# Prolonged Edoxaban in Patients With Low Body Weight and Cancer-Associated Isolated Distal Deep Vein Thrombosis

**Authors:** Tomoyuki Nagai, Naohiko Nakanishi, Yugo Yamashita, Takeshi Morimoto, Nao Muraoka, Michihisa Umetsu, Yuji Nishimoto, Takuma Takada, Yoshito Ogihara, Tatsuya Nishikawa, Nobutaka Ikeda, Kazunori Otsui, Daisuke Sueta, Yukari Tsubata, Masaaki Shoji, Ayumi Shikama, Yutaka Hosoi, Yasuhiro Tanabe, Ryuki Chatani, Kengo Tsukahara, Kitae Kim, Satoshi Ikeda, Takeshi Kimura, Satoaki Matoba

PMC · DOI: 10.1016/j.jacadv.2025.101956 · JACC: Advances · 2025-07-04

## TL;DR

A 12-month treatment with edoxaban is more effective than a 3-month treatment for preventing blood clots in cancer patients with low body weight.

## Contribution

This study shows prolonged edoxaban treatment is effective for low-weight cancer patients with isolated distal DVT without increasing bleeding risk.

## Key findings

- 12-month edoxaban reduced thrombotic events in low-weight patients compared to 3-month treatment.
- Bleeding risk remained similar in low-weight patients with 12-month treatment.
- Non-low weight patients had increased bleeding risk with 12-month treatment.

## Abstract

The ONCO DVT study revealed that 12-month edoxaban treatment for cancer-associated isolated distal deep vein thrombosis (IDDVT) was superior to 3-month edoxaban treatment. However, the influence of body weight on efficacy and safety remains unknown.

We compared 12-month and 3-month edoxaban treatments in patients with low body weight and cancer-associated IDDVT.

In this prespecified subgroup analysis of the ONCO DVT study, we divided patients by body weight with a 60 kg cutoff. The primary endpoint was symptomatic recurrent venous thromboembolism or venous thromboembolism-related death at 12 months.

Of the 601 participants, 426 had low body weight, 99% receiving a reduced dose of edoxaban. The 1-year primary endpoint rate was significantly lower in the 12-month edoxaban group than in the 3-month group in both the low body weight (1.0% vs 6.2%, P = 0.003; OR: 0.15; 95% CI: 0.02-0.55) and the non-low body weight (1.0% vs 10.0%, P = 0.005; OR: 0.10; 95% CI: 0.01-0.54) subgroups. The 1-year major bleeding rate was not different between the 12-month and 3-month groups in the low body weight subgroup (7.0% vs 8.4%, P = 0.57), whereas in the non-low body weight subgroup, it was significantly higher in the 12-month edoxaban group than in the 3-month edoxaban group (14.7% vs 3.8%, P = 0.01).

Twelve-month edoxaban treatment in cancer-associated IDDVT was superior to 3-month edoxaban treatment in terms of thrombotic events without increased bleeding risk among patients with low body weight but with increased bleeding risk among patients with non-low body weight.

## Linked entities

- **Chemicals:** edoxaban (PubChem CID 10280735)
- **Diseases:** cancer (MONDO:0004992), venous thromboembolism (MONDO:0005399)

## Full-text entities

- **Diseases:** bleeding (MESH:D006470), venous thromboembolism (MESH:D054556), Deep Vein Thrombosis (MESH:D020246), DVT (OMIM:612862), thrombotic (MESH:D013927), Cancer (MESH:D009369), death (MESH:D003643)
- **Chemicals:** Edoxaban (MESH:C552171)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12271068/full.md

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Source: https://tomesphere.com/paper/PMC12271068