AI Article Synopsis

  • Anti-CD38 monoclonal antibodies improve outcomes for patients with plasma cell dyscrasia (PCD) but increase the risk of infections like cytomegalovirus (CMV) reactivation.
  • A retrospective study involving 154 PCD patients found that 38% of those tested for CMV reactivation showed positive results, with some experiencing mild symptoms and others developing serious conditions.
  • The reactivation of CMV significantly impacted treatment by causing dose adjustments and delays in anti-PCD therapies, highlighting the need for monitoring during anti-CD38 mAb treatment.

Article Abstract

Introduction: Anti-CD38 monoclonal antibodies (mAbs) have improved the prognosis of patients with plasma cell dyscrasia (PCD), but are also associated with increased infectious adverse events. Cytomegalovirus (CMV) is a common latent pathogen that is reactivated in immunocompromised individuals. Although CMV reactivation has mostly been reported after high-dose chemotherapy followed by stem cell transplantation in patients with PCD, cases of reactivation during anti-CD38 mAb therapy have been reported recently. Due to limited studies, we aimed to determine the frequency and impact of CMV reactivation during anti-CD38 mAb therapy.

Patients And Methods: This retrospective analysis included 154 consecutive patients with PCD who were treated with anti-CD38 mAbs at a single institution.

Results: Seventy-six patients were evaluated for CMV reactivation by CMV pp65 antigen testing, and 29 (38%) patients, including nine with newly diagnosed PCD, showed positive results. Patients who tested positive for the CMV pp65 antigen had substantially lower serum albumin levels than those who tested negative. However, the two groups showed no marked difference in the concurrent anti-PCD medications or baseline absolute lymphocyte count. Although most patients showing positive results in the CMV pp65 antigen test had mild or no symptoms, with fever being the most common symptom, some patients developed CMV end-organ disease. In addition, CMV reactivation interfered with the course of anti-PCD treatment in most patients, necessitating dose reductions, delays, and discontinuation of chemotherapy.

Conclusion: This study provides an overview of the clinical impact of CMV reactivation in patients with PCD treated with anti-CD38 mAb-containing regimens.

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Source
http://dx.doi.org/10.1016/j.clml.2024.03.012DOI Listing

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