Abstract
The number of long-term survivors of allogeneic hematopoietic stem cell transplantation (allo-HSCT) is increasing; however, few studies have addressed their long-term pulmonary function. METHODS: The authors examined 660 baseline and follow-up pulmonary function tests in 89 long-term survivors of pediatric hematologic malignancies and allo-HSCT. RESULTS: At least 1 abnormal lung parameter was seen in 40.4% of baseline tests and developed in 64% of post-allo-HSCT tests (median follow-up: 8.9 years). Abnormal baseline values in ratio of forced expiratory volume in 1 second and forced vital capacity (FEV1/FVC), FEV1, residual volume (RV), functional residual capacity (FRC), and FVC were associated with abnormal post-allo-HSCT values. The following pulmonary function values declined significantly with time: FEV1/FVC, forced mid-expiratory flow (FEF25%-75%), total lung capacity (TLC), diffusion capacity corrected for hemoglobin (DLCO corr), RV, FRC, and RV/TLC. Older age at the time of allo-HSCT was associated with lower FEV1/FVC, FEF25%-75%, and DLCOcorr and higher RV/TLC. Patients who experienced respiratory events within 1 year post-allo-HSCT had lower FEV1 and FVC values and higher RV/TLC from their baseline pulmonary function tests. Female patients had reduced FVC, TLC, and RV values but higher FEV1/FVC. Pulmonary dysfunction was also associated with high-risk hematological malignancies and peripheral blood HSC product. CONCLUSIONS: Abnormal pulmonary functions in allo-HSCT survivors are prevalent, which underscore the need for risk-adapted continual monitoring and improved preventive and management strategies.
| Original language | English |
|---|---|
| Pages (from-to) | 2020-2030 |
| Number of pages | 11 |
| Journal | Cancer |
| Volume | 116 |
| Issue number | 8 |
| DOIs | |
| State | Published - Apr 15 2010 |
Keywords
- Childhood
- Hematopoietic stem cell transplantation
- Leukemia
- Pulmonary function
- Survivor
Fingerprint
Dive into the research topics of 'Pulmonary dysfunction in survivors of childhood hematologic malignancies after allogeneic hematopoietic stem cell transplantation'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver