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局部晚期头颈部鳞状细胞癌同步放化疗后辅助化疗(奈达铂/替加氟尿嘧啶)

[Adjuvant chemotherapy (nedaplatin/UFT) after concurrent chemoradiotherapy for locally advanced head and neck squamous cell carcinoma].

作者信息

Kubota Akira, Furukawa Madoka, Komatsu Masanori, Hanamura Hideaki, Sugiyama Masato

机构信息

Department of Head and Neck Surgery Kanagawa Cancer Center, Yokohama.

出版信息

Nihon Jibiinkoka Gakkai Kaiho. 2006 Mar 20;109(3):149-56. doi: 10.3950/jibiinkoka.109.149.

Abstract

To evaluate the efficacy of adjuvant chemotherapy after concurrent chemoradiotherapy, 41 previously untreated patients with locally advanced and resectable head and neck squamous cancer were enrolled in a study to compare adjuvant chemotherapy (Nedaplatin/UFT) after concurrent chemoradiotherapy (CDDP/5-FU) and concurrent chemoradiation alone. Nine of the patients had stage III tumors and 32 had stage IV tumors. The primary tumor site was the hypopharynx in 14 patients, the larynx in 12 patients, the oral cavity in 9 patients, and the oropharynx in 6 patients. Treatment consisted of 6 courses of Nedaplatin (80 mg/m2) repeated at 4-week intervals and one year of the oral administration of UFTE (400 mg/day) after concurrent chemoradiotherapy at an outpatient clinic. Toxicities included leukopenia (grade 3, 15.4%) and thrombocytopenia (grade 3, 7.7%). One death from a gastric ulcer occurred. The median overall survival time was 30.1 months (5.5-50.1 months) for the adjuvant chemotherapy group and 21.7 months (4.0-48.8 months) for the control group. The progression-free survival period was 22.8 months (5.6-33.9 months) for the adjuvant chemotherapy group and 26.5 months (5.6-33.9 months) for the control group. The two-year overall survival rate was 73.3% for the adjuvant chemotherapy group and 55.7% for the control group. A significant difference was observed in the two-year progression-free survival rates: 66.9% for the adjuvant chemotherapy group and 27.8% for the control group (p = 0.03290). Among the patients with a partial response to concurrent chemoradiotherapy, in particular, a significant difference in the two-year progression-free survival rates was seen : 59.3% for the adjuvant chemotherapy group and 15.3% for the control group (p = 0.01102). The rate of loco-regional failure was 29.6% for the adjuvant chemotherapy group and 64.3% for the control group (p = 0.0716). Distant metastasis was not detected in either group. The rate of organ preservation was 66.7% for the adjuvant chemotherapy group and 35.7% for the control group (p = 0.1183). This adjuvant chemotherapy regimen might improve the loco-regional control rates after concurrent chemoradiotherapy.

摘要

为评估同步放化疗后辅助化疗的疗效,41例既往未接受过治疗的局部晚期且可切除的头颈部鳞状癌患者被纳入一项研究,以比较同步放化疗(顺铂/5-氟尿嘧啶)后辅助化疗(奈达铂/优福定)与单纯同步放化疗的效果。其中9例患者为Ⅲ期肿瘤,32例为Ⅳ期肿瘤。原发肿瘤部位为下咽14例、喉12例、口腔9例、口咽6例。治疗方案为每4周重复进行6个疗程的奈达铂(80mg/m²)治疗,并在门诊同步放化疗后口服优福定(400mg/天)1年。毒性反应包括白细胞减少(3级,15.4%)和血小板减少(3级,7.7%)。有1例患者死于胃溃疡。辅助化疗组的中位总生存时间为30.1个月(5.5 - 50.1个月),对照组为21.7个月(4.0 - 48.8个月)。辅助化疗组的无进展生存期为22.8个月(5.6 - 33.9个月),对照组为26.5个月(5.6 - 33.9个月)。辅助化疗组的两年总生存率为73.3%,对照组为55.7%。在两年无进展生存率方面观察到显著差异:辅助化疗组为66.9%,对照组为27.8%(p = 0.03290)。特别是在对同步放化疗有部分反应的患者中,两年无进展生存率存在显著差异:辅助化疗组为59.3%,对照组为15.3%(p = 0.01102)。辅助化疗组的局部区域失败率为29.6%,对照组为64.3%(p = 0.0716)。两组均未检测到远处转移。辅助化疗组的器官保留率为66.7%,对照组为35.7%(p = 0.1183)。这种辅助化疗方案可能会提高同步放化疗后的局部区域控制率。

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