<p>There is limited data on the efficacy of combined antiviral treatment for immunosuppressed COVID-19 patients. We describe the clinical and microbiological outcomes of a cohort of oncohaematological patients with persistent SARS-CoV-2 infection who received different dual and triple antiviral combination treatments. We selected the 15 patients (two of them with two episodes) who were prescribed combined anti-SARS-CoV-2 treatment in our institution (October 2021–December 2024). Combined antiviral therapy was administered as a compassionate use in the following indications: (i) persistence of SARS-CoV-2 positive quantitative RT-PCR (qRT-PCR) for &gt; 14&#xa0;days despite antiviral monotherapy and severe COVID-19 or (ii) need to achieve viral clearance before hematopoietic progenitor transplantation or administration of immuno-chemotherapy. Samples corresponding to positive qRT-PCR results with a Ct value &lt; 32 were analysed by whole-genome sequencing. In 13 out of a total of 15 episodes, with control qRT-PCR after the combination therapy, with positivity periods ranging from 12 to 235&#xa0;days, viral clearance was achieved 10–69&#xa0;days after receiving the combination therapy. Whole genome sequencing revealed the emergence of resistance mutations in three cases prior to combination therapy. The therapy was able to overcome these mutations and lead to clearance. Genomic analysis identified one patient with three consecutive reinfections that had been mismanaged as persistent infection. In conclusion, combined antiviral treatment leads to satisfactory clinical and microbiological outcomes in a small cohort of immunocompromised patients with persistent SARS-CoV-2 infection. Early monotherapy treatment in these patients was associated with a high rate of clinical and microbiological failure, with sporadic documentation of resistance mutations that were overcome with combined antiviral therapy.</p>

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Evaluation of the efficiency of combined antiviral therapy in COVID-19 challenging immunocompromised patients

  • Marta López-Llaría,
  • Francisco Tejerina,
  • María Ferris,
  • Isabel Regalado-Artamendi,
  • Guadalupe Bernal,
  • Pilar Catalán,
  • Cristina Veintimilla,
  • Lara Mesones,
  • Leire Perez Latorre,
  • Chiara Fanciulli,
  • Teresa Aldamiz,
  • Cristina Diez,
  • Roberto Alonso,
  • Patricia Muñoz,
  • Laura Pérez-Lago,
  • Darío García de Viedma,
  • Alcalá Luis,
  • Aldámiz Teresa,
  • Alonso Roberto,
  • Álvarez-Uría Ana,
  • Bermúdez Elena,
  • Bouza Emilio,
  • Buenestado-Serrano Sergio,
  • Burillo Almudena,
  • Catalán Pilar,
  • Cercenado Emilia,
  • Díez Cristina,
  • Escribano Pilar,
  • Estévez Agustín,
  • Fanciulli Chiara,
  • Galar Alicia,
  • García Mª Dolores,
  • García de Viedma Darío,
  • Guinea Jesús,
  • Herranz Marta,
  • Irigoyen Álvaro,
  • Kestler Martha,
  • López Juan Carlos,
  • Machado Marina,
  • Marín Mercedes,
  • Martín-Rabadán Pablo,
  • Molero-Salinas Andrea,
  • Montilla Pedro,
  • Muñoz Patricia,
  • Palomo María,
  • Pérez-Granda María Jesús,
  • Pérez-Lago Laura,
  • Pérez Leire,
  • Reigadas Elena,
  • Rincón Cristina,
  • Rodríguez Belén,
  • Rodríguez Sara,
  • Rojas Adriana,
  • Ruiz-Serrano María Jesús,
  • Sánchez Mar,
  • Sanz-Pérez Amadeo,
  • Serrano Julia,
  • Tejerina Francisco,
  • Valerio Maricela,
  • Veintimilla Mª Cristina,
  • Vesperinas Lara,
  • Vicente Teresa,
  • de la Villa Sofía

摘要

There is limited data on the efficacy of combined antiviral treatment for immunosuppressed COVID-19 patients. We describe the clinical and microbiological outcomes of a cohort of oncohaematological patients with persistent SARS-CoV-2 infection who received different dual and triple antiviral combination treatments. We selected the 15 patients (two of them with two episodes) who were prescribed combined anti-SARS-CoV-2 treatment in our institution (October 2021–December 2024). Combined antiviral therapy was administered as a compassionate use in the following indications: (i) persistence of SARS-CoV-2 positive quantitative RT-PCR (qRT-PCR) for > 14 days despite antiviral monotherapy and severe COVID-19 or (ii) need to achieve viral clearance before hematopoietic progenitor transplantation or administration of immuno-chemotherapy. Samples corresponding to positive qRT-PCR results with a Ct value < 32 were analysed by whole-genome sequencing. In 13 out of a total of 15 episodes, with control qRT-PCR after the combination therapy, with positivity periods ranging from 12 to 235 days, viral clearance was achieved 10–69 days after receiving the combination therapy. Whole genome sequencing revealed the emergence of resistance mutations in three cases prior to combination therapy. The therapy was able to overcome these mutations and lead to clearance. Genomic analysis identified one patient with three consecutive reinfections that had been mismanaged as persistent infection. In conclusion, combined antiviral treatment leads to satisfactory clinical and microbiological outcomes in a small cohort of immunocompromised patients with persistent SARS-CoV-2 infection. Early monotherapy treatment in these patients was associated with a high rate of clinical and microbiological failure, with sporadic documentation of resistance mutations that were overcome with combined antiviral therapy.