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PTCY-Based Haploidentical Donor Transplantation versus HLA-Matched Related and Unrelated Donor Transplantations in Patients with Refractory or Relapsed Lymphoma-A Matched-Pair Analysis. | LitMetric

AI Article Synopsis

  • - Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a promising treatment for patients with recurrent lymphoma, especially with the use of post-transplant cyclophosphamide to prevent graft-versus-host disease (GvHD).
  • - The study compared outcomes of haploidentical HSCT (Haplo-HSCT) with HLA-matched related (MRD) and unrelated donor (URD) transplantations, showing similar survival rates after over 10 years of follow-up, despite 88% of patients having active disease at the start.
  • - Haplo-HSCT showed a significantly lower incidence of acute and chronic GvHD while providing better GvHD-free survival outcomes

Article Abstract

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) has demonstrated its potential as a curative option for patients with r/r lymphoma. With the introduction of post-transplant cyclophosphamide-based (PTCY) graft-versus-host disease (GvHD) prophylaxis, allo-HCT using haploidentical related donors (Haplo-HSCT) has emerged as a valuable alternative for patients without an available HLA-matched donor. In this study, we compared intermediate and long-term outcomes between Haplo-HSCT and HLA-matched related donor (MRD) and unrelated donor (URD) transplantations in 16 matched pairs using age, disease status, lymphoma classification and performance status as matching criteria. Of note, 88% of patients in each group presented with active disease at the time of conditioning. After a median follow-up of >10 years, 10-year overall and progression-free survival and non-relapse mortality incidence after Haplo-HSCT were 31%, 25% and 38%, respectively, and did not differ compared to the values observed in MRD-HSCT and URD-HSCT. A remarkable lower incidence of acute GvHD ≥ II and moderate and severe chronic GvHD was observed after Haplo-HSCT compared to MRD-HSCT (50%/50%, 0.03/0.03) and URD-HSCT (44%/38%, 0.04/0.08), resulting in slightly higher 10-year GvHD-free and relapse-free survival (25%) and chronic GvHD-free and relapse-free survival (25%) in the Haplo-HSCT group. In conclusion, Haplo-HSCT is an effective treatment in patients with non-remission NHL. Given its advantage of immediate availability, haploidentical donors should be preferably used in patients with progressive disease lacking an HLA-matched related donor.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10650710PMC
http://dx.doi.org/10.3390/cancers15215246DOI Listing

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