# Frequency-adjusted daratumumab-based regimen versus bortezomib/dexamethasone in newly diagnosed AL amyloidosis: a matched-cohort study

**Authors:** Wanting Zheng, Meilan Zhou, Yan Xing, Jin Zhao, Baojian Liu, Wenjing Li, Shiren Sun

PMC · DOI: 10.1080/07853890.2026.2617767 · Annals of Medicine · 2026-01-21

## TL;DR

A frequency-adjusted daratumumab regimen improves treatment responses in AL amyloidosis compared to bortezomib/dexamethasone.

## Contribution

A cyclophosphamide-free, frequency-adjusted daratumumab regimen is shown to improve response rates in AL amyloidosis.

## Key findings

- The Dara-based regimen achieved higher complete response rates at 6 and 12 months compared to BD.
- Organ responses, including cardiac and renal, were significantly better with the Dara regimen.
- Safety profiles were comparable between the two treatment groups.

## Abstract

The optimal dosing schedule for daratumumab (Dara) in newly diagnosed systemic light-chain (AL) amyloidosis requires refinement. This real-world study compared the efficacy and safety of a frequency-adjusted, cyclophosphamide-free Dara-based regimen with bortezomib/dexamethasone (BD).

We included newly diagnosed AL amyloidosis patients treated between January 2018 and December 2024, with follow-up data censored in August 2025. Using 1:1 propensity score matching based on age, cardiac stage, dFLC, and organ function, we compared hematologic/organ responses and survival. Survival was analyzed with Kaplan-Meier and log-rank tests. The Dara-based group received a cyclophosphamide-free regimen with an adjusted schedule (biweekly in cycle 1, then monthly) and a response-guided treatment duration.

A total of 105 patients were included. After propensity score matching, 60 patients (30 per group) were selected for comparative analysis. The Dara-based group achieved significantly higher hematologic complete response (CR) rates at 6 months (57% vs. 27%, p = 0.018) and 12 months (63% vs. 27%, p = 0.002), with a markedly shorter median time to CR (61 vs. 120 days, p = 0.010). Organ responses were also superior: cardiac response 52% vs. 24% (p = 0.037) and renal response 56% vs. 27% (p = 0.037). No significant survival difference was observed during follow-up, and the safety profile was comparable between groups.

A frequency-adjusted Dara-based regimen induces significantly faster and deeper hematologic and organ responses compared to BD in newly diagnosed AL amyloidosis which offers a promising personalized approach to reduce treatment burden and adverse events while maintaining high efficacy, supporting its integration into clinical practice for a broader patient population.

## Linked entities

- **Chemicals:** bortezomib (PubChem CID 387447), dexamethasone (PubChem CID 5743), cyclophosphamide (PubChem CID 2907)
- **Diseases:** AL amyloidosis (MONDO:0019438)

## Full-text entities

- **Genes:** CD38 (CD38 molecule) [NCBI Gene 952] {aka ADPRC 1, ADPRC1, cADPR1}, TNNI3 (troponin I3, cardiac type) [NCBI Gene 7137] {aka CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI}
- **Diseases:** acute kidney injury (MESH:D058186), AL (MESH:D009101), multiorgan failure (MESH:D051437), plasma cell proliferative disorder (MESH:D007952), MOD (MESH:C564833), proteinuria (MESH:D011507), fatigue (MESH:D005221), tumor (MESH:D009369), organ dysfunction (MESH:D009102), toxicity (MESH:D064420), critically ill (MESH:D016638), peripheral neuropathy (MESH:D010523), BD (MESH:C563177), amyloid (MESH:C000718787), poorly controlled diabetes (MESH:D003920), organ damage (MESH:D000092124), heart failure (MESH:D006333), death (MESH:D003643), disease (MESH:D004194), edema (MESH:D004487), end-stage renal disease (MESH:D007676), AL amyloidosis (MESH:D000075363), cardiac (MESH:D006331), Amyloidosis (MESH:D000686), VGPR (MESH:D000326), diarrhea (MESH:D003967)
- **Chemicals:** cyclophosphamide (MESH:D003520), Dara (MESH:C556306), DARA (MESH:C000634424), D-VCd (-), dexamethasone (MESH:D003907), bortezomib (MESH:D000069286)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12825582/full.md

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Source: https://tomesphere.com/paper/PMC12825582