# Recurrent cytokine release syndrome in patients receiving bispecific antibody therapy for multiple myeloma: a case series

**Authors:** Roberta Della Pepa, Aldo Leone, Francesco Grimaldi, Simona Avilia, Mara Memoli, Bernardo Rossini, Carmine Liberatore, Fabrizio Pane

PMC · DOI: 10.1007/s00277-026-06966-6 · 2026-03-26

## TL;DR

This case series describes patients with multiple myeloma who experienced recurring cytokine release syndrome during bispecific antibody therapy, highlighting the need for better recognition and management of this side effect.

## Contribution

The paper reports a novel pattern of recurrent cytokine release syndrome beyond the initial treatment phase in bispecific antibody therapy for multiple myeloma.

## Key findings

- Five patients developed cyclic cytokine release syndrome episodes after initial treatment cycles.
- CRS episodes were typically mild and resolved with tocilizumab or corticosteroids.
- Recurrent CRS led to treatment discontinuation in one patient due to renal complications.

## Abstract

Bispecific antibodies targeting B-cell maturation antigen, BCMA (teclistamab) or G protein–coupled receptor, class C, group 5 member D, GPRC5D (talquetamab) are effective treatments for relapsed or refractory multiple myeloma. Their main early toxicity is cytokine release syndrome (CRS), usually transient and limited to initial cycles. We report five patients with relapsed or refractory multiple myeloma who received bispecific antibodies (n = 1 teclistamab; n = 4 talquetamab) who developed a pattern of recurrent, cyclic CRS beyond the initial step-up phase. All patients achieved at least a partial hematologic response, with complete or stringent complete remission in most cases. Recurrent febrile episodes occurred at regular intervals after drug administration, despite repeatedly negative infectious workups. CRS episodes were generally grade 1–2 and resolved with tocilizumab, with or without corticosteroids. In one patient treated with teclistamab, recurrent CRS contributed to treatment discontinuation due to renal complications. Attenuation of CRS severity over time was observed in some patients, allowing treatment continuation with tailored premedication strategies. This case series describes an unusual pattern of recurrent CRS occurring during bispecific antibody therapy for multiple myeloma. Recognition of this phenomenon is essential to avoid misdiagnosis as infection and unnecessary antimicrobial use. Systematic reporting of such real-world adverse events may help refine supportive care strategies.

## Linked entities

- **Genes:** TNFRSF17 (TNF receptor superfamily member 17) [NCBI Gene 608], GPRC5D (G protein-coupled receptor class C group 5 member D) [NCBI Gene 55507]
- **Diseases:** multiple myeloma (MONDO:0009693), cytokine release syndrome (MONDO:0600008)

## 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}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CD38 (CD38 molecule) [NCBI Gene 952] {aka ADPRC 1, ADPRC1, cADPR1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** infection (MESH:D007239), dysgeusia (MESH:D004408), leukocytosis (MESH:D007964), xerostomia (MESH:D014987), AL (MESH:D009101), Durie-Salmon IIIB (MESH:C566890), bacterial, viral, or fungal infections (MESH:D014777), weight loss (MESH:D015431), tumor (MESH:D009369), renal complications (MESH:D007674), oculomotor nerve palsy (MESH:D015840), onychodystrophy (OMIM:614149), immune dysregulation (OMIM:614878), fever (MESH:D005334), diarrhea (MESH:D003967), toxicities (MESH:D064420), Infectious (MESH:D003141), thrombocytosis (MESH:D013922), inflammatory (MESH:D007249), desquamative dermatitis (MESH:D017490), CRS (MESH:D000080424), Salmonella enteritidis infection (MESH:D012480), febrile (MESH:D000071072), RDP (MESH:C538001), CMV (MESH:D003586), bronchitis (MESH:D001991), COVID-19 (MESH:D000086382), hypogammaglobulinemia (MESH:D000361), interstitial nephritis (MESH:D009395), ageusia (MESH:D000370)
- **Chemicals:** Thalidomide (MESH:D013792), Dehamethasone (-), tocilizumab (MESH:C502936), lenalidomide (MESH:D000077269), paracetamol (MESH:D000082), tacrolimus (MESH:D016559), Bortezomib (MESH:D000069286), cetirizine (MESH:D017332), carfilzomib (MESH:C524865), ceftriaxone (MESH:D002443), daratumumab (MESH:C556306), Steroids (MESH:D013256), galactomannan (MESH:C012990), pomalidomide (MESH:C467566), dexamethasone (MESH:D003907), prednisone (MESH:D011241)
- **Species:** Human betaherpesvirus 6 (species) [taxon 10368], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Human alphaherpesvirus 1 (Herpes simplex virus type 1, no rank) [taxon 10298], Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC13018040