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首页> 外文期刊>Journal of Clinical Oncology >Hyperfractionated radiation therapy with or without concurrent low-dose daily cisplatin in locally advanced squamous cell carcinoma of the head and neck: a prospective randomized trial.
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Hyperfractionated radiation therapy with or without concurrent low-dose daily cisplatin in locally advanced squamous cell carcinoma of the head and neck: a prospective randomized trial.

机译:在头颈部局部晚期鳞状细胞癌中有或没有并发低剂量每日顺铂的超分割放射疗法:一项前瞻性随机试验。

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PURPOSE: To investigate whether the addition of cisplatin (CDDP) to hyperfractionation (Hfx) radiation therapy (RT) offers an advantage over the same Hfx RT given alone in locally advanced (stages III and IV) squamous cell carcinoma of the head and neck. PATIENTS AND METHODS: One hundred thirty patients were randomized to receive either Hfx RT alone to a tumor dose of 77 Gy in 70 fractions in 35 treatment days over 7 weeks (group I, n = 65) or the same Hfx RT and concurrent low-dose (6 mg/m(2)) daily CDDP (group II, n = 65). RESULTS: Hfx RT/chemotherapy offered significantly higher survival rates than Hfx RT alone (68% v 49% at 2 years and 46% v 25% at 5 years; P =.0075). It also offered higher progression-free survival (46% v 25% at 5 years; P =.0068), higher locoregional progression-free survival (LRPFS) (50% v 36% at 5 years; P =.041), and higher distant metastasis-free survival (DMFS) (86% v 57% at 5 years; P =.0013). However, there was no difference between the two treatment groups in the incidence of either acute or late high-grade RT-induced toxicity. Hematologic high-grade toxicity was more frequent in group II patients. CONCLUSION: As compared with Hfx RT alone, Hfx RT and concurrent low-dose daily CDDP offered a survival advantage, as well as improved LRPFS and DMFS.
机译:目的:研究在超局部分割(Hfx)放射治疗(RT)中添加顺铂(CDDP)是否比在局部晚期(III和IV期)头颈部鳞状细胞癌中单独给予的相同Hfx RT有优势。患者与方法:一百零三名患者被随机分配接受Hfx RT治疗,在7周内的35个治疗日内以70个分数(77组)接受77 Gy的肿瘤剂量(I组,n = 65),或采用相同的Hfx RT并发低剂量每日CDDP剂量(6 mg / m(2))(II组,n = 65)。结果:Hfx RT /化学疗法比单独使用Hfx RT可以提供更高的生存率(2年时68%对49%,5年时46%对25%; P = .0075)。它还提供了更高的无进展生存期(5年时46%vs 25%; P = .0068),更高的局部区域无进展生存期(LRPFS)(5年时50%vs 36%; P = .041),以及更高的远处无转移生存率(DMFS)(5年时为86%对57%; P = .0013)。但是,在两个治疗组之间,急性或晚期高放疗所致毒性的发生率没有差异。 II组患者血液学高度毒性反应更为频繁。结论:与单独的Hfx RT相比,Hfx RT和并发的低剂量每日CDDP具有生存优势,并改善了LRPFS和DMFS。

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