151. Fibroblast growth factor receptor 1 gene amplification is associated with poor survival in patients with resected esophageal squamous cell carcinoma
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Joo Hang Kim, Hye Ryun Kim, Jin Hur, Yong Wha Moon, Da Hyun Jung, Hyunsoo Chung, Sung Kwan Shin, Young Mog Shim, Yoon La Choi, Susan S. Jewell, Seung Eun Lee, Chang Geol Lee, Byoung Chul Cho, Yong Chan Lee, Dae Joon Kim, Sang Kil Lee, Yoon Sung Bae, Hyo Song Kim, Hyunki Kim, and Jun Chul Park
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Adult ,Male ,Oncology ,Prognostic factor ,medicine.medical_specialty ,Pathology ,Esophageal Neoplasms ,gene amplification ,Kaplan-Meier Estimate ,Esophageal squamous cell carcinoma ,Disease-Free Survival ,Risk Factors ,Internal medicine ,Gene duplication ,medicine ,Carcinoma ,Humans ,In patient ,Receptor, Fibroblast Growth Factor, Type 1 ,prognostic factor ,In Situ Hybridization, Fluorescence ,Aged ,Aged, 80 and over ,business.industry ,Fibroblast growth factor receptor 1 ,Smoking ,Hazard ratio ,Middle Aged ,Prognosis ,medicine.disease ,esophageal squamous cell carcinoma ,stomatognathic diseases ,Cardiothoracic surgery ,fluorescent in situ hybridization ,Carcinoma, Squamous Cell ,Female ,Clinical Research Paper ,Neoplasm Recurrence, Local ,business - Abstract
// Hyo Song Kim 1,* , Seung Eun Lee 2,* , Yoon Sung Bae 3,* , Dae Joon Kim 4 , Chang-Geol Lee 5 , Jin Hur 6 , Hyunsoo Chung 7 , Jun Chul Park 7 , Da Hyun Jung 7 , Sung Kwan Shin 7 , Sang Kil Lee 7 , Yong Chan Lee 7 , Hye Ryun Kim 1 , Yong Wha Moon 1 , Joo Hang Kim 1 , Young Mog Shim 8 , Susan S. Jewell 9 , Hyunki Kim 3 , Yoon-La Choi 2 and Byoung Chul Cho 1 1 Division of Medical Oncology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea 2 Departments of Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea 3 Department of Pathology, Yonsei University College of Medicine, Seoul, Korea 4 Department of Thoracic and Cardiovascular Surgery, Yonsei University College of Medicine, Seoul, Korea 5 Department of Radiation Oncology, Yonsei University College of Medicine, Seoul, Republic of Korea 6 Department of Radiology, Yonsei University College of Medicine, Seoul, Republic of Korea 7 Division of Gastroenterology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea 8 Department of Thoracic Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea 9 Abbott Molecular Laboratories, Des Plaines, IL * These authors contributed equally to this work as co-first authors Correspondence: Byoung Chul Cho, email: // Yoon-La Choi, email: // Hyunki Kim, email: // Keywords : Fibroblast growth factor receptor 1, esophageal squamous cell carcinoma, gene amplification, fluorescent in situ hybridization, prognostic factor Received : September 11, 2014 Accepted : December 09, 2014 Published : December 10, 2014 Abstract To investigate the frequency and the prognostic impact of fibroblast growth factor receptor 1 ( FGFR1 ) gene amplification in 526 curatively resected esophageal squamous cell carcinoma (ESCC). Using fluorescent in situ hybridization, high amplification was defined by an FGFR1 /centromer 8 ratio is ≥ 2.0, or average number of FGFR1 signals/tumor cell nucleus ≥ 6.0, or percentage of tumor cells containing ≥ 15 FGFR1 signals or large cluster in ≥ 10%. Low amplification was defined by ≥ 5 FGFR1 signals in ≥ 50%. FGFR2 and FGFR3 mutations were assessed by direct sequencing in 388 cases and no mutation was detected. High and low amplification were detected in 8.6% and 1.1%, respectively. High FGFR1 amplification had significantly shorter disease-free survival (34.0 vs 158.5 months P =0.019) and overall survival (52.2 vs not reached P =0.022) than low/no amplification group. After adjusting for sex, smoking, stage, histology, and adjuvant treatment, high FGFR1 amplification had a greater risk of recurrence (adjusted hazard ratio [AHR], 1.6; P =0.029) and death (AHR, 1.53; P =0.050). High amplification was significantly higher in current smokers than former and never-smokers ( P trend
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- 2014
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