Bocchi E A, Higuchi M L, Vieira M L, Stolf N, Bellotti G, Fiorelli A, Uip D, Jatene A, Pileggi F
Heart Institute, Medical School of São Paulo University, Brazil.
J Heart Lung Transplant. 1998 Apr;17(4):399-405.
Heart transplantation is a new therapeutic procedure to treat heart failure resulting from Chagas' disease. Experimental studies have demonstrated neoplastic effects of benznidazole, which is used for treatment of Trypanosoma cruzi infection. We compared the incidence and characteristics of neoplasia after heart transplantation for treatment of chronic Chagas' disease with those of other diseases.
Sixteen patients with Chagas' disease and 75 patients with other diseases underwent heart transplantation. Benznidazole was administered to 14 patients with Chagas's disease either for prophylaxis (4 patients) or for treatment of Chagas' disease reactivation (10 patients).
The survival rate of patients in the nonchagasic group was 90% at 1 year and 82.4% at 2 years, and the survival rate in the chagasic group was 63% at 1 year and 57% at 2 years. Six of 16 patients (37.5%) with Chagas' disease had malignant tumors after a mean follow-up time of 25.3+/-2.1 months in contrast to 2 of 75 patients (2.7%) in the nonchagasic group after 34.6+/-3.6 months of follow-up. In the chagasic group, lymphoproliferative disorder was diagnosed in three patients, Kaposi's sarcoma in two, and squamous cell carcinoma in one patient. Reactivation of T. cruzi infection was diagnosed in all patients who had lymphoproliferative disorder. One patient without Chagas' disease had lymphoproliferative disorder in the lung, and another had malignant schwannoma affecting the skin.
We found a higher incidence of malignant neoplasia after heart transplantation for treatment of chronic Chagas' disease. It is likely that the neoplasia is the result of chronic infection with an immunomodulator protozoan, immunosuppression, reactivation of the T. cruzi infection, or the toxicity of therapeutic intervention with benznidazole.
心脏移植是治疗恰加斯病所致心力衰竭的一种新的治疗方法。实验研究已证明用于治疗克氏锥虫感染的苯硝唑具有致瘤作用。我们比较了因慢性恰加斯病接受心脏移植后肿瘤形成的发生率和特征与其他疾病患者的情况。
16例恰加斯病患者和75例其他疾病患者接受了心脏移植。14例恰加斯病患者接受了苯硝唑治疗,其中4例用于预防,10例用于治疗恰加斯病再激活。
非恰加斯病组患者1年生存率为90%,2年生存率为82.4%;恰加斯病组患者1年生存率为63%,2年生存率为57%。16例恰加斯病患者中有6例(37.5%)在平均随访25.3±2.1个月后发生恶性肿瘤,相比之下,非恰加斯病组75例患者中有2例(2.7%)在随访34.6±3.6个月后发生恶性肿瘤。在恰加斯病组中,3例患者被诊断为淋巴增殖性疾病,2例为卡波西肉瘤,1例为鳞状细胞癌。所有发生淋巴增殖性疾病的患者均被诊断为克氏锥虫感染再激活。1例非恰加斯病患者肺部发生淋巴增殖性疾病,另1例患有影响皮肤的恶性神经鞘瘤。
我们发现因慢性恰加斯病接受心脏移植后恶性肿瘤的发生率较高。肿瘤形成可能是免疫调节性原生动物慢性感染、免疫抑制、克氏锥虫感染再激活或苯硝唑治疗干预毒性作用的结果。