Frontiers in Oncology (Jul 2023)

Diffuse alveolar hemorrhage after hematopoietic cell transplantation- response to treatments and risk factors for mortality

  • Michelle L. Schoettler,
  • Christopher E. Dandoy,
  • Anora Harris,
  • Marilynn Chan,
  • Keiko M. Tarquinio,
  • Sonata Jodele,
  • Muna Qayed,
  • Benjamin Watkins,
  • Pradip Kamat,
  • Toni Petrillo,
  • Jeremy Obordo,
  • Christine S. Higham,
  • Christopher C. Dvorak,
  • Adrianna Westbrook,
  • Matt S. Zinter,
  • Matt S. Zinter,
  • Kirsten M. Williams

DOI
https://doi.org/10.3389/fonc.2023.1232621
Journal volume & issue
Vol. 13

Abstract

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Diffuse alveolar hemorrhage (DAH) is a life-threatening complication of hematopoietic cellular therapy (HCT). This study aimed to evaluate the effect of DAH treatments on outcomes using data from consecutive HCT patients clinically diagnosed with DAH from 3 institutions between January 2018-August 2022. Endpoints included sustained complete response (sCR) defined as bleeding cessation without recurrent bleeding, and non-relapse mortality (NRM). Forty children developed DAH at a median of 56.5 days post-HCT (range 1-760). Thirty-five (88%) had at least one concurrent endothelial disorder, including transplant-associated thrombotic microangiopathy (n=30), sinusoidal obstructive syndrome (n=19), or acute graft versus host disease (n=10). Fifty percent had a concurrent pulmonary infection at the time of DAH. Common treatments included steroids (n=17, 25% sCR), inhaled tranexamic acid (INH TXA,n=26, 48% sCR), and inhaled recombinant activated factor VII (INH fVIIa, n=10, 73% sCR). NRM was 56% 100 days after first pulmonary bleed and 70% at 1 year. Steroid treatment was associated with increased risk of NRM (HR 2.25 95% CI 1.07-4.71, p=0.03), while treatment with INH TXA (HR 0.43, 95% CI 0.19- 0.96, p=0.04) and INH fVIIa (HR 0.22, 95% CI 0.07-0.62, p=0.005) were associated with decreased risk of NRM. Prospective studies are warranted to validate these findings.

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