Shinohara Nobuo, Kumagai Akira, Kanagawa Kouichi, Maruyama Satoru, Abe Takashige, Sazawa Ataru, Nonomura Katsuya
Department of Renal and Genitourinary Surgery, Hokkaido University Graduate School of Medicine, North-15, West-7, Kitaku, Sapporo 060-8638, Japan.
Jpn J Clin Oncol. 2009 Nov;39(11):720-6. doi: 10.1093/jjco/hyp089. Epub 2009 Aug 14.
We conducted a Phase II trial to investigate the efficacy of combined therapy with meloxicam, a cyclooxygenase-2 inhibitor and natural interferon (IFN)-alpha in renal cell carcinoma patients with distant metastasis.
The subjects of this study were patients with untreated renal cell carcinoma who were diagnosed from the results of imaging or pathological studies and who had measurable lesions according to the Response Evaluation Criteria in Solid Tumors (RECIST). Patients could be enrolled in the study irrespective of whether nephrectomy had been performed. Treatment involved the subcutaneous injection of natural IFN-alpha at 3 x 10(6) or 5 x 10(6) U three times weekly plus oral administration of meloxicam at 10 mg once daily.
A total of 43 patients were enrolled in the present study, included 11 patients without nephrectomy, 23 patients with a high C-reactive protein (CRP) level and 23 patients with extrapulmonary metastasis. Four patients of complete response and 12 patients of partial response were confirmed, given an overall response rate of 37.2% (95% confidence interval, 23.0-53.3%). Stable disease for 6 months or longer was also obtained in 14 patients. The median time to progression was 14 months. Adverse events (AEs) observed were mainly flu-like symptoms due to cytokine. Although the Grade 3 or 4 AEs were fatigue, hepatic dysfunction, arthritis and gastric ulcer, all but one (gastric ulcer) were immediately improved by discontinuation of this combined therapy.
The combination of meloxicam and natural IFN-alpha is considered to be an active regimen with tolerable toxicities as a first-line treatment of metastatic renal cell carcinoma.
我们开展了一项II期试验,以研究环氧化酶-2抑制剂美洛昔康与天然α干扰素联合治疗远处转移肾细胞癌患者的疗效。
本研究的受试者为未经治疗的肾细胞癌患者,这些患者通过影像学或病理学检查结果确诊,且根据实体瘤疗效评价标准(RECIST)有可测量病灶。无论是否进行了肾切除术,患者均可纳入本研究。治疗方法为每周皮下注射3×10⁶或5×10⁶单位的天然α干扰素三次,加每日口服10毫克美洛昔康一次。
本研究共纳入43例患者,其中11例未行肾切除术,23例C反应蛋白(CRP)水平较高,23例有肺外转移。确认4例完全缓解,12例部分缓解,总缓解率为37.2%(95%置信区间,23.0 - 53.3%)。14例患者疾病稳定达6个月或更长时间。中位疾病进展时间为14个月。观察到的不良事件(AE)主要是细胞因子引起的流感样症状。虽然3级或4级AE为疲劳、肝功能障碍、关节炎和胃溃疡,但除1例(胃溃疡)外,所有这些不良事件在停用这种联合治疗后均立即得到改善。
美洛昔康与天然α干扰素联合治疗被认为是转移性肾细胞癌一线治疗的一种有效方案,毒性可耐受。