# Doxycycline Plus Bortezomib-Containing Regimens for the Treatment of Light-Chain Amyloidosis in the Frontline Setting: Experience from the Amyloidosis Program of Calgary

**Authors:** Ellen Lewis, Nowell Fine, Sylvia McCulloch, Jason Tay, Peter Duggan, Paola Neri, Nizar Bahlis, Victor H. Jimenez-Zepeda

PMC · DOI: 10.3390/curroncol31090415 · Current Oncology · 2024-09-18

## TL;DR

Adding doxycycline to bortezomib-based treatment for AL amyloidosis did not improve survival or cardiac outcomes in a retrospective study.

## Contribution

This study evaluates the clinical impact of adding doxycycline to bortezomib-containing regimens in newly diagnosed AL amyloidosis patients.

## Key findings

- No significant differences in overall response rate or progression-free survival between BCR and BCR-D groups.
- Doxycycline addition did not improve organ responses or cardiac outcomes in AL amyloidosis patients.
- Retrospective analysis showed no benefit of doxycycline in prolonging overall survival.

## Abstract

Background: Pre-clinical and retrospective data suggest that doxycycline added to treatment regimens has benefit in AL amyloidosis. However, a recent multicenter, open-label, randomized controlled trial in AL amyloidosis patients treated with CyBorD did not demonstrate a progression-free survival (PFS) or cardiac PFS benefit with added doxycycline. Objective: The main objective of this study was to explore the role of doxycycline combined with bortezomib-containing regimens (BCRs) for newly diagnosed AL amyloidosis patients with cardiac involvement and to compare them with a cohort of concurrent patients treated with BCR only. Material and Methods: AL amyloidosis patients, newly diagnosed between January 2012 and March 2022, who were treated with BCR at the Amyloidosis Program of Calgary (APC) were evaluated. Results: Sixty-four concurrent patients were identified. Thirty-nine patients received doxycycline in addition to BCR (BCR-D) for a median of 8 months. The overall response rate was similar among the groups. No significant differences in VGPR/CR, dFLC at 1 month, time to first response, time to best response, or organ responses were noted between the BCR alone and BCR-D groups. Summary and Conclusions: Our retrospective study demonstrated that doxycycline combined with BCR failed to prolong OS, PFS, or cardiac responses compared with BCR alone in patients with cardiac AL amyloidosis.

## Linked entities

- **Chemicals:** doxycycline (PubChem CID 54671203), bortezomib (PubChem CID 387447)
- **Diseases:** AL amyloidosis (MONDO:0019438)

## Full-text entities

- **Genes:** BCR (BCR activator of RhoGEF and GTPase) [NCBI Gene 613] {aka ALL, BCR1, CML, D22S11, D22S662, PHL}
- **Diseases:** cardiac involvement (MESH:D006331), AL amyloidosis (MESH:D000075363), Amyloidosis (MESH:D000686)
- **Chemicals:** Doxycycline (MESH:D004318), Bortezomib (MESH:D000069286), CyBorD (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11431705/full.md

## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC11431705/full.md

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Source: https://tomesphere.com/paper/PMC11431705