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Late-onset pulmonary complications following allogeneic hematopoietic cell transplantation in pediatric patients: a prospective multicenter study

  • Véronique Houdouin,
  • Jean Christophe Dubus,
  • Sophie Guilmin Crepon,
  • Fanny Rialland,
  • Bénedicte Bruno,
  • Charlotte Jubert,
  • Philippe Reix,
  • Marlène Pasquet,
  • Catherine Paillard,
  • Dalila Adjaoud,
  • Cyril Schweitzer,
  • Muriel Le Bourgeois,
  • Justine Pages,
  • Adyla Yacoubi,
  • Jean Hugues Dalle,
  • Anne Bergeron,
  • Christophe Delclaux

摘要

The primary objective of our multicenter prospective study was to describe the incidence of late-onset non-infectious pulmonary complications (LONIPCs) in children undergoing hematopoietic cell transplantation (HCT) using sensitive criteria for pulmonary function test (PFT) abnormalities including the non-specific pattern of airflow obstruction. Secondary objectives were to assess the factors associated with LONIPC occurrence and the sensitivity of the 2014 NIH-Consensus Criteria of bronchiolitis obliterans syndrome (BOS). PFT and clinical assessment were performed prior to HCT and at 6, 12, 24, and 36 months post-HCT. LONIPC diagnosis was validated by an Adjudication Committee. The study comprised 292 children from 12 centers. Thirty-two individuals (11%, 95% CI: 8–15%) experienced 35 LONIPCs: 25 BOS, 4 interstitial lung diseases, 4 organizing pneumonia and 2 pulmonary veno-occlusive diseases. PFT abnormalities were obstructive defects (FEV1/FVC z-score < −1.645; n = 12), restrictive defects (TLC < 80% predicted, FEV1 and FVC z-scores < −1.645; n = 7) and non-specific pattern (FEV1 and FVC z-score< −1.645, FEV1/FVC z-score > −1.645, and TLC > 80% predicted; n = 8). HCT for malignant disease was the only factor associated with LONIPC (P = 0.04). The 2014 NIH-Consensus Criteria would only diagnose 8/25 participants (32%) as having BOS. In conclusion, 11% of children experienced a LONIPC in a prospective design. Clinical Trials.gov identifier (NCT number): NCT02032381.