GenesisCare Radiation Oncology, Division Radiation Oncology, St. Vincent's Hospital, Melbourne, Australia; Division of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.
Biostatistical Clinical Trials Department, Peter MacCallum Cancer Centre, Melbourne, Australia.
Int J Radiat Oncol Biol Phys. 2017 Jul 15;98(4):948-954. doi: 10.1016/j.ijrobp.2017.02.088. Epub 2017 Feb 24.
To report on the outcomes of a novel treatment regimen for patients with locally advanced head and neck squamous cell carcinoma who were fit for curative treatment but not fit for cisplatin.
Single-arm phase 1/2 study of previously untreated patients with biopsy-proven SCC of the oropharynx, larynx, or hypopharynx. The primary endpoint was feasibility of the regimen, defined as the proportion of patients successfully completing treatment. Secondary endpoints were locoregional control (LRC), failure-free survival (FFS), overall survival (OS), and treatment toxicities.
Sixty patients were included in the study. Their mean age was 66 years (range, 42-87 years); 28% of patients were >70 years. The median follow-up time was 4 years. Compliance with treatment was very high: feasibility was 55/60 (91.7%, 90% CI: 83.3%-96.7%), which satisfied the predefined criteria. The 4-year LRC was 82% (95% CI: 71-94), the FFS was 72% (95% CI: 60-85), and the OS was 77% (95% CI: 66-90). The cumulative incidences of first failure of any type at 4 years were 5.2% local, 1.8% local and distant, 8.5% regional, 1.7% regional and distant, 3.5% distant, and 7.7% death (any cause). The 4-year FFS in the patients aged ≤70 years and >70 years were 71% (95% CI: 58-88) and 73% (95% CI: 54-100), respectively (log-rank P=.801). Their 4-year OS was 79% (95% CI: 66-93) and 73% (95% CI: 53-100), respectively (log-rank P=.708). Significant late treatment toxicities were very few.
This treatment regimen was feasible and safe in this patient cohort unfit for cisplatin, 28% of whom were older than 70 years. Carboplatin-based and cetuximab-based chemoradiation regimens warrant further investigation in patients with a contraindication to cisplatin.
报告一种新的治疗方案在适合根治性治疗但不适合顺铂治疗的局部晚期头颈部鳞状细胞癌患者中的结果。
单臂 1/2 期研究,纳入经活检证实的口咽、喉或下咽鳞状细胞癌的未经治疗的患者。主要终点是方案的可行性,定义为成功完成治疗的患者比例。次要终点是局部区域控制(LRC)、无失败生存(FFS)、总生存(OS)和治疗毒性。
60 例患者纳入研究。他们的平均年龄为 66 岁(范围:42-87 岁);28%的患者年龄大于 70 岁。中位随访时间为 4 年。治疗的依从性非常高:可行性为 55/60(91.7%,90%CI:83.3%-96.7%),满足了预设标准。4 年 LRC 为 82%(95%CI:71-94),FFS 为 72%(95%CI:60-85),OS 为 77%(95%CI:66-90)。4 年时任何类型首次失败的累积发生率为 5.2%局部、1.8%局部和远处、8.5%区域、1.7%区域和远处、3.5%远处和 7.7%死亡(任何原因)。≤70 岁和>70 岁患者的 4 年 FFS 分别为 71%(95%CI:58-88)和 73%(95%CI:54-100)(对数秩 P=.801)。他们的 4 年 OS 分别为 79%(95%CI:66-93)和 73%(95%CI:53-100)(对数秩 P=.708)。明显的晚期治疗毒性非常少。
在不适合顺铂的患者中,该治疗方案在这组患者中是可行和安全的,其中 28%的患者年龄大于 70 岁。对于有顺铂禁忌证的患者,卡铂和西妥昔单抗为基础的放化疗方案值得进一步研究。