# Pharmacotherapy agents in prevention and treatment of breast cancer-related lymphedema: a systematic scoping review

**Authors:** Caroline Lommer, Lila Schroeder, Caroline Amato, Kerry Dhakal, Caitlin Kotian, Dionisia Quiroga, Electra D. Paskett, Mei R. Fu, Ann Scheck McAlearney, Stephanie Collins, Tari A. King, Sarah A. McLaughlin, Sara P. Myers

PMC · DOI: 10.3389/fonc.2026.1751628 · Frontiers in Oncology · 2026-03-04

## TL;DR

This review explores whether drugs or herbal treatments can prevent or treat lymphedema in breast cancer survivors, finding limited evidence that some agents may help.

## Contribution

The study is the first systematic scoping review to comprehensively evaluate pharmacologic and herbal agents for breast cancer-related lymphedema.

## Key findings

- GLP-1 receptor agonists may reduce the risk of breast cancer-related lymphedema.
- Immunomodulatory agents may improve signs and symptoms of lymphedema.
- Most tested drugs and supplements showed no benefit or inconsistent results in treating lymphedema.

## Abstract

Breast cancer-related lymphedema (BCRL) is a common and life-long adverse event affecting ~20% of breast cancer survivors. As existing non-pharmacologic management is burdensome, expensive, and variably effective, this systematic scoping review aims to identify pharmacologic and herbal agents for prevention and treatment for BCRL.

PubMED, Embase, Web of Science Core collection, and the Cumulative Index to Nursing and Allied Health Literature were searched for studies published in English between 1993 and 2025 that investigated the preventative or therapeutic effect of pharmacologic or herbal agents on BCRL among adult stage I-III breast cancer patients. Studies describing interventions with systemically absorbed anti-inflammatories, anti-thrombotics, anti-coagulants, and blood product components were included. Systematic reviews, protocols for ongoing clinical trials, preclinical and non-human studies, editorials, and studies not exclusive to BCRL were excluded. Three reviewers screened and extracted data between June and August 2025. The primary outcomes of interest were reduction in BCRL incidence or severity.

Of the 217 articles screened, 37 were included in the final review. After full text review, 13 were excluded for repetitive data, non-English language, or irrelevant outcomes. The 24 studies included in the analysis investigated anti-diabetic, herbal, anti-inflammatory, anti-hypertensive, immunomodulatory, and microbiome modifying agents, and venoactive flavinoid derivates. Three studies explored the role of pharmacologic/herbal agents in BCRL prevention. While thiazolidinediones, anti-hypertensives, and non-steroidal anti-inflammatory drugs (NSAIDs) had no effect on BCRL incidence, glucagon-like peptide-1 receptor agonists (GLP-1 RA) were associated with BCRL prevention. In the 21 studies that assessed the effect of pharmacologic/herbal agents in BCRL treatment, NSAIDs/steroids, anti-hypertensives, microbiome/synbiotic supplements, and doxycycline showed no benefit and data for flavonoid-derived venoactive agents and herbal products were inconsistent. Immune-modulating therapies were associated with improved BCRL signs/symptoms in three studies.

This systematic scoping review found limited evidence suggesting that GLP-1 RAs may reduce the risk of BCRL and that immunomodulatory agents may improve signs/symptoms of BCRL. Rigorous prospective trials using standardized limb volume/edema, quality-of-life (QoL), and symptom measures and longer follow-up are needed to inform clinical practice aimed at preventing and treating BCRL.

https://www.crd.york.ac.uk/PROSPERO/, identifier CRD420251055134.

## Linked entities

- **Chemicals:** doxycycline (PubChem CID 54671203)
- **Diseases:** breast cancer (MONDO:0004989), lymphedema (MONDO:0019297)

## Full-text entities

- **Genes:** GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}
- **Diseases:** diabetic (MESH:D003920), lymphedema (MESH:D008209), BCRL (MESH:D000072656), inflammatory (MESH:D007249), thrombotics (MESH:D013927), edema (MESH:D004487), Breast cancer-related (MESH:D001943), hypertensive (MESH:D006973)
- **Chemicals:** flavinoid derivates (-), steroids (MESH:D013256), flavonoid (MESH:D005419), doxycycline (MESH:D004318), thiazolidinediones (MESH:D045162)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12995638/full.md

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Source: https://tomesphere.com/paper/PMC12995638