Cicero Giuseppe, Addeo Raffaele, De Luca Rossella, Lo Re Giuseppe, Gulotta Leonardo, Marchesa Pierenrico, Gulotta Gaspare
Department of Surgical, Oncological and Oral Sciences, Section of Medical Oncology, University of Palermo, Palermo, Italy.
Oncology Unit, ASLNapoli2NORD, Frattamaggiore (Na), Italy.
Drugs Context. 2020 Sep 18;9. doi: 10.7573/dic.2020-6-3. eCollection 2020.
TAS-102 is an oral monotherapy, combining trifluridine and tipiracil hydrochloride, indicated for the treatment of pretreated metastatic colorectal cancer (mCRC). The aim of this real-life study is to evaluate the efficacy and safety of TAS-102 in heavily pretreated elderly patients with mCRC whose disease has progressed with standard therapies.
In this retrospective observational study, we enrolled 50 elderly patients >70 years of age (median age 78 years) with a diagnosis of mCRC who were previously treated or were not considered candidates for treatment with other available therapies. Patients aged >70 years with advanced colorectal cancer and with an ECOG performance status of grade 0 (=18) or grade 1 (=32) were included. Overall survival and progression-free survival were the primary endpoints, whereas objective response rate, tolerability, and quality of life were the secondary endpoints.
Treatment with TAS-102 appeared to be well tolerated and side effects were generally mild, achieving disease control and a benefit on quality of life. The median overall survival was 6.7 (95% CI 5.7-11.3) and the median progression-free survival was 2.1 months (95% CI 1.2-3.2), estimated using the Kaplan-Meier method.
TAS-102 represents a manageable and effective therapeutic opportunity and appeared to be well tolerated with generally mild side effects in elderly patients with mCRC who were heavily pretreated with standard therapies.
TAS-102是一种口服单一疗法,由曲氟尿苷和盐酸替匹嘧啶组成,用于治疗经预处理的转移性结直肠癌(mCRC)。这项真实世界研究的目的是评估TAS-102在疾病已进展且接受过标准治疗的老年mCRC患者中的疗效和安全性。
在这项回顾性观察研究中,我们纳入了50名年龄>70岁(中位年龄78岁)、诊断为mCRC且之前接受过治疗或不被认为适合接受其他可用疗法治疗的患者。纳入了年龄>70岁、患有晚期结直肠癌且东部肿瘤协作组(ECOG)体能状态为0级(=18例)或1级(=32例)的患者。总生存期和无进展生存期是主要终点,而客观缓解率、耐受性和生活质量是次要终点。
TAS-102治疗耐受性良好,副作用一般较轻,实现了疾病控制并改善了生活质量。使用Kaplan-Meier方法估计,中位总生存期为6.7个月(95%CI 5.7-11.3),中位无进展生存期为2.1个月(95%CI 1.2-3.2)。
TAS-102是一种可管理且有效的治疗选择,对于接受过标准疗法充分预处理的老年mCRC患者,耐受性良好,副作用一般较轻。