- Open Access
Tailored total lymphoid irradiation in heart transplant patients: 10-years experience of one center
© Ghadjar et al; licensee BioMed Central Ltd. 2010
- Received: 7 August 2009
- Accepted: 16 January 2010
- Published: 16 January 2010
To assess safety and efficacy of tailored total lymphoid irradiation (tTLI) in cardiac transplant patients.
A total of seven patients, of which five had recalcitrant cellular cardiac allograft rejection (RCCAR), confirmed by endomyocardial biopsies, and two had side effects of immunosuppressive drug therapy, were all treated with tTLI. tTLI was defined by the adjustment of both the fraction interval and the final irradiation dosage both being dependent on the patients general condition, irradiation-dependent response, and the white blood and platelet counts. A mean dose of 6.4 Gy (range, 1.6 - 8.8 Gy) was given. Median follow-up was 7 years (range, 1.8 - 12.2 years).
tTLI was well tolerated. Two patients experienced a severe infection during tTLI (pneumocystis jirovecii pneumonia, urosepsis and generalized herpes zoster) and one patient developed a lymphoproliferative disorder after tTLI. The rate of rejection episodes before tTLI was 0.43 episodes/patient/month and decreased to 0.02 episodes/patient/month after tTLI (P < .001). At the end of the observation time, all patients except one were alive.
tTLI is a useful treatment strategy for the management of RCCAR and in patients with significant side effects of immunosuppressive drug therapy. In this series tTLI demonstrated significantly decreased rejection rates without causing relevant treatment-related toxicity.
- Mycophenolic Mofetil
- Rejection Episode
- White Blood Count
Recalcitrant cellular cardiac allograft rejection (RCCAR) is one of the remaining unsolved problems after heart transplantation (HTx). In case of RCCAR, aggressive up-regulation or adaptation of immunosupression is required, taking additional toxicity into account [1, 2], however, without being sufficient enough to control the rejection process. Total lymphoid irradiation (TLI) for the treatment of RCCAR has been established for over two decades with several published reports demonstrating safety and efficacy of this technique [2–18]. However, little is known about the long term effects after TLI [12, 17]. This study reports on the long-term outcome of seven patients after HTx who received tailored TLI (tTLI) with a median follow-up of 7 years.
Five patients with RCCAR (defined as a rejection grade of IIIA in at least three consecutive endomyocardial biopsies (EMBs) as defined by the International Society for Heart and Lung Transplantation (ISHLT) criteria ) and two patients with severe side effects to immunosuppressive drug treatment were treated by tTLI between February 1996 and January 2006. All patients who underwent HTx at the Swiss Cardiovascular Center, Inselspital, Bern University Hospital received maintenance immunosuppressive therapy with cyclosporine (n = 6), tacrolimus (n = 3), sirolimus (n = 4), prednisone (n = 7), mycophenolic mofetil (n = 5) or azathioprine (n = 4). One patient received a murine antihuman mature T-cell monoclonal antibody (OKT3) for a total of 9 days, 3 weeks prior to tTLI, because of ongoing rejection. All patients received as induction a polyclonal therapy with rATG (Fresenius) during the first 5 days after HTx. Patients were analyzed retrospectively. This study was performed in accordance with the standards of the local ethics committee and with the Helsinki Declaration.
The TLI was performed tailored as previously described . Briefly, patients were treated by three separate fields to encompass all major lymph node bearing areas. A supradiaphragmatic mantle field, a periaortic and splenic field and a pelvic field with inferior extension were used in two patients. The remaining five patients received a supradiaphragmatic mantle field and a inverted Y-field. The non-lymphoid tissue was appropriately shielded in all fields. All fields were treated concurrently on a linear accelerator by an anterior/posterior opposed technique with 6 and 15 MV photons. One patient was treated with a Cobalt 60 source. The prescribed dose was 8 Gy delivered in individual twice weekly 0,8 Gy fractions (calculated midplane dose at central ray). tTLI was performed on a Monday/Thursday or Tuesday/Friday schedule. A control EMB was performed after 2 - 4 fractions. The final decision regarding the dosing was based on the clinical state (e.g. infection), the irradiation-dependent response (efficacy) as well as on the white blood count (WBC) and/or platelet count (Plts) on the day of or one day before planned tTLI. In general tTLI was withheld for a total WBC less than 2.7 thousand/mm3 (or total granulocyte count less than 1.5 thousand/mm3) or Plts less than 125 thousand/mm3 or if Plts were rapidly decreasing.
Descriptives include absolute and relative frequencies for categorical variables and the mean and standard deviation for quantitative variables. The primary objective of this study was to analyze safety and efficacy of tTLI. Secondary objective was to assess long-term survival and toxicity. A severe infection was defined as requiring hospitalisation and/or intravenous antibiotics.
