Lung transplantation for late-onset non-infectious chronic pulmonary complications of allogenic hematopoietic stem cell transplant

被引:4
作者
Riddell, Peter [1 ,2 ]
Vasudevan-Nampoothiri, Ram [3 ]
Ma, Jin [4 ]
Singer, Lianne G. [1 ,2 ]
Lipton, Jeff H. [3 ]
Juvet, Stephen C. [1 ,2 ]
机构
[1] Toronto Gen Hosp, Ajmera Transplant Ctr, Toronto, ON, Canada
[2] Toronto Gen Hosp, Toronto Lung Transplant Program, Toronto, ON, Canada
[3] Princess Margaret Canc Ctr, Hans Messner Allogen Blood & Marrow Transplant Pr, Toronto, ON, Canada
[4] Univ Toronto, Univ Hlth Network, Biostat Res Unit, Toronto, ON, Canada
关键词
Allogenic hematopoietic stem cell transplantation; Lung transplantation; Infection; BRONCHIOLITIS OBLITERANS; IMMUNE-DEFICIENCY; RISK-FACTORS; OUTCOMES; DISEASE;
D O I
10.1186/s12931-021-01699-8
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background Late onset non-infectious pulmonary complications (LONIPCs) following allogenic hematopoietic stem cell transplantation (allo-HSCT) confer a significant mortality risk. Lung transplantation (LTx) has the potential to provide survival benefit but the impact of prior allo-HSCT on post-LTx outcomes is not well studied. Methods This retrospective, single-centre cohort study assessed the post-LTx outcomes of adults with LONIPCs of allo-HSCT. Outcomes of LTx for LONIPCs were compared to propensity-score matched LTx controls (n = 38, non-HSCT) and recipients of re-LTx (n = 70) for chronic lung allograft dysfunction (CLAD). Results Nineteen patients underwent DLTx for LONIPCs of allo-HSCT between 2003 and 2019. Post-LTx survival was 50% at 5-years. Survival to 1-year post-LTx was similar to matched controls (p = 0.473). Survival, conditional on 1-year survival, was lower in the allo-HSCT cohort (p = 0.034). An increased risk of death due to infection was identified in the allo-HSCT cohort compared to matched controls (p = 0.003). Compared to re-LTx recipients, the allo-HSCT cohort had superior survival to 1-year post-LTx (p = 0.034) but conditional 1-year survival was similar (p = 0.145). Conclusion This study identifies an increased risk of post-LTx mortality in recipients with previous allo-HSCT, associated with infection. It supports the hypothesis that allo-HSCT LTx recipients are relatively more immunosuppressed than patients undergoing LTx for other indications. Optimisation of post-LTx immunosuppressive and antimicrobial strategies to account for this finding should be considered.
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页数:10
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