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Optimizing cytomegalovirus treatment through therapeutic drug monitoring in a ganciclovir-unresponsive lung transplant recipient.

Publication ,  Journal Article
Umemura, K; Katada, Y; Katsube, Y; Hira, D; Tsuda, M; Nakagawa, S; Shima, C; Matsumoto, A; Ohsumi, A; Date, H; Nagao, M; Terada, T
Published in: J Infect Chemother
April 2025

Ganciclovir and valganciclovir are utilized in the treatment of cytomegalovirus infection and its reactivation following lung transplantation. However, treatment complexity arises due to the development of resistant viruses. Recently, therapeutic drug monitoring of ganciclovir has been studied to enhance dosing strategies for both ganciclovir and valganciclovir. We present a case of a lung transplant recipient who developed cytomegalovirus infection and diarrhea despite valganciclovir prophylaxis. Therapeutic drug monitoring confirmed that the area under the curve of ganciclovir was 67.0 μg h/mL, indicating adequate drug absorption. Although genotypic sequencing tests for antiviral resistance to cytomegalovirus were unavailable at our institution, our therapeutic drug monitoring findings raised suspicion of ganciclovir resistance in the cytomegalovirus. Therefore, the antiviral regimen was modified to foscarnet, leading to prompt cytomegalovirus clearance. Subsequently, foscarnet was replaced with letermovir for secondary prophylaxis. Throughout the treatment, tests for cytomegalovirus DNA and pp65 antigens consistently yielded negative results. This case underscores the value of therapeutic drug monitoring in suspecting potential ganciclovir resistance.

Duke Scholars

Published In

J Infect Chemother

DOI

EISSN

1437-7780

Publication Date

April 2025

Volume

31

Issue

4

Start / End Page

102686

Location

Netherlands

Related Subject Headings

  • Valganciclovir
  • Transplant Recipients
  • Quinazolines
  • Microbiology
  • Lung Transplantation
  • Humans
  • Ganciclovir
  • Foscarnet
  • Drug Resistance, Viral
  • Drug Monitoring
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Umemura, K., Katada, Y., Katsube, Y., Hira, D., Tsuda, M., Nakagawa, S., … Terada, T. (2025). Optimizing cytomegalovirus treatment through therapeutic drug monitoring in a ganciclovir-unresponsive lung transplant recipient. J Infect Chemother, 31(4), 102686. https://doi.org/10.1016/j.jiac.2025.102686
Umemura, Keisuke, Yoshiki Katada, Yurie Katsube, Daiki Hira, Masahiro Tsuda, Shunsaku Nakagawa, Chiaki Shima, et al. “Optimizing cytomegalovirus treatment through therapeutic drug monitoring in a ganciclovir-unresponsive lung transplant recipient.J Infect Chemother 31, no. 4 (April 2025): 102686. https://doi.org/10.1016/j.jiac.2025.102686.
Umemura K, Katada Y, Katsube Y, Hira D, Tsuda M, Nakagawa S, et al. Optimizing cytomegalovirus treatment through therapeutic drug monitoring in a ganciclovir-unresponsive lung transplant recipient. J Infect Chemother. 2025 Apr;31(4):102686.
Umemura, Keisuke, et al. “Optimizing cytomegalovirus treatment through therapeutic drug monitoring in a ganciclovir-unresponsive lung transplant recipient.J Infect Chemother, vol. 31, no. 4, Apr. 2025, p. 102686. Pubmed, doi:10.1016/j.jiac.2025.102686.
Umemura K, Katada Y, Katsube Y, Hira D, Tsuda M, Nakagawa S, Shima C, Matsumoto A, Ohsumi A, Date H, Nagao M, Terada T. Optimizing cytomegalovirus treatment through therapeutic drug monitoring in a ganciclovir-unresponsive lung transplant recipient. J Infect Chemother. 2025 Apr;31(4):102686.
Journal cover image

Published In

J Infect Chemother

DOI

EISSN

1437-7780

Publication Date

April 2025

Volume

31

Issue

4

Start / End Page

102686

Location

Netherlands

Related Subject Headings

  • Valganciclovir
  • Transplant Recipients
  • Quinazolines
  • Microbiology
  • Lung Transplantation
  • Humans
  • Ganciclovir
  • Foscarnet
  • Drug Resistance, Viral
  • Drug Monitoring