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多西他赛、顺铂和 5-氟尿嘧啶诱导化疗联合西妥昔单抗放疗治疗局部晚期头颈部鳞状细胞癌。

Induction chemotherapy with docetaxel, cisplatin and 5-fluorouracil followed by radiotherapy with cetuximab for locally advanced squamous cell carcinoma of the head and neck.

机构信息

Medical Dept. Int. Med. 3, Hematology and Oncology, Hanusch-Krankenhaus, Vienna, Austria.

出版信息

Eur J Cancer. 2013 Jan;49(2):352-9. doi: 10.1016/j.ejca.2012.08.004. Epub 2012 Sep 14.

DOI:10.1016/j.ejca.2012.08.004
PMID:22981499
Abstract

PURPOSE

To determine the efficacy and feasibility of induction chemotherapy (ICT) with docetaxel, cisplatin and 5-fluorouracil followed by radiotherapy and cetuximab (C) in patients with locally advanced head and neck cancer.

PATIENTS AND METHODS

Forty-nine previously untreated patients with local advanced stage III and IV squamous cell carcinoma of the head and neck (SCCHN) received three courses of ICT consisting of docetaxel 75mg/m(2) day 1, cisplatin 75mg/m(2) day 1 and infusional 5-fluorouracil 750mg/m(2)/day on days 1-5 followed by radiotherapy plus C at 250mg/m(2)/week (after an initial loading dose of 400mg/m(2)).

RESULTS

After completion of ICT 44 of 49 patients received radiotherapy plus C. Three months after therapy completion tumour response was observed in 33 patients and after two years, 25 patients were in complete remission (CR). The most common grade 4 toxicity during the whole treatment period was dermatitis (30%), followed by mucositis (27%) and neutropenia (17%) without fever. One toxic related death was observed during ICT. Two-year progression-free survival (PFS) rate was 59% and two-year overall survival (OS) rate was 63%, respectively.

CONCLUSION

Concurrent radiotherapy plus C after three courses of ICT was feasible and was associated with promising CR, PFS and OS rates. Further optimisation of dose and sequence is warranted.

摘要

目的

评估多西他赛、顺铂和氟尿嘧啶诱导化疗(ICT)联合放疗及西妥昔单抗(C)在局部晚期头颈部鳞癌患者中的疗效和可行性。

方法

49 例未经治疗的局部晚期 III 期和 IV 期头颈部鳞状细胞癌(SCCHN)患者接受了 3 个周期的 ICT,方案为多西他赛 75mg/m²,第 1 天;顺铂 75mg/m²,第 1 天;持续输注氟尿嘧啶 750mg/m²/天,第 1-5 天,然后联合放疗及每周 250mg/m²的 C(初始剂量 400mg/m²)。

结果

ICT 完成后,49 例患者中有 44 例接受了放疗加 C。治疗结束后 3 个月,33 例患者肿瘤有反应,2 年后 25 例患者完全缓解(CR)。整个治疗期间最常见的 4 级毒性是皮炎(30%),其次是黏膜炎(27%)和中性粒细胞减少(17%),但无发热。在 ICT 期间观察到 1 例与毒性相关的死亡。2 年无进展生存率(PFS)为 59%,2 年总生存率(OS)为 63%。

结论

3 个周期 ICT 后联合放疗及 C 是可行的,并与有希望的 CR、PFS 和 OS 率相关。需要进一步优化剂量和顺序。

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