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Thiotepa/cyclophosphamide/TBI as a conditioning regimen for allogeneic hematopoietic stem cell transplantation in patients aged 50 years and over. | LitMetric

AI Article Synopsis

  • The study aimed to reduce relapse rates in hematological malignancies post-transplant using a specific high-intensity chemotherapy and radiation regimen.
  • Seventeen patients, mainly around 53 years old, underwent allogeneic stem cell transplants with a focus on preventing acute graft-versus-host disease (GVHD) through various drug combinations.
  • The treatment showed tolerability with a 59% survival rate after three years, although several patients faced acute and chronic GVHD, and a few died from non-leukemic complications, indicating the need for further research to confirm effectiveness.

Article Abstract

Objective: To reduce the relapse rate for hematological malignancies after allogeneic hematopoietic stem cell transplantation, we employed a myeloablative regimen comprising thiotepa 400 mg/m(2), cyclophosphamide 3,600 mg/m(2) and total body irradiation 10 Gy.

Materials And Methods: Subjects comprised 17 patients (median age, 53 years; range, 50-56 years) with hematological malignancies who received allogeneic hematopoietic stem cell transplantation from HLA-identical related (n=6), HLA-mismatched family (n=2) or unrelated donors (n=9). Prophylaxis of acute graft-versus-host disease (GVHD) consisted of short-term methotrexate and cyclosporine (n=4) or short-term methotrexate and tacrolimus (n=13).

Results: No grade IV regimen-related toxicities as determined by Bearman's criteria were encountered. Acute grade II-IV GVHD developed in 7 patients, with chronic GVHD in 11 patients. With a median follow-up of 39 months, 3 years survival rate after transplantation was 59%. Two patients died due to infection by 100 days after transplantation. Only 1 patient with Philadelphia-positive acute lymphoblastic leukemia experienced relapse. Eight patients died of non-leukemic causes (sepsis, n=2; liver dysfunction, n=2; idiopathic interstitial pneumonia, n=1; bacterial pneumonia, n=1; bronchiolitis obliterans resulting from chronic GVHD, n=1; and disseminated infection with varicella zoster virus, n=1).

Conclusions: This regimen was tolerable, but a large trial is warranted to confirm the efficacy of this conditioning.

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Source
http://dx.doi.org/10.2169/internalmedicine.47.0598DOI Listing

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