ArticleEJHaem2026
BCMA CAR T for AL Amyloidosis After Plasmacytic Relapse of Lymphoplasmacytic Lymphoma.
Article in EJHaem, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06097832 (Phase 1b/2 Study of NXC-201 for the Treatment of Patients With Relapsed or Refractory AL Amyloidosis), which is not on this map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Phase 1b/2 Study of NXC-201 for the Treatment of Patients With Relapsed or Refractory AL Amyloidosis
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Lambda immunoglobulin light chain (AL) amyloidosis associated with non-IgM lymphoplasmacytic lymphoma (LPL) is rare and often refractory to conventional therapies. Treatment options for relapsed disease remain limited. Methods: Here we describe the case of a patient with a history of LPL-associated AL amyloidosis who had previously been treated with multiple B-cell- and plasma-cell-directed regimens. At the time of relapse, pathology demonstrated plasmacytic histology, with BCMA-expressing plasma cells by immunohistochemistry and no detectable B-cell infiltrate. The patient subsequently received investigational B-cell maturation antigen (BCMA)-directed chimeric antigen receptor (CAR) T-cell therapy. Results: Following BCMA-directed CAR T-cell therapy, the patient achieved a complete hematologic response. Conclusion: This case highlights the biologic complexity of LPL-associated AL amyloidosis and supports the use of BCMA-targeted therapy, especially when the relapsing or residual disease is comprised by the plasma cell component. Trial Registration: ClinicalTrials.gov identifier: NCT06097832.
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