Daratumumab plus lenalidomide and dexamethasone for relapsed POEMS syndrome with bone plasmacytoma harboring 17p deletion

Int J Hematol. 2023 Mar;117(3):463-467. doi: 10.1007/s12185-022-03459-w. Epub 2022 Oct 6.

Abstract

The standard therapies for polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes (POEMS) syndrome are radiation therapy, high-dose chemotherapy followed by autologous stem cell transplantation, and lenalidomide combined with dexamethasone. Daratumumab was reported to be effective for treatment-naive and relapsed POEMS syndrome, but treatment options for relapsed POEMS syndrome with poor prognostic factors or cytogenetic abnormalities have not been established due to a lack of studies in these patients. Here, we describe a case of relapsed POEMS syndrome with bone plasmacytoma harboring a newly detected 17p deletion after high-dose chemotherapy followed by autologous stem cell transplantation and radiation therapy in a male patient. He was successfully treated with daratumumab plus lenalidomide and dexamethasone (Dara-Rd). Dara-Rd could be effective in relapsed POEMS syndrome with 17p deletion, which is known as a poor cytogenetic abnormality in multiple myeloma. This report may broaden the application of Dara-Rd for POEMS syndrome.

Keywords: Autologous stem cell transplantation; Cytogenetic abnormality; Monoclonal antibody; Plasma cell neoplasm; Radiation therapy.

Publication types

  • Case Reports

MeSH terms

  • Dexamethasone
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Lenalidomide / therapeutic use
  • Male
  • POEMS Syndrome* / drug therapy
  • Plasmacytoma* / drug therapy
  • Plasmacytoma* / genetics
  • Thalidomide
  • Transplantation, Autologous

Substances

  • Lenalidomide
  • daratumumab
  • Thalidomide
  • Dexamethasone