Case Report: Immune-directed post-transplant maintenance with low-dose gemtuzumab ozogamicin and stepwise donor lymphocyte infusion in acute myeloid leukemia with t(1;3)(p36.3;q21)
Aug 2026· Frontiers in Immunology· Vol 17· 0 citations· 34 references
Medicine
TL;DR
This case suggests that sequential low-dose GO followed by stepwise DLI may support durable remission when used as a post-transplant maintenance strategy in chemo-refractory AML with adverse cytogenetics, such as t(1;3)(p36.3;q21).
Abstract
Relapse after allogeneic hematopoietic stem cell transplantation (allo-HSCT) is the leading cause of treatment failure in acute myeloid leukemia (AML), particularly in genetically adverse subtypes. Although prophylactic donor lymphocyte infusion (DLI) may augment graft-versus-leukemia effects, its stand-alone efficacy is suboptimal, necessitating rational combination approaches. Limited case reports have suggested potential clinical benefits of gemtuzumab ozogamicin (GO) in combination with DLI as salvage therapy for post-transplant relapse; however, its role in prophylactic maintenance has not been determined. We report a 29-year-old woman with chemo-refractory AML harboring t(1;3)(p36.3;q21) who relapsed approximately 3 months after her first allo-HSCT. She underwent a second haploidentical allo-HSCT without achieving remission beforehand. Given the extremely high risk of relapse, she received immune-directed maintenance with low-dose GO (3 mg/m2 on days 98 and 140 post-transplant) followed by dose-escalated DLI (six monthly infusions starting on day 374). Although the patient developed chronic graft-versus-host disease, including pulmonary involvement (NIH lung score 2), it remained clinically manageable. She maintained molecular complete remission for more than 6 years. Our case suggests that sequential low-dose GO followed by stepwise DLI may support durable remission when used as a post-transplant maintenance strategy in chemo-refractory AML with adverse cytogenetics, such as t(1;3)(p36.3;q21). This maintenance approach warrants further investigation to clarify feasibility and safety.
Patients with refractory or relapsed T-cell acute lymphoblastic leukemia (R/R T-ALL) have dismal outcomes. While immunotherapies are growing opportunities for B-cell ALL, targeted therapies for T-ALL remain limited. The CD38 antigen, steadily expressed on T-ALL blasts, represents a relevant therapeutic target. Daratumu...
Perrine Moyer, Baptiste Le Calvez, C. Mayeur-Rousse et al.· Pediatric Blood & Cancer· 0 citations
Post-transplant relapsed acute myeloid leukemia (AML) carries a dismal prognosis. Whether gemtuzumab ozogamicin (GO)-containing salvage strategies can achieve sufficient disease control to facilitate second (2nd) allo-HSCT remains unclear. We retrospectively analyzed 34 patients with CD33-positive AML treated with GO-c...
Xiaohong Liu, Long Jing, Xing-Yu Cao et al.· Transplantation and Cellular...· 0 citations
In AML patients receiving alloHSCT with PTCy, outcomes were largely similar regardless of whether CR1 was achieved after one or two-induction courses, with relapse incidence being higher in patients requiring 2 inductions.
A. Nagler, R. Swoboda, Allain-Thibeault Ferhat et al.· Bone Marrow Transplantation· 0 citations
BACKGROUND
Relapse of acute myeloid leukemia (AML) after allogeneic stem cell transplantation (alloSCT) remains a major cause of treatment failure, with poor long-term survival. Donor lymphocyte infusion (DLI) can induce a graft-versus-leukemia effect but may also lead to graft-versus-host disease (GvHD) associated mor...
J. Bergsma, E. Argiro, K. Oosterink et al.· Transplantation and Cellular...· 0 citations
Background Philadelphia chromosome-positive mixed phenotype acute leukemia (Ph+ MPAL) is a rare and aggressive hematologic malignancy. The incorporation of tyrosine kinase inhibitors (TKIs) into acute lymphoblastic leukemia (ALL)-like regimens has improved survival for Ph+ MPAL. However, the benefit of ALL-like chemoth...
Juan Zhang, Yan Huang, Liang-Kui Luo et al.· Frontiers in Medicine· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.