Emerging Risk of Campylobacter spp. Infection Associated With Anti-BCMA and Anti-GPRC5D Bispecific Antibodies - Scorecard - MDSpire

Emerging Risk of Campylobacter spp. Infection Associated With Anti-BCMA and Anti-GPRC5D Bispecific Antibodies

  • By

  • Idoia Bilbao

  • María Ansón

  • Sara Villar

  • Iñigo Pineda

  • Laura Gárriz

  • Manuel Pina-Sánchez

  • Luis-Esteban Tamariz-Amador

  • Paula Rodríguez-Otero

  • José Ramón Yuste

  • José L del Pozo

  • November 4, 2025

  • 0 min

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Clinical Scorecard: Increased Incidence of Campylobacter spp. Infections Linked to Bispecific Antibodies Targeting BCMA and GPRC5D

At a Glance

CategoryDetail
ConditionCampylobacter spp. infections in patients with relapsed/refractory multiple myeloma
Key MechanismsBispecific antibodies targeting BCMA and GPRC5D cause depletion of normal plasma cells leading to secondary hypogammaglobulinemia and increased infection risk
Target PopulationPatients with relapsed/refractory multiple myeloma treated with bispecific antibodies against BCMA and GPRC5D
Care SettingHematology and oncology clinical settings managing multiple myeloma

Key Highlights

  • Bispecific antibodies targeting BCMA and GPRC5D show efficacy but increase risk of infections due to hypogammaglobulinemia.
  • In a cohort of 85 patients, 9 developed Campylobacter infections including bloodstream and gastrointestinal episodes.
  • Secondary hypogammaglobulinemia and immunosuppression from therapy and disease contribute to vulnerability to Campylobacter spp.

Guideline-Based Recommendations

Diagnosis

  • Monitor for Campylobacter spp. infections in patients receiving BCMA and GPRC5D bispecific antibodies.
  • Use blood cultures and stool cultures or multiplex gastrointestinal panels for detection.
  • Perform species identification and antimicrobial susceptibility testing following EUCAST guidelines.

Management

  • Manage infections promptly with appropriate antimicrobial therapy guided by susceptibility testing.
  • Consider intravenous immunoglobulin therapy (IVIG) to address hypogammaglobulinemia.

Monitoring & Follow-up

  • Regularly measure serum immunoglobulin levels (IgG, IgA, IgM) monthly during treatment.
  • Monitor white blood cell counts, neutrophil and lymphocyte differentials, and serum albumin.
  • Surveillance for infectious complications should be intensified in the first 6 months of therapy.

Risks

  • Secondary hypogammaglobulinemia due to plasma cell depletion increases infection susceptibility.
  • Advanced age, frailty, comorbidities, and baseline immunosuppression further elevate infection risk.
  • Campylobacter infections can present as bloodstream or gastrointestinal disease in this population.

Patient & Prescribing Data

85 patients with relapsed/refractory multiple myeloma treated with bispecific antibodies targeting BCMA and GPRC5D

Treatment with these bispecific antibodies is associated with a notable incidence of Campylobacter infections, necessitating targeted infection prevention and monitoring strategies.

Clinical Best Practices

  • Implement targeted surveillance for Campylobacter spp. infections in patients receiving BCMA and GPRC5D bispecific antibodies.
  • Regularly assess immunoglobulin levels and consider IVIG supplementation to mitigate hypogammaglobulinemia.
  • Promptly investigate and treat suspected infections with culture and susceptibility-guided antimicrobials.
  • Recognize patient-related risk factors such as age and comorbidities to tailor preventive strategies.

References

Original Source(s)

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