Donor lymphocyte infusions after haploidentical stem cell transplantation with PTCY: A study on behalf of the EBMT cellular therapy & immunobiology working party
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
36216975
DOI
10.1038/s41409-022-01839-8
PII: 10.1038/s41409-022-01839-8
Knihovny.cz E-zdroje
- MeSH
- cyklofosfamid terapeutické užití MeSH
- imunoterapie adoptivní škodlivé účinky MeSH
- lidé MeSH
- lymfocyty MeSH
- nemoc štěpu proti hostiteli * etiologie MeSH
- prospektivní studie MeSH
- retrospektivní studie MeSH
- transfuze lymfocytů škodlivé účinky MeSH
- transplantace hematopoetických kmenových buněk * škodlivé účinky MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- cyklofosfamid MeSH
Donor lymphocyte infusion (DLI) is a treatment option to prevent or treat relapse after allogeneic hematopoietic cell transplantation (HCT). We here report data for 173 patients who received one or multiple DLIs after haploidentical-HCT with post-transplant cyclophosphamide (PTCY) at 47 EBMT centers from 2009 to 2018. Indication for DLI was: prophylactic for 59 (34.3%), preemptive for 20(11.6%), and therapeutic for 93(54.1%). For the prophylactic group, the median number of DLIs was 1 (IQR:1-2.5) with a median first dose of 0.1 × 106 CD3+ T cell/kg, for the preemptive 2 (IQR:1-3) with 0.5 × 106 CD3+ T cell/kg, for the therapeutic 1 (IQR:1-3) with 1 × 106CD3+ Tcell/kg, respectively. OS after first DLI was 61% (46-75%) for prophylactic, 40% (19-61%) for preemptive, and 22% (13-31%) for therapeutic. CI of II-IV aGVHD and cGVHD was 17% (7-27%) and 53% (40-67%) for the prophylactic, 20% (2-38%) and 21% (3-39%) for the preemptive, 17% (9-24%) and 24% (15-33%) for the therapeutic group, respectively. Our data show great variability in the indications and modalities of DLI across responding EBMT centers. Survival rates remain relatively low in patients with active disease. While the cumulative incidence of aGVHD appears acceptable, we showed a high incidence of cGVHD in the prophylactic group, compared with preemptive and therapeutic DLI. These data should be investigated further in prospective clinical trials.
Anadolu Medical Center Hospital Kocaeli Turkey
Demiroglu Bilim University Istanbul Florence Nightingale Hospital Istanbul Istanbul Turkey
Department of Hematology and Oncology Ospedale Civile Santo Spirito Pescara Italy
EBMT Leiden Study Unit Leiden The Netherlands
EBMT Statistical Unit Leiden The Netherlands
Hospital U Marqués de Valdecilla Santander Spain
Hospital Universitario Reina Sofia IMIBIC University of Cordoba Cordoba Spain
Institute of Hematology and Blood Transfusion Prague Czech Republic
Istituto Clinico Humanitas Milano Italy
Leiden University Medical Center Leiden The Netherlands
Medicana International Hospital Istanbul Istanbul Turkey
RM Gorbacheva Research Institute Pavlov University St Petersburg Russia
San Raffaele Scientific Institute Hematology and Bone marrow Transplantation unit Milan Italy
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