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西妥昔单抗、顺铂与同期增量放疗联合治疗局部晚期头颈部鳞状细胞癌:一种新型联合治疗模式的II期初步研究

Concurrent cetuximab, cisplatin, and concomitant boost radiotherapy for locoregionally advanced, squamous cell head and neck cancer: a pilot phase II study of a new combined-modality paradigm.

作者信息

Pfister David G, Su Yungpo Bernard, Kraus Dennis H, Wolden Suzanne L, Lis Eric, Aliff Timothy B, Zahalsky Andrew J, Lake Simone, Needle Michael N, Shaha Ashok R, Shah Jatin P, Zelefsky Michael J

机构信息

Memorial Sloan-Kettering Cancer Center, 1275 York Ave, New York, NY 10021, USA.

出版信息

J Clin Oncol. 2006 Mar 1;24(7):1072-8. doi: 10.1200/JCO.2004.00.1792.

Abstract

PURPOSE

Cetuximab is a chimeric monoclonal antibody that targets the epidermal growth factor receptor. Cetuximab has activity in squamous cell carcinoma and enhances both chemotherapy and radiotherapy. We conducted a pilot phase II study of a new combined-modality paradigm of targeted therapy (cetuximab) with chemoradiotherapy.

PATIENTS AND METHODS

Eligible patients had stage III or IV, M0, squamous cell head and neck cancer. Treatment included concomitant boost radiotherapy (1.8 Gy/d weeks 1 to 6; boost: 1.6 Gy 4 to 6 hours later weeks 5 to 6; 70 Gy total to gross disease), cisplatin (100 mg/m2 intravenously weeks 1 and 4), and cetuximab (400 mg/m2 intravenously week 1, followed by 250 mg/m2 weeks 2 to 10).

RESULTS

Twenty-two patients were enrolled (median age, 57 years; range, 41 to 72 years; median Karnofsky status, 90%; range, 70% to 90%; oropharynx primary tumor, 59% of patients; T4, 36%; N2/3, 77%; stage IV disease, 86%). One patient did not receive study treatment because of an ineligible diagnosis. The severity of expected, acute toxicities was typical of concurrent cisplatin and radiotherapy alone. Grade 3 or 4 cetuximab-related toxicities included acne-like rash (10%) and hypersensitivity (5%). However, the study was closed for significant adverse events, including two deaths (one pneumonia and one unknown cause), one myocardial infarction, one bacteremia, and one atrial fibrillation. With a median follow-up of 52 months, the 3-year overall survival rate is 76%, the 3-year progression-free survival rate is 56%, and the 3-year locoregional control rate is 71%.

CONCLUSION

This regimen is not currently recommended outside of the clinical trial setting. Further investigation of its safety profile is needed. However, preliminary efficacy is encouraging, and further development of this targeted combined-modality paradigm is warranted.

摘要

目的

西妥昔单抗是一种靶向表皮生长因子受体的嵌合单克隆抗体。西妥昔单抗在鳞状细胞癌中具有活性,可增强化疗和放疗效果。我们开展了一项关于靶向治疗(西妥昔单抗)联合放化疗新联合模式的II期试点研究。

患者与方法

符合条件的患者患有III期或IV期、M0期鳞状细胞头颈癌。治疗包括同步推量放疗(第1至6周每天1.8 Gy;推量:第5至6周在4至6小时后给予1.6 Gy;大体肿瘤总量达70 Gy)、顺铂(第1周和第4周静脉注射100 mg/m²)以及西妥昔单抗(第1周静脉注射400 mg/m²,随后第2至10周每周250 mg/m²)。

结果

共纳入22例患者(中位年龄57岁;范围41至72岁;中位卡诺夫斯基状态90%;范围70%至90%;口咽原发性肿瘤患者占59%;T4期占36%;N2/3期占77%;IV期疾病占86%)。1例患者因诊断不符合条件未接受研究治疗。预期的急性毒性严重程度为单独同步使用顺铂和放疗时的典型情况。3级或4级与西妥昔单抗相关的毒性包括痤疮样皮疹(10%)和超敏反应(5%)。然而,该研究因严重不良事件而终止,包括2例死亡(1例肺炎和1例原因不明)、1例心肌梗死、1例菌血症和1例心房颤动。中位随访52个月时,3年总生存率为76%,3年无进展生存率为56%,3年局部区域控制率为71%。

结论

目前在临床试验环境之外不推荐使用该方案。需要进一步研究其安全性。然而,初步疗效令人鼓舞,这种靶向联合模式值得进一步开发。

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