Encorafenib plus cetuximab in patients with BRAFV600E-mutated metastatic colorectal cancer — Polish multicenter experience

IF 0.3 Q4 ONCOLOGY Oncology in Clinical Practice Pub Date : 2023-10-10 DOI:10.5603/ocp.96898
Marek Gełej, Patryk Zając, Maria Dąbrowska, Anna Dejws-Wątróbowska, Bogumiła Galińska, Łukasz Galus, Agnieszka Gwóźdź-Cieślik, Katarzyna Hetman, Maciej Kawecki, Mateusz Malik, Joanna Streb, Katarzyna Wierzbicka, Piotr Wiosek, Barbara Radecka
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Abstract

Introduction. The BRAF mutation occurs in 8–12% of patients with colorectal cancer. This is associated with unfavorable prognosis — in metastatic disease, median survival does not exceed one year. Molecularly targeted treatment — encorafenib with cetuximab — is the standard of care in cases of chemotherapy failure. Material and methods. Medical data of 18 patients treated with encorafenib and cetuximab in 2021–2023 in 10 oncology centers in Poland were assessed. We analyzed clinical, pathomorphological, and molecular factors, as well as the effectiveness and safety of treatment. Results. The median age in the group was 63 years. Patients with metastases limited to one location predominated (78%). Treatment with encorafenib and cetuximab was used not only in the third (in 50% of patients) or fourth (in 28%) lines of treatment but also in the second (in 22%). The objective response rate was 29.4%, and the disease control rate was 76.4%. Due to the short follow-up period, median progression-free survival was not reached. Four patients (22%) had a response lasting over 12 months. Conclusions. This study confirmed the efficacy and safety of targeted treatment with encorafenib and cetuximab in patients with metastatic colorectal cancer with the BRAF V600E mutation.
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恩科非尼加西妥昔单抗治疗brafv600e突变的转移性结直肠癌-波兰多中心经验
介绍。BRAF突变发生在8-12%的结直肠癌患者中。这与不良预后有关——在转移性疾病中,中位生存期不超过一年。分子靶向治疗——恩科非尼联合西妥昔单抗——是化疗失败病例的标准治疗方案。材料和方法。对波兰10个肿瘤中心2021-2023年接受恩科非尼和西妥昔单抗治疗的18例患者的医疗数据进行评估。我们分析了临床、病理形态学和分子因素,以及治疗的有效性和安全性。结果。研究对象的中位年龄为63岁。局限于一个部位转移的患者占多数(78%)。用encorafenib和西妥昔单抗治疗不仅用于第三(50%的患者)或第四(28%的患者)治疗,而且用于第二(22%)治疗。客观有效率为29.4%,疾病控制率为76.4%。由于随访时间短,中位无进展生存期未达到。4例患者(22%)的缓解持续时间超过12个月。结论。本研究证实了恩科非尼联合西妥昔单抗靶向治疗BRAF V600E突变转移性结直肠癌患者的有效性和安全性。
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来源期刊
CiteScore
0.90
自引率
20.00%
发文量
46
审稿时长
15 weeks
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