Żok Jolanta, Bieńkowski Michał, Radecka Barbara, Kuchar Agata, Borowiec Szymon, Streb Joanna, Jurczyk Michał, Jakieła-Drąg Anna, Gełej Marek, Zając Patryk, Ploch-Glapińska Małgorzata, Duchnowska Renata
Department of Oncology, Military Institute of Medicine, National Research Institute, Warsaw, Poland.
Department of Pathomorphology, Medical University of Gdańsk, Gdańsk, Poland.
Contemp Oncol (Pozn). 2024;28(4):297-303. doi: 10.5114/wo.2024.146953. Epub 2025 Jan 15.
The BRAF mutation is found in 6-11% of metastatic colo-rectal cancer (mCRC) patients. According to international guidelines for BRAF-mutated mCRC, the triplet chemotherapy FOLFOXIRI (folinic acid, 5-fluorouracil, oxaliplatin, irinotecan) or double chemotherapy with or without bevacizumab, and encorafenib plus cetuximab should be considered in the first- and second-line settings. We aimed to evaluate clinical practices in BRAF-mutated mCRC patients treated at five Polish oncology centers.
We retrospectively analyzed the data of BRAF- mutated mCRC patients treated between 2011 and 2023. Before starting the first-line treatment, all patients were tested for BRAF and RAS mutations.
One hundred twenty-six patients (median age: 68 years; 55% female, 45% male) from five oncology centers were included. The majority of patients (69, 55%) had a right-sided primary tumor. The first line of chemotherapy was received by 100 patients (79.4%). The majority received doublet chemotherapy: FOLFOX (folinic acid, 5-fluorouracil, oxaliplatin), FOLFIRI (folinic acid, 5-fluorouracil, irinotecan), XELOX (capecitabine, oxaliplatin), and FOLFIRI with bevacizumab: 30 (30%), 47 (47%), 5 (5%), and 3 (3%). Only three patients received FOLFOXIRI; one patient received bevacizumab. The median duration of first-line treatment was 5.26 months (95% CI: 0.03-18.9). Subsequently, 40%, 16%, 5%, and 1% of patients received second, third, fourth, and fifth-line therapy, retrospectively. During the median follow-up of 38.5 months, 96 (79.3%) patients died. The median overall survival from the time of mCRC diagnosis was 13.7 months (95% CI: 11.3-17.6).
This study highlights the unmet need for effective treatment strategies for patients with BRAF-mutated mCRC in Poland.
在6%-11%的转移性结直肠癌(mCRC)患者中发现了BRAF突变。根据BRAF突变型mCRC的国际指南,一线和二线治疗应考虑三联化疗FOLFOXIRI(亚叶酸、5-氟尿嘧啶、奥沙利铂、伊立替康)或联合或不联合贝伐单抗的双联化疗,以及恩考芬尼联合西妥昔单抗。我们旨在评估在波兰五个肿瘤中心接受治疗的BRAF突变型mCRC患者的临床实践。
我们回顾性分析了2011年至2023年间接受治疗的BRAF突变型mCRC患者的数据。在开始一线治疗前,所有患者均接受了BRAF和RAS突变检测。
纳入了来自五个肿瘤中心的126例患者(中位年龄:68岁;55%为女性,45%为男性)。大多数患者(69例,55%)的原发肿瘤位于右侧。100例患者(79.4%)接受了一线化疗。大多数患者接受双联化疗:FOLFOX(亚叶酸、5-氟尿嘧啶、奥沙利铂)、FOLFIRI(亚叶酸、5-氟尿嘧啶、伊立替康)、XELOX(卡培他滨、奥沙利铂)以及联合贝伐单抗的FOLFIRI:分别为30例(30%)、47例(47%)、5例(5%)和3例(3%)。仅3例患者接受了FOLFOXIRI治疗;1例患者接受了贝伐单抗治疗。一线治疗的中位持续时间为5.26个月(95%CI:0.03-18.9)。随后,回顾性分析显示,40%、16%、5%和1%的患者接受了二线、三线、四线和五线治疗。在中位随访38.5个月期间,96例(79.3%)患者死亡。从mCRC诊断时起的中位总生存期为13.7个月(95%CI:11.3-17.6)。
本研究突出了波兰BRAF突变型mCRC患者对有效治疗策略的未满足需求。