and clinically relevant nonmajor bleeding (MB/CRNMB), recanalization/progression, and mortality.

Methods

We performed a retrospective cohort study in patients with SpVT at 2 cancer care centers in Houston, Texas. We estimated the incidence of usual-site VTE and MB/CRNMB at 6 months using competing risk methods and examined venous patency in a subset of patients with repeat imaging. We assessed associations with mortality using Cox regression.

Results

Among 15 342 patients with an incident cancer diagnosis from 2011 to 2020, we identified 298 with isolated SpVT. Patients with hepatocellular carcinoma (HCC) and SpVT (n = 146) had the highest disease prevalence (20%), lowest rate of AC treatment (2%), and similar rate of usual-site VTE (4.2%) vs those without SpVT (5.2%) at 6 months, though tumor thrombus vs bland was associated with worse overall survival. In patients with non-HCC bland SpVT (n = 114), AC (n = 37) was more common in those with non-upper gastrointestinal cancers and fewer comorbidities. AC was associated with more recanalization (44% vs 15%, P = .041) but no differences in usual-site VTE, MB/CRNMB, or mortality at 6 months.

Conclusion

Cancer-associated isolated SpVT is a common but heterogeneous thrombotic disease that is treated differently from usual-site VTE. Tumor thrombus is a negative prognostic factor. Initiation of AC in bland thrombi requires judicious consideration of thrombotic and bleeding risk.

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