# Impact of modified dexamethasone administration sequence on infusion reaction incidence in HER2-positive breast cancer: a randomized multicenter trial

**Authors:** Ryoichi Matsunuma, Shigeru Nakagaki, Eiji Nakatani, Masayuki Kikuchi, Noriaki Wada, Kei Yonezawa, Tadahiro Isono, Ryosuke Hayami, Mayumi Kaga, Michiko Tsuneizumi

PMC · DOI: 10.1007/s12282-025-01752-0 · 2025-08-02

## TL;DR

Giving dexamethasone before HER2-targeted therapy in breast cancer patients significantly reduces infusion reactions without causing more side effects.

## Contribution

Demonstrates that premedication with dexamethasone before HER2 agents reduces infusion reactions in a randomized trial.

## Key findings

- Premedication with dexamethasone reduced first-cycle infusion reactions from 60% to 24%.
- No severe infusion reactions occurred in either group.
- Adverse event rates were similar between groups.

## Abstract

Infusion reactions (IRs) are common adverse events associated with HER2-targeted monoclonal antibodies, such as trastuzumab and pertuzumab. Although dexamethasone is routinely administered before docetaxel to prevent hypersensitivity, its optimal timing relative to HER2-targeted agents has not been established. This study assessed whether premedication with dexamethasone reduces the incidence of IRs associated with HER2-targeted therapy.

In this randomized, multicenter trial, 100 patients with HER2-positive early breast cancer were randomized to receive dexamethasone either before (experimental group) or after (control group) HER2-targeted agents. All patients received trastuzumab, pertuzumab, and docetaxel. The primary endpoint was the incidence of IRs during the first treatment cycle. Secondary endpoints included the incidence of grade ≥ 3 IRs, IRs in cycle 2, and overall adverse events.

Incidence of IRs in cycle 1 was significantly lower in the experimental group (24.0%) than in the control group (60.0%) (P < 0.001), corresponding to an absolute risk reduction of 36.0%. No grade ≥ 3 IRs occurred in either group. The incidence of IRs during cycle 2 was low and similar between groups (8.0% vs. 10.2%; P = 0.703). The incidence of treatment-related adverse events was similar between groups (98.0% vs. 100.0%, P > 0.999). Time-course analysis revealed that most of IRs in the control group occurred before dexamethasone administration.

Premedication with dexamethasone before HER2-targeted therapy substantially reduced IRs without additional toxicity. This straightforward, cost-effective modification to the premedication protocol may improve tolerability in HER2-positive breast cancer and other antibody-based therapies.

UMIN000045181 (registered on August 18, 2021).

## Linked entities

- **Proteins:** ERBB2 (erb-b2 receptor tyrosine kinase 2)
- **Chemicals:** dexamethasone (PubChem CID 5743), docetaxel (PubChem CID 148124)
- **Diseases:** HER2-positive breast cancer (MONDO:0006244)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** IRs (MESH:D000075662), toxicity (MESH:D064420), breast cancer (MESH:D001943), hypersensitivity (MESH:D004342)
- **Chemicals:** trastuzumab (MESH:D000068878), dexamethasone (MESH:D003907), pertuzumab (MESH:C485206), docetaxel (MESH:D000077143)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12552334/full.md

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Source: https://tomesphere.com/paper/PMC12552334