TY - JOUR
T1 - Low-dose acyclovir prophylaxis for the prevention of herpes simplex virus disease after allogeneic hematopoietic stem cell transplantation
AU - Kawamura, K.
AU - Wada, H.
AU - Yamasaki, R.
AU - Ishihara, Y.
AU - Sakamoto, K.
AU - Ashizawa, M.
AU - Sato, M.
AU - Machishima, T.
AU - Terasako, K.
AU - Kimura, S. I.
AU - Kikuchi, M.
AU - Nakasone, H.
AU - Yamazaki, R.
AU - Kanda, J.
AU - Kako, S.
AU - Tanihara, A.
AU - Nishida, J.
AU - Kanda, Y.
PY - 2013/10
Y1 - 2013/10
N2 - Background: Currently, acyclovir (ACV) at 1000 mg/day is widely used as prophylaxis in the early phase of hematopoietic stem cell transplant (HSCT) in Japan. However, low-dose ACV (200 mg/day) has been shown to prevent varicella zoster virus reactivation in the middle and late phases of HSCT. Methods: Therefore, in this study, we decreased the dose of ACV to 200 mg/day in the early phase after HSCT. We analyzed 93 consecutive herpes simplex virus (HSV)-seropositive patients who underwent allogeneic HSCT for the first time in our center between June 2007 and December 2011. Results: Before August 2009, 38 patients received oral ACV at 1000 mg/day (ACV1000) until day 35 after HSCT, whereas 55 patients received oral ACV at 200 mg/day (ACV200) after September 2009. We compared the cumulative incidence of HSV infection in the 2 groups. Oral ACV was changed to intravenous administration because of intolerance in 66% and 45% of the patients in the ACV1000 and ACV200 groups, respectively (P = 0.060). The probability of severe stomatitis (Bearman grade II-III) was 76% and 60% in the ACV1000 and ACV200 groups, respectively (P = 0.12). The number of patients who developed HSV disease before day 100 after HSCT was 0 in the ACV1000 group and 2 in the ACV200 group, with a cumulative incidence of 3.6% (P = 0.43). HSV disease in the latter 2 patients was limited to the lips and tongue and was successfully treated with ACV or valacyclovir at a treatment dose. Conclusion: ACV at 200 mg/day appeared to be effective for preventing HSV disease in the early phase after HSCT.
AB - Background: Currently, acyclovir (ACV) at 1000 mg/day is widely used as prophylaxis in the early phase of hematopoietic stem cell transplant (HSCT) in Japan. However, low-dose ACV (200 mg/day) has been shown to prevent varicella zoster virus reactivation in the middle and late phases of HSCT. Methods: Therefore, in this study, we decreased the dose of ACV to 200 mg/day in the early phase after HSCT. We analyzed 93 consecutive herpes simplex virus (HSV)-seropositive patients who underwent allogeneic HSCT for the first time in our center between June 2007 and December 2011. Results: Before August 2009, 38 patients received oral ACV at 1000 mg/day (ACV1000) until day 35 after HSCT, whereas 55 patients received oral ACV at 200 mg/day (ACV200) after September 2009. We compared the cumulative incidence of HSV infection in the 2 groups. Oral ACV was changed to intravenous administration because of intolerance in 66% and 45% of the patients in the ACV1000 and ACV200 groups, respectively (P = 0.060). The probability of severe stomatitis (Bearman grade II-III) was 76% and 60% in the ACV1000 and ACV200 groups, respectively (P = 0.12). The number of patients who developed HSV disease before day 100 after HSCT was 0 in the ACV1000 group and 2 in the ACV200 group, with a cumulative incidence of 3.6% (P = 0.43). HSV disease in the latter 2 patients was limited to the lips and tongue and was successfully treated with ACV or valacyclovir at a treatment dose. Conclusion: ACV at 200 mg/day appeared to be effective for preventing HSV disease in the early phase after HSCT.
KW - Acyclovir
KW - Allogeneic hematopoietic stem cell transplantation
KW - Herpes simplex virus disease
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U2 - 10.1111/tid.12118
DO - 10.1111/tid.12118
M3 - Article
C2 - 23895431
AN - SCOPUS:84884977721
SN - 1398-2273
VL - 15
SP - 457
EP - 465
JO - Transplant Infectious Disease
JF - Transplant Infectious Disease
IS - 5
ER -