Epidemiology and Risk Factors for the Development of Infectious Complications in Newly Diagnosed Multiple Myeloma: A Multicenter Prospective Cohort Study in Latin America

Author:

Bove Virginia1ORCID,Riva Eloísa2ORCID,Vásquez Jule3ORCID,Peña Camila4ORCID,Seehaus Cristian5,Samanez César6ORCID,Bustos Justina7,Hernández Marcos8,Fernández Julio9,Ríos Oliday10,Rodríguez Yusaima10,Figueredo Irving11ORCID,Fantl Dorotea5ORCID,Malpica Luis12ORCID

Affiliation:

1. Department of Hematology, Hospital Central de las FF.AA., Montevideo, Uruguay

2. Department of Hematology, Hospital de Clínicas, Montevideo, Uruguay

3. Department of Medical Oncology, Instituto Nacional de Enfermedades Neoplasicas, Lima, Peru

4. Department of Hematology, Hospital del Salvador, Santiago, Chile

5. Department of Hematology, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina

6. Department of Medical Oncology, Oncosalud—AUNA, Lima, Peru

7. Department of Hematology and Bone Marrow Transplantation, Instituto Oncológico Nacional, Panamá, Panamá

8. Department of Hematology, Universidad de Carabobo, Hospital Metropolitano del Norte, Carabobo, Venezuela

9. Department of Hematology, Hospital General Universitario Dr Gustavo Aldereguía Lima, Cienfuegos, Cuba

10. Department of Hematology, Hospital Hermanos Ameijeiras, La Habana, Cuba

11. Department of Hematology, Centro de Investigaciones Médico Quirúrgicas, La Habana, Cuba

12. Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX

Abstract

PURPOSE Infections are a significant cause of morbidity and mortality in patients with multiple myeloma (MM). In Latin America, data on infectious complications in this patient population are lacking. METHODS We conducted a prospective cohort study of patients with newly diagnosed MM (NDMM) in seven Latin American countries between June 2019 and May 2020. Patients with active disease, on active therapy, and with a follow-up of 6 months from the time of diagnosis were included. Our primary end point was the number of infectious events that required hospitalization for ≥ 24 hours. RESULTS Of 248 patients with NDMM, 89 (35.9%) had infectious complications (113 infectious events), the majority (67.3%) within the first 3 months from diagnosis. The most common sites of infection were respiratory (38%) and urinary tract (31%). The microbial agent was identified in 57.5% of patients with gram-negative bacteria (73.5%) as the most common pathogen. Viral infections were infrequent, and no patients with fungal infection were reported. In the multivariable analysis, diabetes mellitus (odds ratio [OR], 2.71; 95% CI, 1.23 to 6.00; P = .014), creatinine ≥ 2 mg/dL (OR, 4.87; 95% CI, 2.29 to 10.35; P < .001), no use of trimethoprim-sulfamethoxazole prophylaxis (OR, 6.66; 95% CI, 3.43 to 12.92; P < .001), and treatment with immunomodulatory drugs (OR, 3.02; 95% CI, 1.24 to 6.29; P = .003) were independent factors associated with bacterial infections. At 6 months, 21 patients (8.5%) had died, 47.6% related to infectious complications. CONCLUSION Bacterial infections are a substantial cause of hospital admissions and early death in patients with NDMM. Antibiotic prophylaxis should be considered to reduce infectious complications in patients with MM.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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