PROPHYLACTIC GANCICLOVIR IS MORE EFFECTIVE IN HLA-IDENTICAL FAMILY MEMBER MARROW TRANSPLANT RECIPIENTS THAN IN MORE HEAVILY IMMUNE-SUPPRESSED HLA-IDENTICAL UNRELATED DONOR MARROW TRANSPLANT RECIPIENTS
K. Atkinson et al., PROPHYLACTIC GANCICLOVIR IS MORE EFFECTIVE IN HLA-IDENTICAL FAMILY MEMBER MARROW TRANSPLANT RECIPIENTS THAN IN MORE HEAVILY IMMUNE-SUPPRESSED HLA-IDENTICAL UNRELATED DONOR MARROW TRANSPLANT RECIPIENTS, Bone marrow transplantation, 16(3), 1995, pp. 401-405
A multi-centre Australasian study of the efficacy of prophylactic ganc
iclovir in 88 recipients of marrow allografts at high risk for post-tr
ansplant cytomegalovirus (CMV) disease was conducted. The actuarial in
cidence of CMV disease was 10% in 74 recipients of HLA-identical famil
y member transplants given ganciclovir but was 33% in 14 recipients of
HLA-identical unrelated donor transplants given more immune-suppressi
on pre- and post-transplant (P = 0.006), CMV disease developed in 4 of
the 14 recipients of HLA-identical unrelated donor transplants at a m
edian of 59 days post-transplant and was associated with concurrent gr
aft-versus-host disease (GVHD) in 2 of the 4, CMV disease occurred in
5 of 74 recipients of an HLA-identical family member transplant at a m
edian of 137 days post-transplant and was associated with concurrent m
oderate to severe GVHD in 4 of the 5. Thus the risk of CMV disease was
higher in recipients who were not genotypically identical for HLA wit
h their donors and who (in consequence) were given more immune-suppres
sion than KLA-identical family member transplant recipients. Additiona
lly, CMV disease can occur beyond the period of prophylactic ganciclov
ir administration (first 3 months post-transplant) in patients develop
ing significant chronic GVHD and prophylaxis should be reintroduced at
that time in such patients.