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Annals of Hematology

, Volume 98, Issue 8, pp 1953–1959 | Cite as

Incidence of lymphoma in HIV-HCV-infected patients. Modifications in function of the anti-hepatitis C virus therapy

  • Daniel Gutiérrez-Saborido
  • Alicia Gutiérrez-Valencia
  • Carmen María González Domenech
  • Miguel Ángel López Ruz
  • Miguel Raffo Márquez
  • Mohamed Omar
  • José Antonio Girón-GonzálezEmail author
  • Grupo de Estudio de Hepatitis Virales (HEPAVIR) of the Sociedad Andaluza de Enfermedades Infecciosas (SAEI)
Original Article

Abstract

The change in the incidence of lymphomas in function of the presence or absence of sustained virological response after anti-hepatitis C therapy in a cohort of human immunodeficiency (HIV)-hepatitis C (HCV) viruses coinfected patients was analyzed. A prospective cohort of 755 HIV-HCV coinfected patients who received their first anti-HCV therapy, based on interferon + ribavirin schemas, was evaluated. Incidence and histologic types of lymphomas were analyzed in two periods: (1) before administration of anti-HCV therapy and (2) after anti-HCV therapy. The association between lymphoma incidence and demographic, HIV- (minimum CD4+ cell count and CD4+ cell count at diagnosis of lymphoma, antiretroviral therapy, maximal HIV load and HIV load at diagnosis of lymphoma) and HCV-related variables (HCV load, genotype, sustained viral response to anti-HCV therapy) were analyzed. A total of 13 lymphomas [incidence rate (95% confidence interval), 0.72 (0.33–1.11) × 1000 person-years, time from HIV diagnosis to lymphoma diagnosis (median, interquartile range), 15 (11–19) years] were diagnosed. Nine of them were non-Hodgkin and four Hodgkin lymphomas. The median CD4+ T cell count at diagnosis of lymphoma was 457/mm3, with only two cases with values lower than 200/mm3. The incidence rate of non-Hodgkin lymphomas was similar pre- and post-anti HCV therapy [0.33 (0.00–0.65) vs 0.68 (0.08–1.26) × 1000 person-years, respectively, p > 0.05]. Patients with sustained virologic HCV response showed similar incidence rate of lymphomas than that of those without anti-HCV response. In conclusion, anti-HCV therapy does not modify the incidence rate of lymphomas in HIV-HCV coinfected patients.

Keywords

HIV Hepatitis C virus Non-Hodgkin lymphoma Hodgkin lymphoma Interferon alpha Ribavirin 

Notes

Acknowledgments

The corresponding author had full access to all study data and final responsibility for the decision to submit for publication.

Authors’ contributions

Study conception and design: Gutiérrez-Saborido D, Girón-González JA.

Acquisition of data: Daniel Gutiérrez-Saborido, Alicia Gutiérrez-Valencia, Carmen María González Domenech, Miguel Angel López Ruz, Miguel Raffo Marquez, Mohamed Omar, José Antonio Girón-González.

Drafting of manuscript: Gutiérrez-Saborido D, Girón-González JA.

Critical revision: Daniel Gutiérrez-Saborido, Alicia Gutiérrez-Valencia, Carmen María González Domenech, Miguel Angel López Ruz, Miguel Raffo Marquez, Mohamed Omar, José Antonio Girón-González.

Compliance with ethical standards

The ethics committee of the Hospital Universitario Puerta del Mar, Cadiz (Spain) approved the study. Informed consent was obtained from all patients for being included in the study.

Conflict of interest

The authors declare that they have no competing interests.

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2019

Authors and Affiliations

  • Daniel Gutiérrez-Saborido
    • 1
  • Alicia Gutiérrez-Valencia
    • 2
  • Carmen María González Domenech
    • 3
  • Miguel Ángel López Ruz
    • 4
  • Miguel Raffo Márquez
    • 5
  • Mohamed Omar
    • 6
  • José Antonio Girón-González
    • 1
    Email author
  • Grupo de Estudio de Hepatitis Virales (HEPAVIR) of the Sociedad Andaluza de Enfermedades Infecciosas (SAEI)
  1. 1.Unidad de Enfermedades Infecciosas. Hospital Universitario Puerta del Mar. Facultad de Medicina, Instituto para la Investigación e Innovación en Ciencias Biomédicas de Cádiz (INiBICA)Universidad de CádizCádizSpain
  2. 2.Enfermedades Infecciosas, Microbiología y Medicina Preventiva. Instituto de Biomedicina de Sevilla/Hospital Universitario Virgen del Rocío/CSICUniversidad de SevillaSevillaSpain
  3. 3.Hospital Universitario Virgen de la Victoria, Málaga. Departamento de Microbiología, Facultad de FarmaciaUniversidad de GranadaGranadaSpain
  4. 4.Unidad Enfermedades Infecciosas, Facultad de Medicina. IBSHospital Universitario Virgen NievesGranadaSpain
  5. 5.Unidad Enfermedades InfecciosasHospital Juan Ramón JiménezHuelvaSpain
  6. 6.Unidad de Enfermedades InfecciosasComplejo Hospitalario de JaénJaénSpain

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