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诱导 TPF 化疗后行 CRT,局部晚期不可切除头颈部癌患者采用分次顺铂给药。

Induction TPF chemotherapy followed by CRT with fractionated administration of cisplatin in patients with unresectable locally advanced head and neck cancer.

机构信息

Department of Head and Neck Medical Oncology, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba, 277-8577, Japan.

Department of Medical Oncology, Hyogo Cancer Center, Akashi, Hyogo, Japan.

出版信息

Int J Clin Oncol. 2019 Jul;24(7):789-797. doi: 10.1007/s10147-019-01418-w. Epub 2019 Feb 22.

Abstract

BACKGROUND

In treatment of locally advanced squamous cell carcinoma of the head and neck (SCCHN), the use of docetaxel, cisplatin, and 5-fluorouracil (TPF) followed by high-dose cisplatin chemoradiotherapy (CRT) carries concerns over toxicity. We evaluated the feasibility of TPF as induction chemotherapy (IC) to Japanese patients and the tolerability of CRT with fractionated administration of cisplatin after IC.

METHODS

Patients with unresectable stage III, IV SCCHN received IC followed by CRT. IC consisted of three 3-week cycles of docetaxel 70-75 mg/m on day 1, cisplatin 70-75 mg/m on day 1, and 5-fluorouracil 750 mg/m on days 1-5. Patients subsequently received IMRT concomitant with fractionated administration of cisplatin (20 mg/m) on days 1-4, repeated every 3 weeks. The primary endpoint was completion of the three cycles of IC.

RESULTS

Forty-eight patients were enrolled. The IC treatment completion rate was 85%. Grade 3-4 toxicities of TPF were neutropenia (79%) and febrile neutropenia (15%). Thirty-eight patients (79%) achieved a response after IC. Forty patients subsequently underwent CRT. Thirty-three patients (83%) completed the planned cycles of fractionated administration of cisplatin, but seven (18%) did not. Grade 3-4 toxicities during CRT were neutropenia (23%), mucositis (53%), and dysphagia (33%). With a median follow-up of 36.1 months, 3-year overall survival was 65%.

CONCLUSION

TPF IC is feasible and CRT with fractionated administration of cisplatin after IC is tolerable. IC followed by CRT appears to be a useful and safe sequential treatment. (Trial registration no. UMIN000024686).

摘要

背景

在治疗局部晚期头颈部鳞状细胞癌(SCCHN)时,使用多西紫杉醇、顺铂和 5-氟尿嘧啶(TPF)联合高剂量顺铂放化疗(CRT)存在毒性问题。我们评估了 TPF 作为诱导化疗(IC)在日本患者中的可行性,以及在 IC 后分阶段给予顺铂的 CRT 的耐受性。

方法

不可切除的 III 期、IV 期 SCCHN 患者接受 IC 后行 CRT。IC 包括三个 3 周周期,第 1 天给予多西紫杉醇 70-75mg/m2,第 1 天给予顺铂 70-75mg/m2,第 1-5 天给予 5-氟尿嘧啶 750mg/m2。随后患者接受 IMRT 联合分阶段给予顺铂(20mg/m2),每 3 周重复一次。主要终点是完成三个周期的 IC。

结果

共纳入 48 例患者。IC 治疗完成率为 85%。TPF 的 3-4 级毒性为中性粒细胞减少(79%)和发热性中性粒细胞减少(15%)。IC 后 38 例(79%)患者获得缓解。40 例患者随后接受 CRT。33 例(83%)患者完成了计划的顺铂分阶段给药周期,但 7 例(18%)未完成。CRT 期间的 3-4 级毒性为中性粒细胞减少(23%)、黏膜炎(53%)和吞咽困难(33%)。中位随访 36.1 个月后,3 年总生存率为 65%。

结论

TPF IC 是可行的,IC 后分阶段给予顺铂的 CRT 是可耐受的。IC 后行 CRT 似乎是一种有用且安全的序贯治疗方法。(试验注册号:UMIN000024686)。

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