Clinical and molecular characteristics of early-onset vs average-onset esophagogastric cancer

Author:

Lumish Melissa A12ORCID,Walch Henry34ORCID,Maron Steven B12,Chatila Walid34ORCID,Kemel Yelena5ORCID,Maio Anna5,Ku Geoffrey Y12ORCID,Ilson David H12ORCID,Won Elizabeth12ORCID,Li Jia12,Joshi Smita S12,Gu Ping12,Schattner Mark A6,Laszkowska Monika6ORCID,Gerdes Hans6,Jones David R7,Sihag Smita7,Coit Daniel G7ORCID,Tang Laura H8,Strong Vivian E7,Molena Daniela7,Stadler Zsofia K125,Schultz Nikolaus34,Janjigian Yelena Y12,Cercek Andrea12ORCID

Affiliation:

1. Memorial Sloan Kettering Cancer Center Gastrointestinal Oncology Service, Department of Medicine, , New York, NY, USA

2. Weill Cornell Medical College Department of Medicine, , New York, NY, USA

3. Memorial Sloan Kettering Cancer Center Computational Oncology, Department of Epidemiology and Biostatistics, , New York, NY, USA

4. Memorial Sloan Kettering Cancer Center Marie-Josée and Henry R. Kravis Center for Molecular Oncology, , New York, NY, USA

5. Memorial Sloan Kettering Cancer Center Robert and Kate Niehaus Center for Inherited Cancer Genomics, , New York, NY, USA

6. Memorial Sloan Kettering Cancer Center Gastroenterology, Hepatology and Nutrition Service, Department of Medicine, , New York, NY, USA

7. Sloan Kettering Cancer Center Department of Surgery Memorial, , New York, NY, USA

8. Memorial Sloan Kettering Cancer Center Department of Pathology, , New York, NY, USA

Abstract

Abstract Background The rate of esophagogastric cancer is rising among individuals under 50 years of age. It remains unknown whether early-onset esophagogastric cancer represents a unique entity. This study investigated the clinical and molecular characteristics of early-onset and average-onset esophagogastric cancer . Methods We reviewed the Memorial Sloan Kettering Cancer Center gastric, esophageal, and gastroesophageal junction cancer database. Associations between baseline characteristics and tumor and germline molecular alterations were compared between those with early-onset and average-onset esophagogastric cancer using Fisher exact tests and the Benjamini-Hochberg method for multiple-hypothesis correction. Results We included 1123 patients with early-onset esophagogastric cancer (n = 219; median age = 43 years [range = 18-49 years]) and average-onset esophagogastric cancer (n = 904; median age = 67 years [range = 50-94 years]) treated between 2005 and 2018. The early-onset group had more women (39% vs 28%, P = .002). Patients with early-onset esophagogastric cancer were more likely to have a gastric primary site (64% vs 44%, P < .0001). The signet ring cell and/or diffuse type was 3 times more common in the early-onset esophagogastric cancer group (31% vs 9%, P < .0001). Early-onsite tumors were more frequently genomically stable (31% vs 18%, P = .0002) and unlikely to be microsatellite instability high (2% vs 7%, P = .003). After restricting to adenocarcinoma and signet ring cell and/or diffuse type carcinomas, we observed no difference in stage (P = .40) or overall survival from stage IV diagnosis (median = 22.7 vs 22.1 months, P = .78). Conclusions Our study supported a preponderance of gastric primary disease sites, signet ring histology, and genomically stable molecular subtypes in early-onset esophagogastric cancer. Our findings highlight the need for further research to define the underlying pathogenesis and strategies for early detection and prevention.

Funder

Conquer Cancer

ASCO Foundation

Young Investigator Award

Tow Center for Developmental Oncology Career Development Award

National Institutes of Health

National Cancer Institute

Memorial Sloan Kettering Cancer Center

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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