TY - JOUR
T1 - Fludarabine, cyclophosphamide, doxorubicin (FCD), and rituximab
T2 - A remission induction therapy for aggressive pediatric post-transplant lymphoproliferative disease (PTLD)
AU - Giraldi, Eugenia
AU - Provenzi, Massimo
AU - Fiocchi, Roberto
AU - Colledan, Michele
AU - Cornelli, Pieremilio
AU - Torre, Giuliano
AU - Rambaldi, Alessandro
AU - Conter, Valentino
PY - 2011/8
Y1 - 2011/8
N2 - Management of aggressive, usually late-occurring, post-transplant lymphoproliferative disorders (PTLDs), a life-threatening complication after solid organ transplants, remains controversial. Four children affected by aggressive CD20+ PTLDs received a chemo-immunotherapy regimen for remission induction based on fludarabine, cyclophosphamide, doxorubicin, and rituximab, associated with a rapid discontinuation of immunosuppression (IS). Subsequent consolidation chemotherapy consisted of Berlin-Frankfurt-Münster-modified blocks. All patients achieved a complete remission, which persisted for 25, 68+, 80+, and 103+ months after diagnosis. Therapy was well tolerated. No patients developed allograft rejection during PTLD treatment. Our experience suggests that this chemo-immunotherapeutic approach may be an effective treatment strategy while allowing for a concomitant discontinuation of IS.
AB - Management of aggressive, usually late-occurring, post-transplant lymphoproliferative disorders (PTLDs), a life-threatening complication after solid organ transplants, remains controversial. Four children affected by aggressive CD20+ PTLDs received a chemo-immunotherapy regimen for remission induction based on fludarabine, cyclophosphamide, doxorubicin, and rituximab, associated with a rapid discontinuation of immunosuppression (IS). Subsequent consolidation chemotherapy consisted of Berlin-Frankfurt-Münster-modified blocks. All patients achieved a complete remission, which persisted for 25, 68+, 80+, and 103+ months after diagnosis. Therapy was well tolerated. No patients developed allograft rejection during PTLD treatment. Our experience suggests that this chemo-immunotherapeutic approach may be an effective treatment strategy while allowing for a concomitant discontinuation of IS.
KW - Children
KW - Fludarabine-based therapy
KW - PTLD
KW - Rituximab
KW - Solid organ transplantation
KW - Treatment
UR - http://www.scopus.com/inward/record.url?scp=79958858376&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79958858376&partnerID=8YFLogxK
U2 - 10.1002/pbc.23004
DO - 10.1002/pbc.23004
M3 - Article
C2 - 21294246
AN - SCOPUS:79958858376
VL - 57
SP - 324
EP - 328
JO - Pediatric Blood and Cancer
JF - Pediatric Blood and Cancer
SN - 1545-5009
IS - 2
ER -