All available WBC, Plts and haemoglobin (Hb) data were collected and analyzed from the time of HTx until 1 year after tTLI. All post-transplant rejection and infection episodes were recorded beginning right after HTx and ending at the end of the follow-up period for each patient. The analysis of tTLI rejection rates was based on calculating the proportion of positive biopsies before and after tTLI and done using an extension of generalized linear models for binomially distributed data using the identity link. Statistical significance was considered on a two-sided level of α = 0.05.
The calculations were performed with the Statistical Analysis Systems (SAS) package (SAS Institute, Cary, NC, USA, version 9.1).
Age at HTx (years)
Dx at HTx
Interval between HTx and tTLI (months)
Duration of tTLI (days)
Number of tTLI courses
tTLI dose (Gy)
4 + 4.8*
1.6 + 6.4+
Evaluation of Safety
Evaluation of Efficacy
Number of rejection episodes before, during and after tTLI
Rejection episodes before tTLI*
Rejection episodes during tTLI*
Rejection episodes after tTLI*
Time to first subsequent rejection episode (months)
Severe Infections during tTLI
The rate of rejection episodes before tTLI was 0.43 episodes/patient/month (95% confidence interval [CI]: 0.31 - 0.58) and decreased to 0.02 episodes/patient/month after tTLI (95% CI: 0.01 - 0.034; P < .001). During the 4 months after tTLI none of the seven patients had further rejection episodes. In the long-term perspective, treatment with tTLI resulted in a decrease of rejection episodes by 28.6% (95% CI: 20.1 - 37.1% decrease). The median time from tTLI to the first subsequent rejection episode was 2.4 years. On average, patients have remained free from acute rejection for 4.1 years (range, 1.4 - 7.8 years).
This study describes long-term safety and efficacy of tTLI in patients who have experienced RCCAR or toxicity of immunosuppressive drug therapy after HTx. In accordance with the literature, describing mainly a non-tailored approach, tTLI was shown to effectively reduce the rejection rate without major treatment related toxicity or infections after a median follow-up of 7 years. Potential long-term risks of tTLI include radiation-induced cardiomyopathy and graft coronary artery disease . The patient who had died from graft coronary artery disease in our series had undergone AB0 mismatched HTx, as previously described . In our series one patient developed a post-transplant lymphoproliferative disorder after he had received OKT3 treatment three weeks prior to the tTLI. The post-transplant lymphoproliferative disorder occurred 2.4 months after completion of tTLI which was diagnosed as an Epstein B Virus (EBV) associated extranodal B-cell lymphoproliferative disease located in the left lung. OKT3 treatment has been shown to be associated with an increased incidence of lymphoproliferative diseases [21, 22]. There however remains a possibility that the lymphoproliferative disorder was attributable to the increased immunosuppression achieved by tTLI. The actuarial risk for post-transplant lymphoproliferative disorder at 5-years after TLI was described to be 9% . It has been demonstrated by others that mTOR-inhibition (S6 kinase pathway), decreases the apoptotic threshold. This may lead to a hypersensitivity of tissues to radiotherapy in patients treated with an mTOR-inhibitor [24, 25]. Since a significant proportion of HTx patients are treated with mTOR inhibitors today, the interaction between mTOR-inhibition and tTLI is an important issue. However, in vitro observations were based on anti-cancer radiation doses, as a consequence the impact of mTOR-inhibition together with the relative low radiation dose used in TLI may not be of clinical importance. In accordance, four of our patients were treated with sirolimus prior to tTLI two of which continued sirolimus during tTLI. In our study there was no difference in WBC or Plts in the patients who received tTLI in combination with sirolimus compared to the patients who received tTLI without sirolimus. Nevertheless, if tTLI is performed in patients on mTOR-inhibitors, careful monitoring is still warranted. The main limitation of this study is that it is a retrospective analysis of a relatively small patient cohort with individually tailored immunosuppressive drug treatment. Our experience has however demonstrated an acceptable safety profile and good efficacy of tTLI which we only instigate in patients with RCCAR already on aggressive immunosuppressive drug treatment or those who cannot tolerate these newer agents (tacrolimus, mycophenolic mofetil and mTOR-inhibitors). We have also demonstrated the feasibility of combined treatment with tTLI and the newer immunosuppressive drugs but recommend careful clinical monitoring.
Based on our center's experience, tTLI is a useful treatment strategy with acceptable safety and good efficacy for both management of RCCAR and for the treatment of patients with limited tolerance to their immunosuppressive drugs after HTx.
We thank Dr. C. Boesch for critically revising our manuscript. This study was supported by the K. Huber-Steiner-Foundation, Bern, Switzerland.
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