Department of Urology, National Center for Tumor Diseases (NCT), University Hospital Heidelberg, Heidelberg, Germany.
Department of Medical Oncology, National Center for Tumor Diseases (NCT), University Hospital Heidelberg, Heidelberg, Germany.
Urol Int. 2022;106(11):1158-1167. doi: 10.1159/000524097. Epub 2022 Apr 27.
Cytokine-based immunotherapy (IT) has been the mainstay of systemic treatment of advanced renal cell carcinoma (RCC) from the late 1980s until 2007. With the introduction of immune checkpoint inhibitors, a renaissance of immune oncological approaches is rapidly unfolding.
In the present study, we revisited survival outcomes, sexual dimorphism of treatment responses, and the relevance of multimodal treatment approaches over a 30-year period in 156 patients with advanced RCC treated with subcutaneous (s.c.) interleukin-2 (IL-2) and interferon-α (IFN-α) between 1990 and 2009.
The median progression-free survival following the first IT was 5.8 months with a wide range from 0 to 197 months. The median overall survival (OS) was 25.8 months and the median cancer-specific survival after tumor nephrectomy was 24.6 months. A group of 29 patients (18.6%) and 11 patients (7.1%) survived longer than 5 and 10 years after surgery, respectively. A difference in the 5-year OS rate between male and female patients was detected (men, 21.6%; women, 11.1%). However, no sex-specific survival advantage was observed after 10 years.
We provide evidence that IT with s.c. IL-2 and IFN-α played a vital role in long-term survivors either by inducing lasting complete remissions or as part of multimodal approaches that allowed patients to survive until novel therapies became available. The implications for current immune oncological treatment approaches are being discussed.
自 20 世纪 80 年代末至 2007 年,细胞因子为基础的免疫治疗(IT)一直是晚期肾细胞癌(RCC)系统治疗的主要方法。随着免疫检查点抑制剂的引入,免疫肿瘤学方法正在迅速复兴。
在本研究中,我们回顾了在 30 年期间,156 例接受皮下(s.c.)白细胞介素-2(IL-2)和干扰素-α(IFN-α)治疗的晚期 RCC 患者的生存结果、治疗反应的性别差异,以及多模式治疗方法的相关性。这些患者的治疗时间为 1990 年至 2009 年。
首次 IT 后无进展生存期(PFS)的中位数为 5.8 个月,范围从 0 到 197 个月。总生存期(OS)的中位数为 25.8 个月,肿瘤肾切除术的癌症特异性生存期的中位数为 24.6 个月。手术后分别有 29 例(18.6%)和 11 例(7.1%)患者的生存时间超过 5 年和 10 年。男性和女性患者的 5 年 OS 率存在差异(男性,21.6%;女性,11.1%)。然而,在 10 年后没有观察到性别特异性生存优势。
我们提供的证据表明,s.c.IL-2 和 IFN-α 的 IT 通过诱导持久的完全缓解或作为多模式方法的一部分发挥了重要作用,使患者能够存活到新的治疗方法可用。正在讨论这些发现对当前免疫肿瘤学治疗方法的影响。