Division of Cancer Medicine, Department of Cellular Transplantation Biology, Kanazawa University Graduate School of Medical Science, Kanazawa, Ishikawa, Japan.
Jpn J Clin Oncol. 2009 Dec;39(12):807-12. doi: 10.1093/jjco/hyp104. Epub 2009 Sep 20.
Renal cell carcinoma (RCC) is refractory to conventional therapy, including chemotherapy and radiation. However, because RCC is sensitive to cytokine therapy, an immunotherapeutic approach such as hematopoietic stem cell transplantation (HSCT) might lead to a cure. We performed an institutional clinical study of HSCT for refractory RCC patients.
RCC patients aged 50 years or over, refractory to therapy, were eligible for the study. HSCT was performed after reduced-intensity conditioning. Primary endpoint was defined as the survival at day 100 after HSCT with complete donor chimerism, and secondary endpoint was the effectiveness of HSCT.
Seven patients, provided with written informed consent, were enrolled in the study. Six of the seven patients achieved complete donor chimera at day 30 after HSCT, but one patient received second HSCT because of graft rejection. Four patients achieved a partial response (PR) and stable disease was observed in another patient, but these responses were temporary. The disease of the other two patients became progressive. Autopsy findings revealed an accumulation of CD8(+) lymphocytes and degenerative changes in the local RCC lesion in three of six patients who responded clinically. An autopsy of a patient who had obtained a PR revealed lymphocyte involvement with a cytotoxic T cell (CTL) phenotype in the metastasis of RCC.
Our results demonstrate the efficacy of HSCT for RCC and suggest that the graft-versus-tumor effect elicited by CTLs is induced in vivo. HSCT should be further explored as a potential curative treatment for RCC.
肾细胞癌(RCC)对常规治疗(包括化疗和放疗)具有抗性。然而,由于 RCC 对细胞因子治疗敏感,因此造血干细胞移植(HSCT)等免疫治疗方法可能会导致治愈。我们对难治性 RCC 患者进行了 HSCT 的机构临床研究。
年龄在 50 岁或以上、对治疗有抗性的 RCC 患者有资格参加该研究。HSCT 在低强度预处理后进行。主要终点定义为完全供体嵌合体后 100 天 HSCT 的生存率,次要终点是 HSCT 的有效性。
七名患者签署了知情同意书,入组了该研究。七名患者中有六名在 HSCT 后 30 天达到完全供体嵌合体,但有一名患者因移植物排斥而接受了第二次 HSCT。四名患者达到部分缓解(PR),另一名患者观察到疾病稳定,但这些反应是暂时的。另外两名患者的疾病进展。在六名临床反应患者中的三名中,尸检发现局部 RCC 病变中 CD8+淋巴细胞的积累和退行性变化。获得 PR 的患者的尸检显示,RCC 转移中存在具有细胞毒性 T 细胞(CTL)表型的淋巴细胞浸润。
我们的结果表明 HSCT 对 RCC 有效,并提示体内诱导了 CTL 引起的移植物抗肿瘤效应。HSCT 应作为 RCC 的潜在治愈性治疗进一步探索。