Guedes Alexandra, Silva Sandra, Custódio Sandra, Capela Andreia
Department of Medical Oncology, Centro Hospitalar Gaia/Espinho, Vila Nova de Gaia 4434-502, Portugal.
World J Clin Oncol. 2024 Sep 24;15(9):1232-1238. doi: 10.5306/wjco.v15.i9.1232.
Metastatic colorectal cancer (mCRC) treatment has been evolving and increasingly driven by tumor biology and gene expression analysis. Rechallenge with epidermal growth factor receptor (EGFR) inhibitors (anti-EGFR) represents a promising strategy for patients with RAS wild-type (RAS-wt) mCRC and circulating tumor DNA has emerged as a potential selection strategy. Herein, we report the case of a RAS-wt mCRC patient who had a successful response to cetuximab rechallenge.
Our patient was diagnosed with stage IV RAS-wt, microsatellite-stable rectosigmoid junction adenocarcinoma. He was started on first-line treatment with FOLFIRI and cetuximab and achieved partial response, allowing for a left hepatectomy (R0), followed by post-operative chemotherapy and an anterior resection; progression-free survival (PFS) of 16 months was obtained. Due to hepatic and nodal relapse, second-line treatment with FOLFOX and bevacizumab was started with partial response; metastasectomy was performed (R0), achieving a PFS of 11 months. After a 15 months anti-EGFR-free interval, FOLFIRI and cetuximab were reintroduced upon disease progression, again with partial response and a PFS of 16 months. Following extensive hepatic relapse, cetuximab was reintroduced and a marked clinical and analytical improvement was seen, after only one cycle. RAS-wt status was confirmed on circulating tumor DNA. The patient's overall survival exceeded 5 years.
Our case provides real-world data to support cetuximab rechallenge in later lines of RAS-wt mCRC treatment.
转移性结直肠癌(mCRC)的治疗一直在不断发展,越来越受到肿瘤生物学和基因表达分析的推动。对表皮生长因子受体(EGFR)抑制剂(抗EGFR)进行再挑战是RAS野生型(RAS-wt)mCRC患者的一种有前景的策略,循环肿瘤DNA已成为一种潜在的选择策略。在此,我们报告一例RAS-wt mCRC患者再次使用西妥昔单抗治疗取得成功的病例。
我们的患者被诊断为IV期RAS-wt、微卫星稳定的直肠乙状结肠交界处腺癌。他开始接受FOLFIRI和西妥昔单抗一线治疗并取得部分缓解,随后进行了左肝切除术(R0),接着是术后化疗和前切除术;无进展生存期(PFS)为16个月。由于肝脏和淋巴结复发,开始使用FOLFOX和贝伐单抗进行二线治疗并取得部分缓解;进行了转移灶切除术(R0),PFS为11个月。在15个月未使用抗EGFR治疗的间隔期后,疾病进展时再次引入FOLFIRI和西妥昔单抗,再次取得部分缓解,PFS为16个月。在广泛肝脏复发后,再次引入西妥昔单抗,仅一个周期后就出现了显著的临床和分析改善。循环肿瘤DNA证实为RAS-wt状态。患者的总生存期超过5年。
我们的病例提供了真实世界的数据,支持在RAS-wt mCRC治疗的后续方案中再次使用西妥昔单抗。