Colorectal cancer harboring EGFR kinase domain duplication response to EGFR tyrosine kinase inhibitors

Author:

Kondo Tomohiro12ORCID,Kikuchi Osamu1,Yamamoto Yoshihiro1,Sunami Tomohiko1,Wang Yafeng1,Fukuyama Keita3,Saito Tomoki1,Nakahara Hideto4,Minamiguchi Sachiko5,Kanai Masashi1,Sueyoshi Atsushi6,Muto Manabu1ORCID

Affiliation:

1. Department of Therapeutic Oncology, Graduate School of Medicine, Kyoto University , Kyoto , Japan

2. Japan Society for the Promotion of Science , Tokyo , Japan

3. Division of Medical Information Technology and Administration Planning, Kyoto University Hospital , Kyoto , Japan

4. Uji Tokushukai Medical Center Department of Surgery, , Uji , Japan

5. Kyoto University Hospital Department of Diagnostic Pathology, , Kyoto , Japan

6. Uji-Tokushukai Medical Center , Uji , Japan

Abstract

Abstract 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.

Publisher

Oxford University Press (OUP)

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