From Johns Hopkins: Pre-transplant malignancy: An analysis of outcomes after thoracic organ transplantation

http://www.ncbi.nlm.nih.gov/pubmed/23265911

J Heart Lung Transplant. 2012 Dec 19. pii: S1053-2498(12)01391-5. doi: 10.1016/j.healun.2012.11.003. [Epub ahead of print]

Pre-transplant malignancy: An analysis of outcomes after thoracic organ transplantation.

Beaty CA, George TJ, Kilic A, Conte JV, Shah AS.

Source

Division of Cardiac Surgery at the Johns Hopkins Medical Institutions, Baltimore, Maryland.

Abstract

BACKGROUND:

Pre-transplant malignancy (PTM) is a relative contraindication to organ transplantation. Studies examining the effect of PTM on outcomes after lung transplantation (LTx) or orthotopic heart transplantation (OHT) are limited. We evaluated the effect of PTM on outcomes after LTx and OHT.

METHODS:

We retrospectively reviewed primary adult LTx and OHT recipients in the United Network for Organ Sharing database. Primary stratification was by PTM and secondary stratification by tumor type. Matched cohorts (2:1) and multivariable Cox proportional hazards regression models were used to evaluate mortality.

RESULTS:

From 2000 to 2011, 13,613 adults underwent LTx and 19,817 underwent OHT. PTM was present in 740 LTx patients (5.4%) and in 1,117 OHT patients (5.6%). On unadjusted analysis, LTx patients and OHT patients with PTM had similar 30-day, 1-year, and 5-year survivals (p<0.05) compared with patients with no PTM. These findings persisted after risk-adjustment. No tumor types were associated with increased mortality in LTx patients. OHT patients with leukemia, lymphoma, or myeloma (LLM) had a significant increase in univariate mortality at 30 days (hazard ratio [HR], 1.82; p = 0.04), 1 year (HR, 1.93; p<0.001), and 5 years (HR, 1.54; p = 0.01). Matched cohort analysis revealed comparable outcomes in LTx patients but confirmed increased univariate 1-year mortality (HR, 1.89; p = 0.006) in OHT patients with LLM.

CONCLUSIONS:

This large study evaluating the effects of PTM found the incidence of PTM was in LTx 5.4% and in OHT 5.6%. In general, PTM does not increase mortality in either cohort; however, OHT patients with LLM have an increased hazard of mortality. Therefore, carefully selected patients with PTM should not be excluded from LTx or OHT.