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作 者:Ji-Lin Guan Jian-Hua Liu Qing Wang Yu-Wei Cong Yao-Xu Chen Ke-Fei Huang Meng-Li Huang Ling Huang
机构地区:[1]Department of Oncology,Guangdong Provincial People's Hospital and Guangdong Academy of Medical Sciences,Guangzhou 510655,Guangdong Province,China [2]The Medical Department,3D Medicines Inc.,Shanghai 201114,China [3]The Bioinformatic Department,3D Medicines Inc.,Shanghai 201114,China
出 处:《World Journal of Gastrointestinal Oncology》2020年第9期1065-1072,共8页世界胃肠肿瘤学杂志(英文版)(电子版)
摘 要:BACKGROUND Human epidermal growth factor receptor 2(HER2)amplification is a molecular driver for a subset of colorectal cancers(CRCs)and one of the major causes of anti-epidermal growth factor receptor(EGFR)treatment failure.Compared to dual anti-HER2 treatments,which have been shown to be effective in HER2-positive metastatic CRC patients,single-agent anti-HER2 therapy is rarely used to treat CRC.CASE SUMMARY Herein,we report a case of RAS/BRAF-wild-type metastatic CRC that was identified as HER2-positive through circulating tumor DNA(ctDNA)testing by next-generation sequencing following the failure of two lines of therapy.Subsequently,the patient was given lapatinib monotherapy that led to a partial response with a progression-free survival of 7.9 mo.Moreover,serial ctDNA detection was used to monitor the efficacy of lapatinib.The aberration of HER2 copy number disappeared when radiographic assessment revealed a partial response.However,a high level of HER2 amplification was detected again at the time of disease progression.Finally,a phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha mutation was identified at the time of tumor progression,which may explain the acquired resistance to lapatinib.CONCLUSION This is the first case report of HER2-positive RAS/BRAF wild-type metastatic CRC patient responding to lapatinib monotherapy.It highlights that ctDNA testing is an effective and feasible approach to evaluate the efficacy of anti-HER2 therapy.
关 键 词:Human epidermal growth factor receptor 2 Colorectal cancer LAPATINIB Circulating tumor DNA Case report
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