Department of Radiation Oncology, University Hospital Bern, Freiburgstrasse, 3010 Bern, Switzerland.
Radiat Oncol. 2010 Jan 16;5:3. doi: 10.1186/1748-717X-5-3.
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.
评估定制性全身淋巴照射(tTLI)在心脏移植患者中的安全性和疗效。
共有 7 名患者,其中 5 名患有经心内膜心肌活检证实的难治性细胞性心脏移植物排斥反应(RCCAR),2 名患有免疫抑制药物治疗的副作用,均接受 tTLI 治疗。tTLI 的定义是根据患者的一般情况、照射依赖性反应以及白细胞和血小板计数来调整分次间隔和最终照射剂量。给予平均剂量 6.4 Gy(范围 1.6-8.8 Gy)。中位随访时间为 7 年(范围 1.8-12.2 年)。
tTLI 耐受良好。2 名患者在 tTLI 期间发生严重感染(卡氏肺孢子虫肺炎、败血症和全身性疱疹),1 名患者在 tTLI 后发生淋巴增生性疾病。tTLI 前排斥反应的发生率为 0.43 次/患者/月,tTLI 后降至 0.02 次/患者/月(P<0.001)。在观察结束时,除 1 名患者外,所有患者均存活。
tTLI 是治疗 RCCAR 和免疫抑制药物治疗有明显副作用患者的有效治疗策略。在本系列中,tTLI 显示出明显降低排斥反应率而没有引起相关的治疗相关毒性。