4.2 Article

Fluticasone, Azithromycin, and Montelukast Treatment for New-Onset Bronchiolitis Obliterans Syndrome after Hematopoietic Cell Transplantation

期刊

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
卷 22, 期 4, 页码 710-716

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2015.10.009

关键词

Bronchiolitis obliterans syndrome; Fluticasone; Azithromycin; Montelukast; Hematopoietic cell transplantation; Lung chronic graft-versus-host disease; Leukotrienes

资金

  1. NCATS
  2. National Cancer Institute
  3. GlaxoSmithKline [113611]
  4. Grants-in-Aid for Scientific Research [15K19563] Funding Source: KAKEN

向作者/读者索取更多资源

Bronchiolitis obliterans syndrome (BOS) after allogeneic hematopoietic cell transplantation (HCT) is associated with high mortality. We hypothesized that inhaled fluticasone, azithromycin, and montelukast (FAM) with a brief steroid pulse could avert progression of new-onset BOS. We tested this in a phase II, single-arm, open-label, multicenter study (NCT01307462). Thirty-six patients were enrolled within 6 months of BOS diagnosis. The primary endpoint was treatment failure, defined as 10% or greater forced expiratory volume in 1 second decline at 3 months. At 3 months, 6% (2 of 36, 95% confidence interval, 1% to 19%) had treatment failure (versus 40% in historical controls, P < .001). FAM was well tolerated. Steroid dose was reduced by 50% or more at 3 months in 48% of patients who could be evaluated (n = 27). Patient-reported outcomes at 3 months were statistically significantly improved for Short-Form 36 social functioning score and mental component score, Functional Assessment of Cancer Therapies emotional well-being, and Lee symptom scores in lung, skin, mouth, and the overall summary score compared to enrollment (n = 24). At 6 months, 36% had treatment failure (95% confidence interval, 21% to 54%, n = 13 of 36, with 6 documented failures, 7 missing pulmonary function tests). Overall survival was 97% (95% confidence interval, 84% to 100%) at 6 months. These data suggest that FAM was well tolerated and that treatment with FAM and steroid pulse may halt pulmonary decline in new-onset BUS in the majority of patients and permit reductions in systemic steroid exposure, which collectively may improve quality of life. However, additional treatments are needed for progressive BUS despite FAM. (C) 2016 American Society for Blood and Marrow Transplantation.

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