Transplantation Direct (Apr 2021)

Outcomes Following ATG Therapy for Chronic Lung Allograft Dysfunction

  • Sakhee Kotecha, FRACP,
  • Eldho Paul, BS, MS,
  • Steve Ivulich, MPharm,
  • Jeremy Fuller, BS,
  • Miranda Paraskeva, FRACP,
  • Bronwyn Levvey, RN,
  • Gregory Snell, MD, FRACP,
  • Glen Westall, PhD, FRACP

DOI
https://doi.org/10.1097/TXD.0000000000001134
Journal volume & issue
Vol. 7, no. 4
p. e681

Abstract

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Background. Chronic lung allograft dysfunction (CLAD) is the major factor limiting survival post lung transplantation (LTx) with limited effective therapeutic options. We report our 12-y experience of antithymocyte globulin (ATG) as second-line CLAD therapy. Methods. Clinical and lung function data were collected on LTx patients receiving ATG. Rate of FEV1 decline (mL/d) was calculated before and after ATG. Partial response to ATG was defined by rate of FEV1 decline improving 20%. Complete response was defined by an absolute improvement or stability in baseline FEV1. Results. Seventy-six patients received ATG for CLAD. Of these, 5 patients who had a clinical diagnosis of antibody-mediated rejection and were treated with plasmapheresis before or after ATG were excluded from analysis. Sixteen (23%) were complete responders, 29 (40%) were partial responders, and 26 (37%) did not respond. Those with CLAD stage 2 or 3 and younger age were more likely to respond. Partial responders had a 65% lower risk of death or retransplant (HR, 0.35; P = 0.003), whereas complete responders reduced their risk by 70% (HR, 0.30; P = 0.006). Conclusions. ATG appears to stabilize or attenuate lung function decline in CLAD, which may lead to improved retransplant-free survival. Although certain predictors of response have been identified in this large single-center review, these findings need to be confirmed by a multicenter randomized-controlled trial to determine predictors of response to ATG for CLAD.