A nationwide prospective registry of bortezomib-based therapy in light chain (AL) amyloidosis

Leuk Lymphoma. 2022 Jan;63(1):205-211. doi: 10.1080/10428194.2021.1971215. Epub 2021 Aug 27.

Abstract

Until recently, no drug was labeled for AL amyloidosis. In 2011, the Italian Medicines Agency started a program to grant access to upfront bortezomib to patients with AL amyloidosis. All subjects were enrolled in a prospective online registry. Response was evaluated after two cycles to assess the possibility of continuing treatment. A total of 764 patients were included until 2019, and 615 were evaluable. Sixteen percent of patents had advanced (stage-IIIb) heart involvement, and 27% had severe or end-stage renal failure. Bortezomib delivery was possible in stage-IIIb patients at a reduced dose. Bortezomib discontinuation was associated with increasing age, advanced heart involvement and bi-weekly administration. Fifty-nine percent of subjects attained a hematologic response and 14% a cardiac response. Bortezomib-based therapy tends to be discontinued early in elderly patients and in advanced disease. Nevertheless, early response to therapy is possible in this challenging population.

Keywords: Amyloidosis; bortezomib; prospective registry; response.

MeSH terms

  • Aged
  • Amyloidosis* / diagnosis
  • Amyloidosis* / drug therapy
  • Bortezomib
  • Dexamethasone
  • Drug Therapy, Combination
  • Humans
  • Immunoglobulin Light-chain Amyloidosis* / diagnosis
  • Immunoglobulin Light-chain Amyloidosis* / drug therapy
  • Registries
  • Treatment Outcome

Substances

  • Bortezomib
  • Dexamethasone