Valacyclovir for the prevention of cytomegalovirus infection after allogeneic stem cell transplantation: a single institution retrospective cohort analysis

Valacyclovir for the prevention of cytomegalovirus infection after allogeneic stem cell transplantation: a single institution retrospective cohort analysis

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ABSTRACT A retrospective single center study was performed to evaluate the safety and efficacy of valacyclovir for prevention of cytomegalovirus (CMV) infection (reactivation) after


allogeneic stem cell transplantation (SCT). We compared a group of 31 patients at risk for CMV reactivation (donor, recipient or both seropositive for CMV) who received valacyclovir at an


oral dose of 1 g three times a day for CMV prophylaxis with a matched cohort of 31 patients who did not receive the drug or any other form of CMV prophylaxis. Valacyclovir was used as


primary prophylaxis in 12 patients and as secondary prophylaxis (after a prior CMV reactivation was effectively treated with either ganciclovir or foscarnet and without CMV antigenemia at


the start of valacyclovir) in the remaining 19 patients. The two treatment groups were well matched for the donor–recipient CMV serological status and other pre-transplant characteristics.


CMV reactivation was detected by blood antigenemia testing using a commercially available immunofluorescence assay for CMV lower matrix protein pp65 in circulating leukocytes. For primary


prophylaxis, 3/12 patients who received valacyclovir reactivated CMV compared to 24/31 patients in the control group (_P_ < 0.001). For secondary prophylaxis, 5/19 valacyclovir patients


reactivated compared to 16/24 control patients (_P_ < 0.05). Valacyclovir was well tolerated except for infrequent and mild gastrointestinal side-effects. There was no difference in the


incidence of CMV disease in the two groups. Prophylaxis with valacyclovir appears to be safe and efficacious in preventing both primary and secondary CMV reactivation in at-risk patients


after allogeneic SCT. Larger prospective randomized studies will be required to confirm these observations. _Bone Marrow Transplantation_ (2001) 28, 265–270. Access through your institution


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AND AFFILIATIONS * Division of Hematology and Oncology, Department of Medicine, Vanderbilt University School of Medicine and VA Medical Center, Nashville, TN, USA M Vusirikala, SN Wolff, RS


Stein, SJ Brandt, DS Morgan, JP Greer, FG Schuening & SA Goodman * Department of Medicine, and the Division of Infectious Diseases, Department of Medicine, Vanderbilt University School


of Medicine and VA Medical Center, Nashville, TN, USA JS Dummer Authors * M Vusirikala View author publications You can also search for this author inPubMed Google Scholar * SN Wolff View


author publications You can also search for this author inPubMed Google Scholar * RS Stein View author publications You can also search for this author inPubMed Google Scholar * SJ Brandt


View author publications You can also search for this author inPubMed Google Scholar * DS Morgan View author publications You can also search for this author inPubMed Google Scholar * JP


Greer View author publications You can also search for this author inPubMed Google Scholar * FG Schuening View author publications You can also search for this author inPubMed Google Scholar


* JS Dummer View author publications You can also search for this author inPubMed Google Scholar * SA Goodman View author publications You can also search for this author inPubMed Google


Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Vusirikala, M., Wolff, S., Stein, R. _et al._ Valacyclovir for the prevention of cytomegalovirus


infection after allogeneic stem cell transplantation: a single institution retrospective cohort analysis. _Bone Marrow Transplant_ 28, 265–270 (2001). https://doi.org/10.1038/sj.bmt.1703129


Download citation * Received: 18 December 2000 * Accepted: 16 May 2001 * Published: 04 September 2001 * Issue Date: 01 August 2001 * DOI: https://doi.org/10.1038/sj.bmt.1703129 SHARE THIS


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Provided by the Springer Nature SharedIt content-sharing initiative KEYWORDS * cytomegalovirus * valacyclovir * allogeneic SCT