# The Effect of Bevacizumab Therapy on Reducing Erythrocyte Transfusion Requirements and Preventing Iron Deficiency in Patients With Hereditary Hemorrhagic Telangiectasia

**Authors:** Öznur Aydın, Fatoş Dilan Köseoğlu, Selim Sayın, Hilmi Erdem Gözden, Onur Şahin, Ünal Ataş, Derya Deniz Kürekci, Sude Hatun Aktimur, Meltem Aylı, Mehmet Turgut, Serkan Güven

PMC · DOI: 10.7759/cureus.102365 · Cureus · 2026-01-27

## TL;DR

This study shows that bevacizumab therapy reduces blood transfusions and improves iron levels in patients with hereditary hemorrhagic telangiectasia.

## Contribution

The study provides evidence that IV bevacizumab improves iron parameters and reduces transfusion needs in HHT patients.

## Key findings

- Bevacizumab therapy reduced erythrocyte transfusion requirements from 6 to 0 units.
- IV iron dose requirements decreased from 5000 mg to 2000 mg after bevacizumab treatment.
- Treated patients had higher hemoglobin and ferritin levels compared to untreated patients.

## Abstract

Objective: This multicenter retrospective cohort study aimed to evaluate the association between intravenous (IV) bevacizumab therapy and iron-related parameters and transfusion burden in patients with hereditary hemorrhagic telangiectasia (HHT) in Turkey.

Methods: Thirty-five genetically or clinically confirmed HHT patients from tertiary centers were included. Patients receiving IV bevacizumab (n=15) were compared with those without bevacizumab exposure (n=20). Longitudinal hematologic parameters, annual IV iron dose, erythrocyte suspension (ES) transfusion volume, and bleeding frequency were recorded. In the bevacizumab group, pre- and post-treatment values were compared.

Results: Before treatment, patients who subsequently received bevacizumab had higher ES transfusion requirements than untreated patients (median 6 vs. 2 units; p=0.029). After bevacizumab therapy, IV iron requirement decreased (median 5000 mg to 2000 mg; p=0.005) and ES transfusion burden declined (median 6 to 0 units; p=0.002). Compared with the non-bevacizumab group, treated patients had higher final hemoglobin (p=0.042) and ferritin levels (p=0.048), while transferrin saturation was higher in the untreated group (p=0.047).

Conclusion: In this multicenter retrospective cohort, IV bevacizumab therapy was associated with improved iron parameters and reduced transfusion requirements in patients with HHT-related bleeding.

## Linked entities

- **Diseases:** hereditary hemorrhagic telangiectasia (MONDO:0019180)

## Full-text entities

- **Genes:** TF (transferrin) [NCBI Gene 7018] {aka HEL-S-71p, PRO1557, PRO2086, TFQTL1}, ACVRL1 (activin A receptor like type 1) [NCBI Gene 94] {aka ACVRLK1, ALK-1, ALK1, HHT, HHT2, ORW2}, ENG (endoglin) [NCBI Gene 2022] {aka END, HHT1, ORW1}, GDF2 (growth differentiation factor 2) [NCBI Gene 2658] {aka BMP-9, BMP9, HHT5}, SMAD4 (SMAD family member 4) [NCBI Gene 4089] {aka DPC4, JIP, MADH4, MYHRS}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}
- **Diseases:** anemia (MESH:D000740), thrombosis (MESH:D013927), toxicity (MESH:D064420), AVMs (MESH:D001165), gastrointestinal bleeding (MESH:D006471), chronic bleeding (MESH:D002908), mucocutaneous telangiectasias (MESH:D013684), ES (MESH:D012010), Vascular Diseases (MESH:D014652), HHT (MESH:D013683), Bleed (MESH:D006470), AVM (MESH:D002538), Epistaxis (MESH:D004844), autosomal dominant vascular disorder (MESH:D030342), iron deficiency anemia (MESH:D018798), Iron Deficiency (MESH:D000090463), visceral (MESH:D007418)
- **Chemicals:** ES (-), tacrolimus (MESH:D016559), sirolimus (MESH:D020123), pomalidomide (MESH:C467566), tranexamic acid (MESH:D014148), Iron (MESH:D007501), Thalidomide (MESH:D013792), Bevacizumab (MESH:D000068258)
- **Species:** Homo sapiens (human, species) [taxon 9606], Meleagris gallopavo (common turkey, species) [taxon 9103]

## Full text

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12936807/full.md

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Source: https://tomesphere.com/paper/PMC12936807