Kondo Tomohiro, Kikuchi Osamu, Yamamoto Yoshihiro, Sunami Tomohiko, Wang Yafeng, Fukuyama Keita, Saito Tomoki, Nakahara Hideto, Minamiguchi Sachiko, Kanai Masashi, Sueyoshi Atsushi, Muto Manabu
Department of Therapeutic Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Japan Society for the Promotion of Science, Tokyo, Japan.
Oncologist. 2025 Feb 6;30(2). doi: 10.1093/oncolo/oyae113.
Epidermal growth factor receptor kinase domain duplication (EGFR-KDD) is a rare, recurrent oncogenic variant that constitutively activates EGFR in non-small-cell lung cancer. Herein, we report the case of a 70-year-old man with resectable colorectal adenocarcinoma who underwent surgery followed by adjuvant therapy. He relapsed with multiple liver metastases and received standard chemotherapy until his disease became refractory. Comprehensive genomic profiling of his postoperative colorectal cancer tissue revealed EGFR-KDD. He was treated with an EGFR tyrosine kinase inhibitor (TKI), afatinib and achieved a partial response (- 55%) after 8 weeks; however, he developed massive malignant ascites after 13 weeks. Osimertinib, another EGFR-TKI, controlled his tumors for 9 months. Patient-derived cancer organoids from his malignant ascites confirmed sensitivity to EGFR-TKIs. The findings suggest that EGFR-TKIs can be a potential treatment option for this molecular subgroup.
表皮生长因子受体激酶结构域重复(EGFR-KDD)是一种罕见的、复发性致癌变异,可在非小细胞肺癌中持续激活EGFR。在此,我们报告一例70岁可切除结肠腺癌男性患者的病例,该患者接受了手术及辅助治疗。他出现多发肝转移复发,接受标准化疗直至疾病变得难治。对其术后结直肠癌组织进行的综合基因组分析显示存在EGFR-KDD。他接受了表皮生长因子受体酪氨酸激酶抑制剂(TKI)阿法替尼治疗,8周后获得部分缓解(-55%);然而,13周后他出现了大量恶性腹水。另一种表皮生长因子受体酪氨酸激酶抑制剂奥希替尼控制其肿瘤达9个月。从他的恶性腹水中提取的患者来源的癌症类器官证实对表皮生长因子受体酪氨酸激酶抑制剂敏感。这些发现表明,表皮生长因子受体酪氨酸激酶抑制剂可能是该分子亚组的一种潜在治疗选择。