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BRAF 突变型转移性结直肠癌患者的治疗结果:一项波兰回顾性队列研究。

Treatment outcomes of patients with BRAF-mutated metastatic colorectal cancer: a Polish retrospective cohort study.

作者信息

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

机构信息

Department of Oncology, Military Institute of Medicine, National Research Institute, Warsaw, Poland.

Department of Pathomorphology, Medical University of Gdańsk, Gdańsk, Poland.

出版信息

Contemp Oncol (Pozn). 2024;28(4):297-303. doi: 10.5114/wo.2024.146953. Epub 2025 Jan 15.

Abstract

INTRODUCTION

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.

MATERIAL AND METHODS

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.

RESULTS

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).

CONCLUSIONS

This study highlights the unmet need for effective treatment strategies for patients with BRAF-mutated mCRC in Poland.

摘要

引言

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。

材料与方法

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。

结果

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)。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3276/11809569/b3dbb89e35a1/WO-28-55530-g001.jpg

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