Department of Oncology, Cliniche Humanitas Gavazzeni, Bergamo, Italy.
Erasmus Medical Center, Rotterdam, Netherlands.
Lancet Oncol. 2019 Dec;20(12):1702-1709. doi: 10.1016/S1470-2045(19)30532-7. Epub 2019 Oct 15.
Tumour Treating Fields (TTFields) are a regional, antimitotic treatment for solid tumours, which is based on the delivery of low-intensity alternating electric fields. The aim of the STELLAR study was to test the activity of TTFields delivered to the thorax in combination with systemic chemotherapy for the front-line treatment of patients with unresectable malignant pleural mesothelioma.
STELLAR was a prospective, single-arm, phase 2 trial done at 12 European academic and non-academic sites (five in Italy, three in Poland, one in France, one in Belgium, one in Spain, and one in the Netherlands) for treatment-naive patients with histologically confirmed unresectable malignant pleural mesothelioma. Patients were aged at least 18 years, had an Eastern Cooperative Oncology Group performance status of 0-1, and at least one measurable or evaluable lesion according to modified Response Evaluation Criteria in Solid Tumors for mesothelioma. Patients received continuous TTFields at a frequency of 150 kHz to the thorax and concomitant chemotherapy with intravenous pemetrexed (500 mg/m on day 1) plus intravenous platinum (either cisplatin 75 mg/m on day 1 or carboplatin area under the curve 5 on day 1) every 21 days for up to six cycles. Patients not progressing after completion of chemotherapy received TTFields as maintenance treatment until progression, patient or physician decision, or unacceptable toxic effects. The primary endpoint of the trial was overall survival. Survival analyses were done in the intention-to-treat population, and safety analyses were done in all patients who received at least 1 day of TTFields treatment. This trial is registered with ClinicalTrials.gov, NCT02397928.
Between Feb 9, 2015 and March 21, 2017, 80 patients were enrolled in the study. Median follow-up was 12·5 months (IQR 7·4-16·6). Median overall survival was 18·2 months (95% CI 12·1-25·8). The most common grade 3 or worse adverse events were anaemia (nine [11%] patients), neutropenia (seven [9%]), and thrombocytopenia (four [5%]). Skin reaction was the only adverse event associated with TTFields and was reported as grade 1-2 in 53 (66%) patients, and as grade 3 in four (5%) patients. No treatment-related deaths were observed.
The trial showed encouraging overall survival results, with no increase in systemic toxicity. TTFields (150 kHz) delivered to the thorax concomitant with pemetrexed and platinum was an active and safe combination for front-line treatment of unresectable malignant pleural mesothelioma. Further investigation in a randomised trial is warranted.
Novocure.
肿瘤治疗电场(TTFields)是一种局部抗有丝分裂的治疗方法,适用于实体肿瘤,其原理是利用低强度的交变电场进行治疗。STELLAR 研究旨在测试将 TTFields 应用于胸部联合全身化疗,作为无法切除的恶性胸膜间皮瘤一线治疗的疗效。
STELLAR 是一项在欧洲 12 个学术和非学术中心(意大利 5 个、波兰 3 个、法国 1 个、比利时 1 个、西班牙 1 个、荷兰 1 个)进行的前瞻性、单臂、2 期临床试验,纳入未经治疗的组织学证实无法切除的恶性胸膜间皮瘤患者。患者年龄至少 18 岁,Eastern Cooperative Oncology Group 体能状态评分为 0-1,根据改良的实体瘤反应评价标准(mRECIST)至少有一个可测量或可评估的病灶。患者接受胸部 TTFields 治疗,频率为 150 kHz,同时接受培美曲塞静脉注射(第 1 天 500 mg/m2)联合顺铂(第 1 天 75 mg/m2)或卡铂(第 1 天 AUC5),每 21 天为一个周期,最多 6 个周期。化疗结束后无进展的患者继续接受 TTFields 维持治疗,直至疾病进展、患者或医生决定、或出现不可耐受的毒性。该试验的主要终点是总生存期。生存分析在意向治疗人群中进行,安全性分析在所有接受至少 1 天 TTFields 治疗的患者中进行。该试验在 ClinicalTrials.gov 注册,编号为 NCT02397928。
2015 年 2 月 9 日至 2017 年 3 月 21 日,共有 80 名患者入组该研究。中位随访时间为 12.5 个月(IQR 7.4-16.6)。中位总生存期为 18.2 个月(95%CI 12.1-25.8)。最常见的 3 级或更高级别的不良事件是贫血(9 例[11%])、中性粒细胞减少(7 例[9%])和血小板减少(4 例[5%])。皮肤反应是唯一与 TTFields 相关的不良事件,53 例(66%)患者报告为 1-2 级,4 例(5%)患者报告为 3 级。未观察到与治疗相关的死亡。
该试验显示出令人鼓舞的总生存期结果,且未增加全身毒性。TTFields(150 kHz)联合培美曲塞和铂类药物应用于胸部,作为无法切除的恶性胸膜间皮瘤的一线治疗是一种有效且安全的联合治疗方法。需要进一步在随机试验中进行研究。
Novocure。