Kadono Yoshifumi, Konaka Hiroyuki, Izumi Kouji, Anai Satoshi, Fujimoto Kiyohide, Ishibashi Kei, Kawai Noriyasu, Kato Taku, Iba Akinori, Masumori Naoya, Yoshimura Kenichi, Mizokami Atsushiu
Department of Integrative Cancer Therapy and Urology, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan.
Department of Urology, Nara Medical University, Kashihara-Shi, Nara, Japan.
Contemp Clin Trials Commun. 2019 Jun 26;15:100403. doi: 10.1016/j.conctc.2019.100403. eCollection 2019 Sep.
Appropriate protocol for the sequential treatment of metastatic renal cell carcinoma (mRCC) has not been established yet. Some mRCC cases with favorable risk were reported to achieve complete remission and durable response using interferon alfa (IFNα) + low dose interleukin-2 (IL-2). Cytokine therapies may be suitable for some patients with mRCC as first-line therapy. The present study is a phase III, investigator-initiated, multicenter, prospective randomized controlled trial investigating patients with low and intermediate risk mRCC classified by Memorial Sloan-Kettering Cancer Center risk criteria to evaluate the efficacy and safety of sequential treatment with cytokine (IFNα + IL-2) as first-line and axitinib as second-line therapy versus sequential treatment with sunitinib as first-line and axitinib as second-line therapy, which is the current standard treatment for patients with favorable risk. The target sample size was set at 72 patients per group (total 144 cases). The study duration is 7 years, and the duration for recruitment is 4 years. Our expectation of this trial is to clarify first- and second-line sequential treatment for mRCC better, especially in patients with favorable risk and some with intermediate risk. The results of this trial will certainly contribute to new information for the strategy of first- and second-line sequential treatment for mRCC.
University hospital Medical Information Network (UMIN) Center identifier UMIN 000012522.
转移性肾细胞癌(mRCC)序贯治疗的合适方案尚未确立。据报道,一些低危mRCC病例使用干扰素α(IFNα)+低剂量白细胞介素-2(IL-2)可实现完全缓解和持久反应。细胞因子疗法可能适合部分mRCC患者作为一线治疗。本研究是一项由研究者发起的III期多中心前瞻性随机对照试验,针对根据纪念斯隆凯特琳癌症中心风险标准分类的低危和中危mRCC患者,评估细胞因子(IFNα+IL-2)一线治疗和阿昔替尼二线治疗的序贯疗法与舒尼替尼一线治疗和阿昔替尼二线治疗的序贯疗法(这是目前低危患者的标准治疗方案)的疗效和安全性。目标样本量设定为每组72例患者(共144例)。研究为期7年,招募期为4年。我们期望通过这项试验能更好地明确mRCC的一线和二线序贯治疗方案,尤其是在低危患者以及部分中危患者中。本试验结果必将为mRCC一线和二线序贯治疗策略提供新信息。
大学医院医学信息网络(UMIN)中心标识符UMIN 000012522。