Ebinç Senar, Oruç Zeynep, Urakçi Zuhat, Kalkan Ziya, Kaplan Muhammet Ali, Küçüköner Mehmet, Işikdoğan Abdurrahman
Department of Medical Oncology, Dicle University Faculty of Medicine, Diyarbakır, Turkey.
Eurasian J Med. 2022 Oct;54(3):229-234. doi: 10.5152/eurasianjmed.2022.21162.
Regorafenib is a multikinase inhibitor, the effectiveness of which was demonstrated in metastatic colorectal cancer. This study aimed to investigate the factors that could predict the effectiveness of regorafenib.
This study retrospectively reviewed the clinical characteristics, tumor characteristics, and previous therapies in 62 patients who presented to our center between 2016 and 2020 and used regorafenib for metastatic colorectal cancer. The effects of the investigated variables on the response obtained with regorafenib use were evaluated.
This study included a total of 62 patients diagnosed with metastatic colorectal cancer, of whom 30 (48.4%) were males and 32 (51.6%) were females. Patients' median age at diagnosis was 49 years (18- 68). Regorafenib therapy yielded a disease control rate of 64% [complete response=0, partial response= 14 (28%), and stable disease=18 (36%)]. Objective response was obtained in 28% of patients [complete response=0 and partial response=14 (28%)]. Progression-free survival was 4 months. The evaluation of the effects of patients' age, sex, performance status, previous treatments, metastatic sites, and RAS mutation status on the disease control rate and progression-free survival did not determine any positive or negative effects on progression-free survival. However, left-sided tumors had a positive effect on disease control rate (69.8% vs. 28.6%, P=.029). and previous use of cetuximab had a negative effect on disease control rate [76.5% vs. 37.5% (P=.007)].
In our study, tumor localization and previous cetuximab use were found to be correlated with the disease control rate in patients on regorafenib. However, the need for novel biomarkers that will predict the effectiveness of regorafenib in metastatic colorectal cancer treatment persists.
瑞戈非尼是一种多激酶抑制剂,其有效性已在转移性结直肠癌中得到证实。本研究旨在探讨可预测瑞戈非尼有效性的因素。
本研究回顾性分析了2016年至2020年间在本中心就诊并使用瑞戈非尼治疗转移性结直肠癌的62例患者的临床特征、肿瘤特征及既往治疗情况。评估了所研究变量对使用瑞戈非尼获得的反应的影响。
本研究共纳入62例诊断为转移性结直肠癌的患者,其中男性30例(48.4%),女性32例(51.6%)。患者诊断时的中位年龄为49岁(18 - 68岁)。瑞戈非尼治疗的疾病控制率为64%[完全缓解=0,部分缓解=14例(28%),疾病稳定=18例(36%)]。28%的患者获得客观缓解[完全缓解=0,部分缓解=14例(28%)]。无进展生存期为4个月。评估患者年龄、性别、体能状态、既往治疗、转移部位和RAS突变状态对疾病控制率和无进展生存期的影响,未发现对无进展生存期有任何正面或负面影响。然而,左侧肿瘤对疾病控制率有正面影响(69.8%对28.6%,P = 0.029),既往使用西妥昔单抗对疾病控制率有负面影响[76.5%对37.5%(P = 0.007)]。
在我们的研究中,发现肿瘤定位和既往西妥昔单抗使用情况与接受瑞戈非尼治疗患者的疾病控制率相关。然而,仍然需要新的生物标志物来预测瑞戈非尼在转移性结直肠癌治疗中的有效性。