Bonner J A, McGinnis W L, Stella P J, Marschke R F, Sloan J A, Shaw E G, Mailliard J A, Creagan E T, Ahuja R K, Johnson P A
Mayo Clinic and Mayo Foundation, Rochester, Minnesota, USA.
Cancer. 1998 Mar 15;82(6):1037-48.
A three-arm Phase III randomized trial was performed to compare response rates, time to local or distant progression, and survival for patients with unresectable (Stage IIIA or IIIB) nonsmall cell lung carcinoma treated with standard fractionated thoracic radiotherapy (SFTRT) versus accelerated hyperfractionated thoracic radiotherapy (AHTRT) with or without combination etoposide and cisplatin chemotherapy.
This trial was initiated in 1992 by the North Central Cancer Treatment Group. Patients with Stage IIIA or IIIB nonsmall cell lung carcinoma were eligible. They were randomly assigned to either SFTRT (6000 centigray [cGy] in 30 fractions) or AHTRT (150 cGy twice daily to a total dose of 6000 cGy, with a 2-week break after the initial 3000 cGy); the AHTRT was given alone or with concomitant cisplatin (30 mg/m2, Days 1-3 and 28-30) and etoposide (100 mg/m2, Days 1-3 and 28-30).
A total of 110 patients were entered on study. Eleven patients were declared ineligible or off study on the day of study entry. This analysis was confined to the 99 eligible patients. This article reports mature follow-up, because more than 80% of the patients have died. The median follow-up of living patients was 2.5 years. There were suggestions of improvement in the rates of freedom from local recurrence and survival for patients treated with AHTRT (with or without chemotherapy) as opposed to SFTRT (P = 0.06 and P = 0.10, respectively). The improvement in survival associated with AHTRT (with or without chemotherapy) was statistically significant for the subgroup of patients with nonsquamous cell carcinoma after adjustment for other potentially confounding factors (P = 0.02). No differences in freedom from systemic progression or survival were found in a comparison of AHTRT with chemotherapy and AHTRT without chemotherapy.
These results suggest that treatment of Stage IIIA or IIIB nonsmall cell lung carcinoma with AHTRT with or without chemotherapy may improve freedom from local progression and survival as compared with SFTRT, especially for patients with nonsquamous cell carcinoma. The statistical powers to detect the observed differences in median time to local progression and survival were approximately 55% and 35%, respectively. Therefore, further investigation comparing SFTRT with AHTRT is warranted.
开展了一项三臂III期随机试验,比较不可切除(IIIA期或IIIB期)非小细胞肺癌患者接受标准分割胸部放疗(SFTRT)与加速超分割胸部放疗(AHTRT)联合或不联合依托泊苷和顺铂化疗时的缓解率、局部或远处进展时间及生存率。
该试验由北中部癌症治疗组于1992年启动。IIIA期或IIIB期非小细胞肺癌患者符合条件。他们被随机分配至SFTRT组(30次分割,总剂量6000厘戈瑞[cGy])或AHTRT组(每日两次,每次150 cGy,总剂量6000 cGy,初始3000 cGy后休息2周);AHTRT可单独使用,或联合顺铂(30 mg/m²,第1 - 3天和第28 - 30天)及依托泊苷(100 mg/m²,第1 - 3天和第28 - 30天)。
共有110例患者进入研究。11例患者在研究入组当天被判定不符合条件或退出研究。本分析仅限于99例符合条件的患者。本文报告了成熟的随访结果,因为超过80%的患者已死亡。存活患者的中位随访时间为2.5年。与SFTRT相比,接受AHTRT(联合或不联合化疗)的患者局部复发率和生存率有改善趋势(分别为P = 0.06和P = 0.10)。在调整其他潜在混杂因素后,对于非鳞状细胞癌亚组患者,与AHTRT(联合或不联合化疗)相关的生存率改善具有统计学意义(P = 0.02)。比较AHTRT联合化疗与AHTRT不联合化疗时,在无全身进展生存率或总生存率方面未发现差异。
这些结果表明,与SFTRT相比,IIIA期或IIIB期非小细胞肺癌患者接受AHTRT联合或不联合化疗可能改善局部进展生存率和总生存率,尤其是对于非鳞状细胞癌患者。检测局部进展中位时间和生存率观察差异的统计效能分别约为55%和35%。因此,有必要进一步比较SFTRT与AHTRT。