Chan A T C, Teo P M L, Ngan R K, Leung T W, Lau W H, Zee B, Leung S F, Cheung F Y, Yeo W, Yiu H H, Yu K H, Chiu K W, Chan D T, Mok T, Yuen K T, Mo F, Lai M, Kwan W H, Choi P, Johnson P J
Prince of Wales Hospital, Chinese University of Hong Kong, Shatin, N.T., Hong Kong.
J Clin Oncol. 2002 Apr 15;20(8):2038-44. doi: 10.1200/JCO.2002.08.149.
Nasopharyngeal carcinoma (NPC) is highly sensitive to both radiotherapy (RT) and chemotherapy. This randomized phase III trial compared concurrent cisplatin-RT (CRT) with RT alone in patients with locoregionally advanced NPC.
Patients with Ho's N2 or N3 stage or N1 stage with nodal size > or = 4 cm were randomized to receive cisplatin 40 mg/m(2) weekly up to 8 weeks concurrently with radical RT (CRT) or RT alone. The primary end point was progression-free survival (PFS).
Three hundred fifty eligible patients were randomized. Baseline patient characteristics were comparable in both arms. There were significantly more toxicities, including mucositis, myelosuppression, and weight loss in the CRT arm. There were no treatment-related deaths in the CRT arm, and one patient died during treatment in the RT-alone arm. At a median follow-up of 2.71 years, the 2-year PFS was 76% in the CRT arm and 69% in the RT-alone arm (P =.10) with a hazards ratio of 1.367 (95% confidence interval [CI], 0.93 to 2.00). The treatment effect had a significant covariate interaction with tumor stage, and a subgroup analysis demonstrated a highly significant difference in favor of the CRT arm in Ho's stage T3 (P =.0075) with a hazards ratio of 2.328 (95% CI, 1.26 to 4.28). For T3 stage, the time to first distant failure was statistically significantly different in favor of the CRT arm (P =.016).
Concurrent CRT is well tolerated in patients with advanced NPC in endemic areas. Although PFS was not significantly different between the concurrent CRT arm and the RT-alone arm in the overall comparison, PFS was significantly prolonged in patients with advanced tumor and node stages.
鼻咽癌(NPC)对放疗(RT)和化疗均高度敏感。本随机III期试验比较了局部晚期NPC患者同步顺铂放疗(CRT)与单纯放疗的疗效。
Ho分期为N2或N3期或N1期且淋巴结大小≥4 cm的患者被随机分为两组,一组在根治性放疗(CRT)期间每周接受40 mg/m²顺铂,共8周,另一组接受单纯放疗。主要终点是无进展生存期(PFS)。
350例符合条件的患者被随机分组。两组患者的基线特征具有可比性。CRT组的毒性反应明显更多,包括黏膜炎、骨髓抑制和体重减轻。CRT组无治疗相关死亡病例,单纯放疗组有1例患者在治疗期间死亡。中位随访2.71年时,CRT组的2年PFS为76%,单纯放疗组为69%(P = 0.10),风险比为1.367(95%置信区间[CI],0.93至2.00)。治疗效果与肿瘤分期有显著的协变量交互作用,亚组分析显示,在Ho分期T3患者中,CRT组有高度显著差异(P = 0.0075),风险比为2.328(95%CI,1.26至4.28)。对于T3期,首次远处转移失败时间在CRT组有统计学显著差异(P = 0.016)。
在流行地区,晚期NPC患者对同步CRT耐受性良好。尽管在总体比较中,同步CRT组与单纯放疗组的PFS无显著差异,但在肿瘤和淋巴结分期较晚的患者中,PFS显著延长。