[Listeria meningitis during daratumumab/bortezomib/dexamethasone therapy in a patient with multiple myeloma]

Tomoki Fujii1,2, Nobuhiro Ohno1, Shinsuke Kitahara1,2

  • 1Department of Hematology, Kantoh Rosai Hospital.

Insights

A multiple myeloma patient developed Listeria meningitis after discontinuing antibiotic prophylaxis during daratumumab-based chemotherapy. This highlights the need for continued prophylaxis, such as sulfamethoxazole/trimethoprim, during CD38-targeted therapy.

Area of Science:

  • * Hematology
  • * Infectious Diseases
  • * Oncology

Background:

  • * Multiple myeloma is a hematologic malignancy treated with chemotherapy regimens.
  • * Daratumumab (DARA), a CD38-targeted therapy, is used in multiple myeloma treatment.
  • * Prophylaxis with sulfamethoxazole/trimethoprim (ST) is common during chemotherapy.

Observation:

  • * An 88-year-old woman with multiple myeloma received third-line daratumumab, bortezomib, and dexamethasone (DBd) chemotherapy.
  • The patient achieved remission, and dexamethasone dose was reduced, leading to discontinuation of ST prophylaxis.
  • After 28 cycles of DBd, the patient presented with fever and altered consciousness.

Findings:

  • * The patient was diagnosed with Listeria monocytogenes (LM) meningitis.
  • * CD38 inactivation, a mechanism of daratumumab, is linked to increased susceptibility to LM infections.
  • Discontinuation of ST prophylaxis coincided with the LM meningitis diagnosis.

Implications:

  • * Patients undergoing CD38-targeted therapy, like daratumumab, may be at increased risk for Listeria infections.
  • * Antibiotic prophylaxis, specifically with agents like ST that target Listeria, should be strongly considered during daratumumab-based chemotherapy.
  • Close monitoring for infections is crucial in immunocompromised patients receiving novel cancer therapies.