Literature DB >> 34214965

Response to Trastuzumab and Lapatinib in a Metastatic Colorectal Cancer Harboring HER2 Amplification and HER2 S310F Mutation.

Chongkai Wang1, Marwan Fakih1.   

Abstract

Dual HER2-targeted therapy has been associated with clinical responses and prolonged progression-free survival and overall survival in RAS-wild type HER2-amplified colorectal cancer (CRC). However, no clinical benefits have been reported in patients with CRC with HER2 mutations. Activated HER2 mutations have been largely deemed resistant to trastuzumab and to dual HER2 targeting. This report describes a patient with metastatic CRC with concurrent HER2 amplification and a HER2 S310F mutation, which is an active mutation located in the extracellular dimerization domain of HER2. Treatment with trastuzumab + lapatinib resulted in an excellent response that lasted for 10 months. Upon disease progression, treatment with the antibody-drug conjugate trastuzumab-deruxtecan resulted in a short-lived response. This is the first case report of successful HER2 targeting in metastatic CRC with concurrent HER2 amplification and a HER2 S310F mutation.

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Year:  2021        PMID: 34214965     DOI: 10.6004/jnccn.2021.7023

Source DB:  PubMed          Journal:  J Natl Compr Canc Netw        ISSN: 1540-1405            Impact factor:   11.908


  2 in total

1.  m7G-Related DNA Damage Repair Genes are Potential Biomarkers for Predicting Prognosis and Immunotherapy Effectiveness in Colon Cancer Patients.

Authors:  Shuran Chen; Rui Dong; Yan Li; Ni Zheng; Guisen Peng; Fei Lu; Quanwei Qiu; Hexin Wen; Yitong Wang; Huazhang Wu; Mulin Liu
Journal:  Front Genet       Date:  2022-06-09       Impact factor: 4.772

2.  Tumor-infiltrating immune cells based TMEscore and related gene signature is associated with the survival of CRC patients and response to fluoropyrimidine-based chemotherapy.

Authors:  Xian-Wen Guo; Si-Qi Li; Rong-E Lei; Zhen Ding; Bang-Li Hu; Rong Lin
Journal:  Front Oncol       Date:  2022-08-30       Impact factor: 5.738

  2 in total

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