Department of Frontier Science for Cancer and Chemotherapy, Osaka University Graduate School of Medicine, E21-19, 2-2, Yamadaoka, Suita, Osaka, 565-0871, Japan.
Department of Head and Neck, Esophageal Medical Oncology / Department of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Esophagus. 2021 Oct;18(4):835-843. doi: 10.1007/s10388-021-00850-0. Epub 2021 May 16.
In the phase II ATTRACTION-1 study, nivolumab demonstrated a promising antitumor activity among Japanese patients with treatment-refractory advanced esophageal cancer. Here, we report the follow-up results of ATTRACTION-1 of > 5 years.
We enrolled patients with esophageal cancer that was refractory or intolerant to a standard chemotherapy. Then, nivolumab (3 mg/kg) was administered every 2 weeks. The primary endpoint was a centrally assessed objective response rate.
Nivolumab was administered to 65 patients with esophageal squamous-cell carcinoma (ESCC). The centrally assessed objective response rate was 17.2%. The overall survival rates at 3 and 5 years were 10.9% and 6.3%, respectively. Three-year survivors tended to have more reduced target lesions. A total of 63.1% of the patients exhibited treatment-related adverse events, and no new safety signal was observed. Patients with select adverse events tended to have better overall survival than those without. No apparent chronological order was observed between the first response and the onset of select adverse events.
Our follow-up analysis of more than 5 years is currently the longest and is the first to demonstrate that nivolumab has long-term efficacy and safety for advanced ESCC.
在 ATTRACTION-1 期研究中,nivolumab 显示出在治疗难治性晚期食管癌的日本患者中具有良好的抗肿瘤活性。在此,我们报告 ATTRACTION-1 的随访结果超过 5 年。
我们招募了对标准化疗有抗药性或不耐受的食管癌患者。然后,每 2 周给予 nivolumab(3mg/kg)。主要终点是中央评估的客观缓解率。
nivolumab 用于 65 例食管鳞癌(ESCC)患者。中央评估的客观缓解率为 17.2%。3 年和 5 年的总生存率分别为 10.9%和 6.3%。3 年生存者的目标病灶明显减少。共有 63.1%的患者出现与治疗相关的不良反应,未观察到新的安全信号。有选择的不良反应患者的总生存率好于无不良反应的患者。首次反应和选择的不良反应之间没有明显的时间顺序。
我们的随访分析超过 5 年,目前是最长的,也是第一个证明 nivolumab 对晚期 ESCC 具有长期疗效和安全性的研究。