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. 2025 Oct;39(10):2563-2567.
doi: 10.1038/s41375-025-02757-6. Epub 2025 Sep 10.

Plasmapheresis facilitates soluble BCMA clearance and contributes to reversing primary resistance to anti-BCMA immunotherapy in multiple myeloma

Affiliations

Plasmapheresis facilitates soluble BCMA clearance and contributes to reversing primary resistance to anti-BCMA immunotherapy in multiple myeloma

Sven Neubert et al. Leukemia. 2025 Oct.
No abstract available

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Conflict of interest statement

Competing interests: The authors declare the following competing interests: JMW reports personal fees from Janssen, Sanofi, Takeda, Pfizer, Oncopeptides, Menarini-Stemline, Skyline Dx and GSK, and research support from BMS. KMK reports personal fees from Celgene, BMS, AbbVie, GSK, and Takeda; grants and personal fees from Janssen. HE reports grants and other support from Janssen, BMS, Amgen, GSK, and Sanofi, as well as further support from Takeda and Novartis. LR reports personal fees from BMS, Janssen, Pfizer, Amgen, GSK and Sanofi. All other authors declare no competing interests.

Figures

Fig. 1
Fig. 1. Multimodal debulking results in sBCMA clearance and subsequent response to BCMA× CD3 bispecific antibodies.
A Design of study including sBCMA-levels (ng/mL) in peripheral blood (PB), bone marrow (BM) and ultrafiltrate (UF) before and after plasmapheresis. B IgA levels in PB (mg/dL) and sBCMA levels (ng/mL) in BM and PB over the course of treatment, graphical view (upper panel), tabular view (lower panel). Abbreviations: Tec, teclistamab, PP plasmapheresis, D-P(A)CE daratumumab, cisplatin, cyclophosphamide, etoposide. Figure 1A created in BioRender under license https://BioRender.com/9gtlmss.
Fig. 2
Fig. 2. sBCMA limits in vitro efficacy of anti-BCMA immunotherapies.
A IL-2 (pg/mL) and B IFN-γ (pg/mL) levels were quantified by ELISA from co-culture supernatants after 20 h of incubation using ELISA MAX Deluxe Set for human IL-2 (431816, BioLegend) and human IFN-γ (430116, BioLegend). C Cytotoxic activity of belamaf was assessed in the presence of sBCMA using a luminescence-based viability assay with PBS as solvent control (**P < 0.005, ***P < 0.001, ****P < 0.0001). Abbreviations: IL-2 interleukin-2, IFN-γ interferon-gamma, cilta-cel ciltacabtagene autoleucel, BCMA B-cell maturation antigen, CAR chimeric antigen receptor, belamaf belantamab-mafodotin, solv. Ctr solvent control.

References

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