Kawamoto Yasuyuki, Komatsu Yoshito, Yuki Satoshi, Sawada Kentaro, Muranaka Tetsuhito, Harada Kazuaki, Nakatsumi Hiroshi, Fukushima Hiraku, Ishiguro Atsushi, Dazai Masayoshi, Hatanaka Kazuteru, Nakamura Michio, Iwanaga Ichiro, Uebayashi Minoru, Sogabe Susumu, Kobayashi Yoshimitsu, Miyagishima Takuto, Ono Kota, Sakamoto Naoya, Sakata Yuh
Department of Cancer Center, Hokkaido University Hospital, Sapporo, Japan.
Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
BMC Cancer. 2017 Dec 8;17(1):837. doi: 10.1186/s12885-017-3850-z.
In Japan, S-1 plus cisplatin (SP) regimen has become a standard therapy for patients with advanced gastric cancer. Moreover, the S-1 plus oxaliplatin regimen is now a standard treatment. Nab-paclitaxel was developed for chemotherapy of gastric cancer in Japanese clinical practice. Nab-paclitaxel, created with albumin-bound paclitaxel particles, has high transferability to tumour tissues and does not cause hypersensitivity reactions because of a different chemical composition compared with docetaxel and paclitaxel. A combination of S-1, nab-paclitaxel and oxaliplatin (which we named 'SNOW regimen') can be a promising triplet therapy for advanced gastric cancer. Although we have to pay attention to chemotherapy-induced neuropathy, we aim to investigate the recommended dose of this regimen in a phase I study. Furthermore, we will investigate its efficacy and toxicity in a phase II study.
The phase I study is a dose-escalation study using a standard 3 plus 3 design, followed by expansion cohorts. The SNOW regimen involves 28-day cycles with escalated doses of nab-paclitaxel (100-175 mg/m on days 1 and 15) and fixed doses of oxaliplatin (65 mg/ m on days 1 and 15) and S-1 (80 mg/m/day on day 1 to 14). The primary endpoints are assessment of dose limiting toxicities and determination of maximum tolerated dose to investigate the recommended dose in the subsequent phase II study. In the phase II study, the primary endpoint is objective response rate. Secondary endpoints are assessment of safety, progression-free survival, disease control rate, overall survival and time to treatment failure. Adverse events were monitored and graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events version 4.0.
Triplet therapies for advanced gastric cancer patients have been evaluated in clinical trials. The SNOW regimen can be a promising new triplet therapy.
This study is performed at institutes that participate in Hokkaido Gastrointestinal Cancer Study Group (HGCSG) and registered as UMIN000016788 . Registrated 16 March 2015.
在日本,S-1联合顺铂(SP)方案已成为晚期胃癌患者的标准治疗方案。此外,S-1联合奥沙利铂方案目前也是一种标准治疗方法。纳米白蛋白结合型紫杉醇在日本临床实践中被用于胃癌化疗。纳米白蛋白结合型紫杉醇由白蛋白结合的紫杉醇颗粒制成,与多西他赛和紫杉醇相比,其化学成分不同,对肿瘤组织具有高转移性且不会引起过敏反应。S-1、纳米白蛋白结合型紫杉醇和奥沙利铂联合方案(我们称之为“SNOW方案”)可能是一种有前景的晚期胃癌三联疗法。尽管我们必须关注化疗引起的神经病变,但我们旨在通过一项I期研究来探究该方案的推荐剂量。此外,我们将在II期研究中探究其疗效和毒性。
I期研究是一项采用标准3 + 3设计的剂量递增研究,随后进行扩大队列研究。SNOW方案包括28天的周期,纳米白蛋白结合型紫杉醇剂量递增(第1天和第15天为100 - 175mg/m²),奥沙利铂固定剂量(第1天和第15天为65mg/m²),S-1(第1天至第14天为80mg/m²/天)。主要终点是评估剂量限制性毒性并确定最大耐受剂量,以探究后续II期研究中的推荐剂量。在II期研究中,主要终点是客观缓解率。次要终点是安全性评估、无进展生存期、疾病控制率、总生存期和治疗失败时间。根据美国国立癌症研究所不良事件通用术语标准第4.0版对不良事件进行监测和分级。
晚期胃癌患者的三联疗法已在临床试验中进行了评估。SNOW方案可能是一种有前景的新三联疗法。
本研究在参与北海道胃肠癌研究组(HGCSG)的机构进行,并注册为UMIN000016788。于2015年3月16日注册。