# Addition of daratumumab to standard triplet regimens achieved better survival in newly diagnosed multiple myeloma: a systematic review and meta-analysis of randomized controlled trials

**Authors:** Bin Hu, Jun Wang, Dan Fang, Ling Jiang, Tianqi Li, Jinxia Cao

PMC · DOI: 10.3389/fonc.2025.1619115 · Frontiers in Oncology · 2025-10-30

## TL;DR

Adding daratumumab to standard treatments for newly diagnosed multiple myeloma improves survival and response rates, though some side effects increase.

## Contribution

A meta-analysis showing that adding daratumumab to triplet regimens improves outcomes in newly diagnosed multiple myeloma patients.

## Key findings

- Daratumumab addition improved overall survival and complete response rates in multiple myeloma patients.
- Quadruplet regimens achieved higher minimal residual disease negativity and prolonged progression-free survival.
- Safety profile showed increased risks of lymphopenia and infections but remained acceptable.

## Abstract

Triplet regimens, such as bortezomib-lenalidomide-dexamethasone (VRd) and bortezomib-melphalan-prednisone (VMP), were standard treatments for newly diagnosed multiple myeloma (NDMM), but they were non-curative for most patients. The incorporation of daratumumab into these regimens, resulting in quadruplet therapies, has shown improved outcomes, though concerns over increased toxicity remain.

In this systematic review and meta-analysis, we aimed to compare the efficacy and safety of daratumumab-incorporated quadruplet regimens versus traditional triplet regimens in NDMM. A search of PubMed, EMBASE, and the Cochrane Library identified six randomized controlled trials (RCTs) with 3,056 patients. Outcomes included response rates, minimal residual disease (MRD) negativity rate, progression-free survival (PFS), and adverse events.

Compared with triplet regimens, daratumumab-incorporated quadruplet combinations achieved a higher overall survival rate (ORR) (pooled OR = 2.36, 95% CI: 1.56-3.56, P < 0.0001), rate of complete response (CR) or better (pooled OR = 2.35, 95% CI: 1.99-2.77, P < 0.0001), very good partial response (VGPR) or better (pooled OR = 2.58, 95% CI: 1.76-3.79, P < 0.0001) and MRD negativity (pooled OR = 3.55, 95% CI: 2.54-4.96, P < 0.0001). The addition of daratumumab to triplet regimens significantly improved PFS compared with triplet regimens (pooled HR = 0.45, 95% CI: 0.39–0.52, P < 0.0001). Regarding safety, quadruplet regimens were associated with a higher incidence of lymphopenia, upper respiratory tract infection, pyrexia, and pneumonia.

Incorporating daratumumab into backbone triplet regimens is associated with improved response rates, deeper remission and prolonged PFS with acceptable toxicity profile in patients with NDMM.

https://inplasy.com/inplasy-2024-12-0026/, identifier INPLASY2024120026.

## Linked entities

- **Chemicals:** bortezomib (PubChem CID 387447), lenalidomide (PubChem CID 216326), dexamethasone (PubChem CID 5743), melphalan (PubChem CID 460612), prednisone (PubChem CID 5865)
- **Diseases:** multiple myeloma (MONDO:0009693)

## Full-text entities

- **Diseases:** lymphopenia (MESH:D008231), upper respiratory tract infection (MESH:D012141), toxicity (MESH:D064420), pneumonia (MESH:D011014), NDMM (MESH:D009101), pyrexia (MESH:D005334)
- **Chemicals:** daratumumab (MESH:C556306), melphalan (MESH:D008558), prednisone (MESH:D011241), lenalidomide (MESH:D000077269), VMP (-), 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

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12611664/full.md

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Source: https://tomesphere.com/paper/PMC12611664