# Successful 30-Day Nirmatrelvir/Ritonavir Treatment of a Patient Who Developed Multi-relapsed COVID-19 After Receiving R-CHOP Against Follicular Lymphoma

**Authors:** Kou Kimoto, Hitoshi Kawasuji, Yoshihiro Yoshida, Hiroshi Yamada, Shunsuke Yazawa, Hideki Tani, Yuki Koshiyama, Yoshimi Nabe, Shohei Kikuchi, Kentaro Nagaoka, Yoshitomo Morinaga, Yoshihiro Yamamoto

PMC · DOI: 10.7759/cureus.79019 · 2025-02-14

## TL;DR

A 58-year-old man with a history of follicular lymphoma experienced multiple relapses of COVID-19, but a 30-day treatment with nirmatrelvir/ritonavir successfully cleared the virus.

## Contribution

This case demonstrates the effectiveness of extended nirmatrelvir/ritonavir treatment in managing prolonged SARS-CoV-2 infection in immunocompromised patients.

## Key findings

- A 30-day nirmatrelvir/ritonavir course resolved symptoms and achieved sustained RT-qPCR negativity.
- Genome analysis confirmed the Omicron BA.5 sublineage BF.13 in cultured and swab samples.
- The patient maintained high neutralizing antibody levels against BA.5 throughout the infection.

## Abstract

A 58-year-old male developed three coronavirus disease 2019 (COVID-19) relapses within three months after rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) chemoimmunotherapy against relapsed follicular lymphoma. Five- and 10-day remdesivir courses failed to achieve viral clearance. A 30-day nirmatrelvir/ritonavir course provided symptom resolution and sustained reverse transcription and quantitative polymerase chain reaction (RT-qPCR) negativity. Genome analyses identified cultured live virus (day 59) and nasopharyngeal-swab viral RNA (days 74, 82, 95) as Omicron BA.5 sublineage BF.13. Normal immunoglobulin (Ig)G levels and high neutralizing activities against BA.5 were maintained throughout the infection's course. Extended nirmatrelvir/ritonavir antiviral treatment may be effective for patients administered anti-CD20 therapy who develop prolonged/relapsed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection despite possessing high neutralizing activities.

## Linked entities

- **Chemicals:** cyclophosphamide (PubChem CID 2907), doxorubicin (PubChem CID 31703), vincristine (PubChem CID 5978), prednisone (PubChem CID 5865), nirmatrelvir (PubChem CID 155903259), ritonavir (PubChem CID 5076)
- **Diseases:** coronavirus disease 2019 (MONDO:0100096), follicular lymphoma (MONDO:0018906)

## Full-text entities

- **Genes:** KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}
- **Diseases:** COVID-19 (MESH:D000086382), infection (MESH:D007239), Follicular Lymphoma (MESH:D008224)
- **Chemicals:** R-CHOP (-), remdesivir (MESH:C000606551), Nirmatrelvir/Ritonavir (MESH:C000719967)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11911031/full.md

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Source: https://tomesphere.com/paper/PMC11911031