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同种异体干细胞移植治疗肾细胞癌。

Allogeneic stem cell transplantation for renal cell carcinoma.

机构信息

Department of Hematology, Istituto Scientifico San Raffaele, Via Olgettina 60, 20132 Milano, Italy.

出版信息

Expert Rev Anticancer Ther. 2011 Jun;11(6):901-11. doi: 10.1586/era.11.12.

Abstract

Allogeneic hematopoietic stem cell transplantation from a compatible donor has been utilized as adoptive immunotherapy in metastatic, cytokine-refractory renal cell carcinoma (RCC). Since the year 2000, several investigators have established that RCC is susceptible to a graft-versus-tumor effect: they reported that patients with renal cancer may have partial or complete disease responses, in the 20-40% range, after allogeneic transplantation following a reduced-intensity regimen. However, transplant-related mortality is still high in the 10-20% range, and responses are rarely durable. Experimental evidence suggests that donor-derived T cells and natural killer cells are the main mediators of the graft-versus-RCC effect upon allogeneic hematopoietic stem-cell transplantation. Isolation of CD8(+) cytotoxic T lymphocyte clones recognizing several target antigens of graft-versus-RCC effect (minor histocompatibility antigens on RCC cells; a peptide epitope derived from human endogenous retrovirus type E; the tumor-associated antigen encoded by the Wilms' tumor 1 gene) has increased our knowledge of the disease and has opened up the possibility of antigen-specific adoptive cell therapy. The introduction in the clinic of molecularly targeted agents that interfere with neoangiogenesis, both monoclonal antibodies and small tyrosine-kinase inhibitor molecules (e.g., sunitinib, sorafenib and bevacizumab), has decreased the use of allogeneic transplantation. Although not curative, novel targeted agents may be combined with allogeneic transplantation or with adoptive cell therapy in order to maximize the chances of cure.

摘要

异体造血干细胞移植(来自于相容供者)已被应用于转移性、细胞因子难治性肾细胞癌(RCC)的过继免疫治疗。自 2000 年以来,一些研究人员已经证实 RCC 易受到移植物抗肿瘤效应的影响:他们报告称,接受低强度预处理方案的异体移植后,20%至 40%的肾细胞癌患者可能会出现部分或完全疾病缓解。然而,移植相关死亡率仍高达 10%至 20%,且缓解通常不持久。实验证据表明,在异体造血干细胞移植后,供体来源的 T 细胞和自然杀伤细胞是移植物抗 RCC 效应的主要介导者。分离识别几种移植物抗 RCC 效应靶抗原(RCC 细胞上的次要组织相容性抗原;来源于人类内源性逆转录病毒型 E 的肽表位;Wilms 瘤 1 基因编码的肿瘤相关抗原)的 CD8+细胞毒性 T 淋巴细胞克隆,增加了我们对疾病的认识,并为抗原特异性过继细胞治疗开辟了可能性。临床上引入了干扰新生血管生成的分子靶向药物,包括单克隆抗体和小分子酪氨酸激酶抑制剂(如舒尼替尼、索拉非尼和贝伐单抗),减少了异体移植的应用。尽管不能治愈,但新型靶向药物可能与异体移植或过继细胞治疗联合使用,以最大限度地提高治愈的机会。

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