PTCy, Abatacept, and Short Course of Tacrolimus for GvHD Prevention Following Haploidentical Transplantation.
A Samer Al-HomsiFrank CirroneStephanie WoKelli ColeJ Andres Suarez-LondonoSharon L GardnerJingmei HsuKelsey StockerBenedetto BrunoJudith D GoldbergBenjamin A LevinsonMaher Abdul-HayPublished in: Blood advances (2023)
Reducing the incidence of graft-versus host disease (GvHD) following haploidentical hematopoietic stem cell transplantation (HSCT) is warranted. Post-transplant cyclophosphamide (PTCy) is the main agent used for GvHD prevention in this setting. It remains unknown if costimulation blockade can be safely combined with PTCy and enhance its efficacy. We performed a phase Ib-II clinical trial to examine the combination of PTCy, abatacept and a short course of tacrolimus (CAST) following peripheral blood haploidentical HSCT. The primary end-point was the incidence of acute GvHD grades II-IV at day +120. The study enrolled 46 patients with a median age of 60 years (range: 18 to 74). The cumulative incidence of acute GvHD grades II-IV and III-IV was 17.4% (95% CI, 9.2% to 32.9%) and 4.4% (95% CI, 1.1% to 17.1%). With a median follow-up of 15.3 months, the cumulative incidence of one-year treatment-related mortality is 4.4% (95% CI, 1.1% to 17.1%). The estimated one-year chronic GvHD moderate to severe rate, relapse rate, progression-free survival, overall survival, and GvHD- and relapse-free survival were 15.9% (95% CI, 8% to 31.7%), 11.7% (95% CI, 5% to 27.2%), 84.1% (95% CI, 73.8% to 95.7%), 85.9% (95% CI, 75.9% to 97.2%) and 66.1% (95% CI, 53.4% to 81.8%), respectively. Toxicities were similar to those expected in patients receiving haploidentical HSCT. This clinical trial showed that CAST regimen is safe and effective in reducing the rate of grades II-IV acute GvHD following haploidentical peripheral blood HSCT (NCT04503616 at https://clinicaltrials.gov/ct2/show/NCT04503616).
Keyphrases
- peripheral blood
- free survival
- allogeneic hematopoietic stem cell transplantation
- stem cell transplantation
- clinical trial
- risk factors
- liver failure
- bone marrow
- drug induced
- acute myeloid leukemia
- rheumatoid arthritis
- respiratory failure
- hematopoietic stem cell
- acute lymphoblastic leukemia
- cord blood
- magnetic resonance imaging
- study protocol
- low dose
- magnetic resonance
- coronary artery disease
- mesenchymal stem cells
- computed tomography
- randomized controlled trial
- intensive care unit
- high intensity
- pet ct
- systemic lupus erythematosus
- double blind
- contrast enhanced
- stem cells
- smoking cessation