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甲氨蝶呤或全淋巴照射治疗持续性或复发性同种异体移植细胞排斥反应:一项比较研究。

Methotrexate or total lymphoid radiation for treatment of persistent or recurrent allograft cellular rejection: a comparative study.

作者信息

Ross H J, Gullestad L, Pak J, Slauson S, Valantine H A, Hunt S A

机构信息

Division of Cardiovascular Medicine, Stanford University School of Medicine, California, USA.

出版信息

J Heart Lung Transplant. 1997 Feb;16(2):179-89.

PMID:9059929
Abstract

BACKGROUND

Methotrexate and total lymphoid irradiation (TLI) have been used successfully for treatment of recurrent and persistent rejection in orthotopic heart transplant recipients; however, there has been no comparison of these two modalities.

METHODS

We retrospectively compared the efficacy of methotrexate (n = 29) versus TLI (n = 28) in heart transplant recipients with recurrent or persistent rejection. All patients received induction therapy (rabbit anti-thymocyte globulin or OKT3) and standard triple immunosuppressive therapy. Methotrexate (7.5 mg to 22.5 mg per wk) or TLI (80 cGy x 10 fractions) was used for the treatment of recurrent or persistent rejection on the basis of clinical indications. Average biopsy scores (International Society of Heart and Lung Transplantation biopsy score/total number of biopsies performed) calculated over 3-month periods, daily maintenance prednisone dose before and after methotrexate or TLI treatment, and actuarial survival and freedom from angiographic coronary artery disease and infection were compared. To control for the general decrease in prednisone with increased time from transplantation, a control group matched for time from transplantation was selected.

RESULTS

Recipient sex and age at transplant, donor age, and donor ischemic time were similar in both groups. Days after transplantation to start of therapy was longer in patients receiving methotrexate; however, this did not reach statistical significance. Patients receiving TLI had received more cumulative corticosteroids and OKT3 before the start of TLI therapy (p < 0.001). There were no differences in actuarial freedom from infection or coronary artery disease between the two groups and between the treatment groups and the control group. Actuarial survival was reduced in patients receiving TLI 3 years after transplantation (p < 0.05). Maintenance prednisone doses from 3 months before until 9 months after therapy (mg/kg) were not different between patients receiving TLI and methotrexate and were significantly greater than the prednisone doses in the control group. Four months after treatment initiation, the prednisone dose was significantly reduced in both treatment groups compared with the pretherapy dose (methotrexate 0.28 +/- 0.16 to 0.22 +/- 0.13, p = 0.05; TLI 0.36 +/- 0.16 to 0.22 +/- .07, p < 0.001). The average biopsy score was significantly reduced by both methotrexate and TLI therapy (methotrexate 1.8 +/- 0.7 to 0.83 +/- 0.9, p = 0.0001; TLI 2.1 +/- 0.8 to 1.0 +/- 0.9, p = 0.0001).

CONCLUSION

Methotrexate and TLI are both effective for the treatment of recurrent or persistent rejection after heart transplantation, reducing average biopsy scores and daily maintenance prednisone doses. There was a reduction in actuarial survival rates in patients treated with TLI, possibly reflecting the greater rejection therapy received before TLI initiation. Because both agents are effective, the choice of methotrexate or TLI may be based on clinical indications, as well as other issues, such as cost, compliance, and availability.

摘要

背景

甲氨蝶呤和全身淋巴照射(TLI)已成功用于治疗原位心脏移植受者的复发和持续性排斥反应;然而,尚未对这两种方法进行比较。

方法

我们回顾性比较了甲氨蝶呤(n = 29)与TLI(n = 28)在心脏移植受者复发或持续性排斥反应中的疗效。所有患者均接受诱导治疗(兔抗胸腺细胞球蛋白或OKT3)和标准三联免疫抑制治疗。根据临床指征,使用甲氨蝶呤(每周7.5毫克至22.5毫克)或TLI(80厘戈瑞×10次分割)治疗复发或持续性排斥反应。比较3个月期间计算的平均活检评分(国际心肺移植学会活检评分/所进行活检的总数)、甲氨蝶呤或TLI治疗前后的每日维持泼尼松剂量以及精算生存率和无血管造影冠状动脉疾病及感染的情况。为控制移植后时间延长导致的泼尼松总体减少,选择了移植后时间匹配的对照组。

结果

两组患者的受者性别、移植时年龄、供者年龄和供者缺血时间相似。接受甲氨蝶呤治疗的患者从移植到开始治疗的天数较长;然而,这未达到统计学显著性。接受TLI治疗的患者在TLI治疗开始前接受了更多的累积皮质类固醇和OKT3(p < 0.001)。两组之间以及治疗组与对照组之间在无感染或冠状动脉疾病的精算自由度方面没有差异。接受TLI治疗的患者在移植后3年的精算生存率降低(p < 0.05)。接受TLI和甲氨蝶呤治疗的患者从治疗前3个月到治疗后9个月的维持泼尼松剂量(毫克/千克)没有差异,且显著高于对照组的泼尼松剂量。治疗开始后4个月,与治疗前剂量相比,两个治疗组的泼尼松剂量均显著降低(甲氨蝶呤从0.28±0.16降至0.22±0.13,p = 0.05;TLI从0.36±0.16降至0.22±0.07,p < 0.001)。甲氨蝶呤和TLI治疗均使平均活检评分显著降低(甲氨蝶呤从1.8±0.7降至0.83±0.9,p = 0.0001;TLI从2.1±0.8降至1.±0.9,p = 0.0001)。

结论

甲氨蝶呤和TLI均对心脏移植后复发或持续性排斥反应有效,可降低平均活检评分和每日维持泼尼松剂量。接受TLI治疗的患者精算生存率有所降低,这可能反映了在开始TLI治疗前接受了更多的抗排斥治疗。由于两种药物均有效,甲氨蝶呤或TLI的选择可基于临床指征以及其他问题,如成本、依从性和可及性。

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