# Flat dose intravenous immunoglobulin primary infection prophylaxis in multiple myeloma patients on BCMA and GPRC5D bispecific antibody therapy: the Vanderbilt experience

**Authors:** Naimisha Marneni, Spencer Lessans, Bhagirathbhai Dholaria, Salyka Sengsayadeth, Eden A. Biltibo, Vivek Patel, Shakthi Bhaskar, Reena Jayani, Sanjay Mohan, Ashwin Kishtagari, David Morgan, Olalekan O. Oluwole, Bipin N. Savani, Adetola A. Kassim, Muhamed Baljevic

PMC · DOI: 10.3389/fimmu.2026.1721820 · Frontiers in Immunology · 2026-02-19

## TL;DR

This study examines the use of flat-dose IVIG to prevent infections in multiple myeloma patients receiving bispecific antibody therapy.

## Contribution

The study introduces flat-dose IVIG as a feasible alternative to weight-based IVIG for infection prophylaxis in this patient group.

## Key findings

- 73% of patients experienced at least one infection, and 43% had two or more.
- 27% of infections were classified as grade three or higher in severity.
- Flat-dose IVIG was found to be feasible for primary infection prophylaxis.

## Abstract

Bispecific antibodies (BsAbs) can cause profound hypogammaglobulinemia. Conventional infection prophylaxis has utilized weight-based IVIG dosing. However, the use of flat IVIG dosing can significantly reduce IVIG utilization. We evaluated hypogammaglobulinemia and infection risk in relapsed/refractory multiple myeloma (RRMM) patients treated with BsAbs who received flat-dose IVIG for primary infection prophylaxis. Among thirty patients, 73% had ≥1 and 43% had ≥2 infectious episodes. By severity, 27% of infections were CTCAE v5 grade three or higher and there were 2 sepsis-related deaths. Overall, flat-dose IVIG demonstrates feasibility for primary infection prophylaxis in RRMM patients receiving BsAbs.

## Linked entities

- **Proteins:** TNFRSF17 (TNF receptor superfamily member 17), GPRC5D (G protein-coupled receptor class C group 5 member D)
- **Diseases:** multiple myeloma (MONDO:0009693)

## Full-text entities

- **Genes:** GPRC5D (G protein-coupled receptor class C group 5 member D) [NCBI Gene 55507], TNFRSF17 (TNF receptor superfamily member 17) [NCBI Gene 608] {aka BCM, BCMA, CD269, TNFRSF13A}, CD38 (CD38 molecule) [NCBI Gene 952] {aka ADPRC 1, ADPRC1, cADPR1}
- **Diseases:** Neutropenia (MESH:D009503), deaths (MESH:D003643), viral infections (MESH:D014777), Infection (MESH:D007239), bone marrow plasmacytosis (MESH:D001855), cytokine release syndrome (MESH:D000080424), bacterial infections (MESH:D001424), ISS (MESH:C564479), sepsis (MESH:D018805), Infectious episodes (MESH:D003141), disease (MESH:D004194), respiratory tract infections (MESH:D012141), neurotoxicity (MESH:D020258), MM (MESH:D009101), lymphopenia (MESH:D008231), DM (MESH:D009223), BD (MESH:D001528), hypogammaglobulinemia (MESH:D000361), CRS (MESH:D003398)
- **Chemicals:** daratumumab (MESH:C556306), trimethoprim-sulfamethoxazole (MESH:D015662), penta (MESH:C064764), levofloxacin (MESH:D064704), valacyclovir (MESH:D000077483), BCMA (MESH:C048009)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12960612/full.md

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Source: https://tomesphere.com/paper/PMC12960612