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Renal cell carcinoma - innovative medical treatments.

机译:肾细胞癌-创新的治疗方法。

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PURPOSE OF REVIEW: This review highlights recent innovations of medical treatments in advanced renal cell carcinoma. Because of significant toxicity many patients do not benefit from standard systemic cytokine therapy using interleukin-2, interferon-alpha, or both. Their median progression-free survival is about 2 months and their overall survival is poor. Here we report improvements in patient outcome, focusing on overall survival, progression-free survival and quality of life to meet their needs. RECENT FINDINGS: Rating treatment results requires analysis of patient selection and risk stratification. In well-selected patients systemic interleukin-2 therapy as well as combinations of cytokines (interleukin-2 and interferon-alpha) improve outcome, induce long-term survival and, in a minority of patients, even produce long-lasting complete remissions. Within the group of patients who are not candidates for systemic cytokines, interleukin-2 for pulmonary metastases given locally by inhalation achieves long-term progression-free survival and long-term overall survival similar to high-dose systemic interleukin-2 but without the toxicity associated with it. In patients at high risk for metastatic disease progression-free survival is prolonged by autologous tumor vaccine as reported in a recent randomized study. However, in established metastatic disease no clear benefit has been demonstrated by any of the many recent vaccine protocols. Chemotherapeutic agents and thalidomide generally fail to improve patient outcome but produce significant and sometimes irreversible toxicity. SUMMARY: Cytokine-based immunotherapy can be considered standard in the treatment of metastatic renal cell carcinoma today. Long-term survival and sometimes even cure seems possible in patients using systemic and local (inhaled) applications of interleukin-2 alone or in combination with interferon-alpha. Noncytokine treatment approaches are scientifically interesting but still disappointing from a patient's perspective.
机译:审查的目的:这篇综述突出了晚期肾细胞癌的医学治疗的最新创新。由于明显的毒性,许多患者无法使用白细胞介素-2,干扰素-α或两者同时使用标准的全身细胞因子治疗。他们的中位无进展生存期约为2个月,总体生存期较差。在这里,我们报告了患者预后的改善,重点是总体生存,无进展生存和满足他们需求的生活质量。最近的发现:对治疗结果进行评级需要分析患者的选择和风险分层。在精选的患者中,系统性白介素2疗法以及细胞因子组合(白介素2和干扰素-α)可改善预后,诱导长期生存,并且在少数患者中,甚至可以产生持久的完全缓解。在非全身性细胞因子候选者的患者组中,通过吸入局部给予的肺转移白介素-2可实现与大剂量全身白介素-2类似的长期无进展生存期和长期总体生存率,但无毒性与之相关。最近的一项随机研究报道,自体肿瘤疫苗可延长转移性疾病高风险患者的无进展生存期。但是,在已确定的转移性疾病中,许多最新的疫苗方案均未显示出明显的益处。化学治疗剂和沙利度胺通常不能改善患者的预后,但会产生明显的,有时是不可逆的毒性。摘要:基于细胞因子的免疫疗法可被认为是当今治疗转移性肾细胞癌的标准方法。单独或与干扰素-α联合使用全身和局部(吸入)白细胞介素2的患者,似乎有可能实现长期生存,甚至治愈。非细胞因子治疗方法在科学上很有趣,但从患者的角度来看仍然令人失望。

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