Inferior Outcomes for Patients Developing New-Onset Post-Transplant Diabetes Mellitus after Haploidentical Hematopoietic Cell Transplant
Autor: | Bipin N. Savani, Katie S. Gatwood, Madan Jagasia, Stacey Goodman, Brendan L. Mangan, Adetola A. Kassim, Bhagirathbhai Dholaria, Salyka Sengsayadeth, Dilan A Patel, Wichai Chinratanalab, Heidi Chen, Kathryn A. Culos, Robert F. Cornell, Michael Byrne, Brian G. Engelhardt |
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Rok vydání: | 2020 |
Předmět: |
endocrine system
Transplantation medicine.medical_specialty Hematopoietic cell Cyclophosphamide business.industry Mortality rate Incidence (epidemiology) Cancer Hematology Disease medicine.disease surgical procedures operative hemic and lymphatic diseases Diabetes mellitus Internal medicine medicine Cumulative incidence business medicine.drug |
Zdroj: | Biology of Blood and Marrow Transplantation. 26:S354-S355 |
ISSN: | 1083-8791 |
DOI: | 10.1016/j.bbmt.2019.12.182 |
Popis: | The mortality rate triples for the 50% of patients diagnosed with new-onset post-transplant diabetes mellitus (PTDM) after HLA-identical allogeneic hematopoietic cell transplant (HCT) (Griffith, BBMT 2011). Haploidentical HCT (haplo-HCT) with post-transplant cyclophosphamide (PTCY) is increasingly utilized for patients with hematological disorders but without a conventional HLA-matched donor; however, the effects of PTDM after haplo-HCT is unknown. We examined the incidence, outcomes, and risk factors for PTDM in patients undergoing haplo-HCT. Patients receiving haplo-HCT with PTCY at Vanderbilt-Ingram Cancer Center (n= 65) were retrospectively analyzed for PTDM diagnosis (defined as a random blood glucose ≥200 mg/dL). Exclusion criteria included non-haplo-HCTs, second HCT, or pre-existing diabetes mellitus. The primary outcome was the incidence of new-onset PTDM by day 100. Secondary outcomes included: cumulative incidence (CI) of grades 2-4 graft-versus-host disease (GVHD), time to systemic steroids, PTDM risk factors, overall survival (OS), disease free survival (DFS), and non-relapse mortality (NRM). PTDM was diagnosed in 14 (21.5%) patients at a median of 18 days after haplo-HCT (range, 8-72 days). Hyperglycemia preceded grade 2-4 GVHD and steroids in 12 (85.7%) patents. Clinical characteristics including ablative conditioning and GVHD did not predict PTDM development (Table 1). OS was decreased in the PTDM group (Figure 1). Among haplo-HCT recipients with cancer (n= 41) DFS was lower and the CI of relapse was increased in PTDM patients (Figure 1). Similar to HLA-identical transplants, PTDM occurs frequently, precedes alloreactivity, and leads to inferior survival following haplo-HCT. Interestingly, glucose metabolism appears to be associated with relapse risk. Prophylaxis/treatment of PTDM may improve outcomes after conventional and haplo-HCT. |
Databáze: | OpenAIRE |
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