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Volume 27, Issue 5, Pages 547-553 (May 2008)


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Rabbit Anti-thymocyte Globulin Induction Therapy Does Not Prolong Survival After Lung Transplantation

Matthew G. Hartwig, MDaCorresponding Author Informationemail address, Laurie D. Snyder, MDb, James Z. Appel III, MDa, Ed Cantu III, MDa, Shu S. Lin, MD, PhDa, Scott M. Palmer, MDb, R. Duane Davis, MDa

Received 8 October 2007; received in revised form 14 January 2008; accepted 24 January 2008.

Background

Lung transplant survival is limited by the development of bronchiolitis obliterans syndrome (BOS). The strongest risk factor for BOS is acute rejection (AR). We have previously shown that rabbit anti-thymocyte globulin (RATG) induction therapy is associated with a decrease in early AR. Thus, we hypothesized that RATG induction would translate to reduced BOS and improved long-term graft survival.

Methods

Forty-four lung recipients were prospectively randomized to receive conventional immunosuppression with RATG induction (RATG group) or conventional immunosuppression alone (control group). End-points included graft survival, early and total acute rejection, BOS and treatment complications.

Results

There was no difference in graft survival between the groups at 8 years (RATG: 36%; control: 23%; p = 0.48). The RATG group had fewer early rejections compared with the control group (5% vs 41%; p = 0.01). However, the overall rejection incidence did not differ (RATG: 62%; control: 68%; p = 0.52). There was a trend toward a delay in BOS onset among RATG subjects compared with control subjects (2,376 days vs 1,108 days; log rank, p = 0.15). There was no difference in the incidence of infections, but the RATG group had a higher rate of malignancies.

Conclusions

Our results suggest that alternative approaches to anti-thymocyte induction should be pursued to reduce BOS and prolong allograft survival.

a Division of Thoracic Surgery, Department of Surgery, Duke University Medical Center, Durham, North Carolina

b Division of Pulmonary and Critical Care Medicine, Department of Medicine, Duke University Medical Center, Durham, North Carolina.

Corresponding Author InformationReprint requests: Department of Surgery, Duke University Medical Center, Box 2605, Medical Science Research Building, Box 2605, Durham, NC 27710. Telephone: 919-684-3705. Fax: 919-681-7263.

PII: S1053-2498(08)00103-4

doi:10.1016/j.healun.2008.01.022


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