Nakajima Hiromichi, Fukuoka Shota, Masuishi Toshiki, Takashima Atsuo, Kumekawa Yosuke, Kajiwara Takeshi, Yamazaki Kentaro, Negoro Yuji, Komoda Masato, Makiyama Akitaka, Denda Tadamichi, Hatachi Yukimasa, Suto Takeshi, Sugimoto Naotoshi, Enomoto Masanobu, Ishikawa Toshiaki, Kashiwada Tomomi, Ando Koji, Yuki Satoshi, Okuyama Hiroyuki, Kusaba Hitoshi, Sakai Daisuke, Okamoto Koichi, Tamura Takao, Yamashita Kimihiro, Gosho Masahiko, Moriwaki Toshikazu
Department of Gastrointestinal Oncology, National Cancer Center Hospital East, Chiba, Japan.
Division of Cancer Immunology, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Chiba, Japan.
Front Oncol. 2021 Jun 15;11:688709. doi: 10.3389/fonc.2021.688709. eCollection 2021.
Primary tumor location (PTL) is an important prognostic and predictive factor in the first-line treatment of metastatic colorectal cancer (mCRC). Although regorafenib (REG) and trifluridine/tipiracil (FTD/TPI) have been introduced recently, the clinical impact of PTL in these treatments is not well understood.
We retrospectively evaluated patients with mCRC who were registered in a multicenter observational study (the REGOTAS study). The main inclusion criteria were Eastern Cooperative Oncology Group performance status (ECOG PS) of 0-2, refractory or intolerant to fluoropyrimidines, oxaliplatin, irinotecan, angiogenesis inhibitors, anti-epidermal growth factor receptor therapy (if RAS wild-type), and no prior use of REG and FTD/TPI. The impact of PTL on overall survival (OS) was evaluated using Cox proportional hazard models based on baseline characteristics.
A total of 550 patients (223 patients in the REG group and 327 patients in the FTD/TPI group) were included in this study, with 122 patients with right-sided tumors and 428 patients with left-sided tumors. Although the right-sided patients had significantly shorter OS compared with the left-sided patients by univariate analysis ( = 0.041), a multivariate analysis revealed that PTL was not an independent prognostic factor (hazard ratio, 0.95; = 0.64). In a subgroup analysis, the OS was comparable between the REG and FTD/TPI groups regardless of PTL ( for interactions = 0.60).
In the present study, PTL is not a prognostic and predictive factor in patients with mCRC under later-line REG or FTD/TPI therapy.
原发肿瘤位置(PTL)是转移性结直肠癌(mCRC)一线治疗中一个重要的预后和预测因素。尽管瑞戈非尼(REG)和曲氟尿苷/替匹嘧啶(FTD/TPI)最近已被应用,但PTL在这些治疗中的临床影响尚不清楚。
我们回顾性评估了参加一项多中心观察性研究(REGOTAS研究)的mCRC患者。主要纳入标准为东部肿瘤协作组体能状态(ECOG PS)为0 - 2,对氟嘧啶、奥沙利铂、伊立替康、血管生成抑制剂、抗表皮生长因子受体治疗(如果RAS野生型)难治或不耐受,且既往未使用过REG和FTD/TPI。基于基线特征,使用Cox比例风险模型评估PTL对总生存期(OS)的影响。
本研究共纳入550例患者(REG组223例,FTD/TPI组327例),其中右侧肿瘤患者122例,左侧肿瘤患者428例。单因素分析显示,右侧患者的OS明显短于左侧患者(P = 0.041),但多因素分析显示PTL不是独立的预后因素(风险比,0.95;P = 0.64)。在亚组分析中,无论PTL如何,REG组和FTD/TPI组的OS相当(交互作用P = 0.60)。
在本研究中,PTL不是接受二线REG或FTD/TPI治疗的mCRC患者的预后和预测因素。