Sato Hiroki, Tsukahara Kiyoaki, Okamoto Isaku, Katsube Yasuaki, Shimizu Akira, Kondo Takahito, Hanyu Kenji, Fushimi Chihiro, Okada Takuro, Miura Kouki
a Department of Otorhinolaryngology, Head and Neck Surgery , Tokyo Medical University , Tokyo , Japan.
b Department of Otorhinolaryngology, Head and Neck Surgery , Tokyo Medical University Hachioji Medical Center , Tokyo , Japan.
Acta Otolaryngol. 2019 Feb;139(2):201-205. doi: 10.1080/00016489.2018.1551623. Epub 2019 Feb 22.
Combination therapy consisting of a platinum agent, 5-fluorouracil and cetuximab (EXTREME regimen) is recommended for recurrent or metastatic squamous cell carcinoma of the head and neck (R/M-SCCHN). However, it is advisable to use platinum-free regimens as first-line therapy in patients resistant to platinum agents. There has been no report comparing EXTREME regimen outcomes between platinum-resistant and platinum-sensitive patients.
We conducted this study to examine the outcomes of the EXTREME regimen as first-line therapy in patients with R/M-SCCHN and a history of platinum agent use and assess whether the EXTREME regimen outcomes differ between platinum-resistant and platinum-sensitive patients.
The study included 32 patients with R/M-SCCHN who received the EXTREME regimen as first-line therapy. Patients with recurrence or metastasis within 6 months after cisplatin administration were considered platinum-resistant and those with no recurrence or metastasis within 6 months were considered platinum-sensitive.
17 patients were platinum-resistant and 15 patients were platinum-sensitive. The median survival durations were 10.6 and 19.9 months in the platinum-resistant and platinum-sensitive patients, respectively, and the prognosis was significantly better in the platinum-sensitive patients (p = .02).
Our findings suggest that the EXTREME regimen is useful as first-line therapy for R/M-SCCHN in platinum-sensitive patients.
对于复发或转移性头颈部鳞状细胞癌(R/M-SCCHN),推荐使用由铂类药物、5-氟尿嘧啶和西妥昔单抗组成的联合疗法(EXTREME方案)。然而,对于铂类药物耐药的患者,建议使用不含铂类的方案作为一线治疗。目前尚无关于铂类耐药和铂类敏感患者EXTREME方案疗效比较的报道。
我们开展这项研究,以检验EXTREME方案作为一线治疗用于有铂类药物使用史的R/M-SCCHN患者的疗效,并评估铂类耐药和铂类敏感患者的EXTREME方案疗效是否存在差异。
该研究纳入了32例接受EXTREME方案作为一线治疗的R/M-SCCHN患者。顺铂给药后6个月内出现复发或转移的患者被视为铂类耐药,6个月内未出现复发或转移的患者被视为铂类敏感。
17例患者铂类耐药,15例患者铂类敏感。铂类耐药和铂类敏感患者的中位生存期分别为10.6个月和19.9个月,铂类敏感患者的预后明显更好(p = 0.02)。
我们的研究结果表明,EXTREME方案作为铂类敏感的R/M-SCCHN患者的一线治疗是有效的。