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一项诱导性纳武利尤单抗紫杉醇和顺铂与氟尿嘧啶联合治疗局部晚期头颈部鳞状细胞癌,随后同步放化疗的 2 期临床试验。

A phase 2 trial of induction nab-paclitaxel and cetuximab given with cisplatin and 5-fluorouracil followed by concurrent cisplatin and radiation for locally advanced squamous cell carcinoma of the head and neck.

机构信息

Division of Medical Oncology, Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.

出版信息

Cancer. 2013 Feb 15;119(4):766-73. doi: 10.1002/cncr.27741. Epub 2012 Sep 18.

Abstract

BACKGROUND

Complete response (CR) at the primary tumor site as assessed by clinical examination following induction chemotherapy with PF (cisplatin and 5-fluorouracil [5-FU]) is a favorable predictive factor for overall survival and disease control in patients with locally advanced squamous cell carcinoma of the head and neck. In most series, the rate of CR at the primary site after induction PF was 20% to 30%. This study evaluated the efficacy and feasibility of induction nab-paclitaxel and cetuximab given with PF (ACPF) followed by definitive chemoradiation (CRT) in a phase 2 trial.

METHODS

Patients with squamous cell carcinoma of the head and neck were treated with ACPF (nab-paclitaxel 100 mg/m(2) /week; cetuximab 250 mg/m(2) /week; cisplatin 75 mg/m(2) on day 1; 5-FU 750 mg/m(2) /day on days 1 through 3) every 21 days for 3 cycles followed by CRT (cisplatin 100 mg/m(2) on days 1, 22, and 43 of radiation therapy [RT]). CR at the primary tumor site after 2 cycles of ACPF was the primary endpoint.

RESULTS

Thirty patients were enrolled, of which 22 (73%) had large (T3/T4) primary tumors. The CR rate at the primary tumor site after 2 cycles of ACPF was 53% and the overall response rate was 100%. Twenty-nine (96%) patients completed 3 cycles of ACPF, 26 (90%) completed definitive RT per protocol, and 22 of the 27 evaluable patients (81%) received > 2 of the 3 planned doses of cisplatin with RT. The estimated 2-year overall and progression-free survival rates were 84% and 65%, respectively.

CONCLUSIONS

Induction ACPF resulted in a high CR rate (53%) at the primary tumor site even in large tumors and did not adversely affect delivery of definitive CRT. Further investigation of ACPF is warranted.

摘要

背景

经诱导化疗联合 PF(顺铂和 5-氟尿嘧啶[5-FU])治疗后,原发肿瘤部位完全缓解(CR)是局部晚期头颈部鳞状细胞癌患者总生存和疾病控制的有利预测因素。在大多数研究中,诱导化疗后原发部位 CR 率为 20%至 30%。本研究在一项 2 期试验中评估了诱导纳武单抗紫杉醇和西妥昔单抗联合 PF(ACPF)后行确定性放化疗(CRT)的疗效和可行性。

方法

头颈部鳞状细胞癌患者接受 ACPF(纳武单抗紫杉醇 100mg/m²/周;西妥昔单抗 250mg/m²/周;顺铂 75mg/m²第 1 天;5-FU 750mg/m²/天第 1 至 3 天)治疗,每 21 天为 1 个周期,共 3 个周期,随后行 CRT(顺铂 100mg/m²,在放疗第 1、22 和 43 天)。ACPF 治疗 2 个周期后原发肿瘤部位 CR 是主要终点。

结果

共入组 30 例患者,其中 22 例(73%)有大(T3/T4)原发肿瘤。ACPF 治疗 2 个周期后原发肿瘤部位 CR 率为 53%,总缓解率为 100%。29 例(96%)患者完成 3 个周期的 ACPF 治疗,26 例(90%)患者按方案完成了确定性 RT,27 例可评估患者中有 22 例(81%)在接受 RT 时接受了 > 3 个计划剂量的顺铂。估计 2 年总生存率和无进展生存率分别为 84%和 65%。

结论

诱导 ACPF 治疗即使在大肿瘤中也能获得很高的原发肿瘤部位 CR 率(53%),且不会对确定性 CRT 的实施产生不利影响。进一步研究 ACPF 是必要的。

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