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Molecularly targeted therapy for Kaposi's sarcoma in a kidney transplant patient: case report,

机译:肾移植患者卡波西肉瘤的分子靶向治疗:病例报告,

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Background Imatinib is a tyrosine-kinase inhibitor; for which there is limited information regarding its effects on AIDS Kaposi's sarcoma and none in patients with transplant-associated Kaposi's sarcoma. Sirolimus, an immunosuppressive drug used for kidney transplant, exhibits antiangiogenic activity related to impaired production of VEGF (vascular endothelial growth factor), clinical benefit has been reported in Kaposi's sarcoma associated with renal graft. Case Presentation Here we report a case of an 80 year old male, who developed Kaposi's Sarcoma nine months after receiving a living non-related donor kidney transplant at age 74. Three years after treatment with different chemotherapeutic agents for progressive cutaneous Kaposi's Sarcoma with no visceral involvement, he was prescribed Imatinib (200 mg/day for two weeks followed by 400 mg/day) after four weeks of treatment he developed anasarca, further progression of KS and agranulocytosis. Imatinib was discontinued and there was significant clinical recovery. One year later his immunosuppressive therapy was changed to Sirolimus and regression of the Kaposi's sarcoma occurred. Conclusion The lack of benefit and severe toxicity associated with the use of Imatinib in this patient should alert clinicians of potentially adverse consequence of its use in patients with transplant associated Kaposi's sarcoma. On the other hand the positive response seen in this patient to Sirolimus even after a long evolution of Kaposi's sarcoma, multiple chemotherapy regimens and extensive cutaneous disease further suggest it therapeutical utility for transplant associated Kaposi's sarcoma.
机译:背景伊马替尼是一种酪氨酸激酶抑制剂。目前,关于其对艾滋病卡波西氏肉瘤的影响的信息有限,在与移植相关的卡波西氏肉瘤的患者中没有任何信息。西罗莫司(Sirolimus)是一种用于肾脏移植的免疫抑制药物,表现出与血管内皮生长因子(VEGF)产生受损有关的抗血管生成活性,据报道在与肾脏移植相关的卡波西氏肉瘤中具有临床益处。病例介绍在这里,我们报告了一个病例,该例为一名80岁男性,他在74岁接受了不相关的供体肾脏活体移植后九个月发展为卡波西氏肉瘤。三年后,用不同的化疗药物治疗了无内脏的进行性皮肤卡波西氏肉瘤受累后,在治疗了四个星期后,他患上了阿那萨卡(anasarca),KS进一步进展和粒细胞缺乏症,接受了伊马替尼(200毫克/天,持续2周,然后是400毫克/天)的处方。伊马替尼停药,临床恢复明显。一年后,他的免疫抑制疗法改为西罗莫司,卡波西氏肉瘤消退。结论该患者缺乏与伊马替尼相关的益处和严重毒性,应提醒临床医生在与移植相关的卡波西氏肉瘤患者中使用伊马替尼有潜在的不良后果。另一方面,即使经过长时间的卡波西氏肉瘤演变,多次化疗方案和广泛的皮肤疾病,该患者对西罗莫司的阳性反应也进一步表明其对移植相关的卡波西氏肉瘤具有治疗作用。

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