Comparable Survival Using A CMV-Matched Or A Mismatched Donor For CMV Plus Patients Undergoing T-Replete Haplo-HSCT With PT-Cy For Acute Leukemia: A Study Of Behalf Of The Infectious Diseases And Acute Leukemia Working Parties Of The EBMT
Tarih
2018Yazar
Cesaro, Simone
Crocchiolo, Roberto
Tridello, Gloria
Knelange, Nina
Van Lint, Maria Teresa
Koc, Yener
Ciceri, Fabio
Gulbas, Zafer
Tischer, Johanna
Afanasyev, Boris
Bruno, Benedetto
Castagna, Luca
Blaise, Didier
Mohty, Mohamad
Irrera, Giuseppe
Diez-Martin, J. L.
Pierelli, Luca
Pioltelli, Pietro
Arat, Mutlu
Delia, Mario
Fagioli, Franca
Ehninger, Gerhard
Aljurf, Mahmoud
Carella, Angelo Michele
Ozdogu, Hakan
Mikulska, Malgorzata
Ljungman, Per
Nagler, Arnon
Styczynski, Jan
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The role of donor CMV serostatus in the setting of non T-cell depleted haplo-HSCT with post-transplant cyclophosphamide (PT-Cy) has not been specifically addressed so far. Here we analyzed the impact of the donor CMV serological status on the outcome of 983 CMV seropositive (CMV+), acute leukemia patients receiving a first, non T-cell depleted haplo-HSCT registered in the EBMT database. The 1-year NRM was 21.3% (95% CI: 18.4-24.8) and 18.8% (95% CI: 13.8-25.5) in the CMV D+P/R+ and D-/R+ pairs, respectively (p = 0.40). Similarly, 1-year OS was 55.1% (95% CI: 50.1-58.0) and 55.7% (95% CI: 48.0-62.8) in the same groups (p = 0.50). The other main outcomes were comparable. No difference in NRM nor OS was observed after stratification for the intensity of conditioning and multivariate anaysis confirmed the lack of significant association with NRM or OS. In conclusion, the choice of a CMV-seronegative donor did not impair early survival of CMV-seropositive patients with acute leukemia after a first, non T-cell depleted haploidentical HSCT and PT-Cy among this series of 983 consecutive patients. Future research may focus on the assessment of the hierarchy of all the donor variables.