TY - JOUR
T1 - Development and Validation of an Easy-to-Implement, Practical Algorithm for the Identification of Molecular Subtypes of Gastric Cancer
T2 - Prognostic and Therapeutic Implications
AU - Koh, Jiwon
AU - Lee, Keun Wook
AU - Nam, Soo Kyung
AU - Seo, An Na
AU - Kim, Ji Won
AU - Kim, Jin Won
AU - Park, Do Joong
AU - Kim, Hyung Ho
AU - Kim, Woo Ho
AU - Lee, Hye Seung
N1 - Publisher Copyright:
© AlphaMed Press 2019
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Background: Gastric cancer (GC) is a heterogeneous disease, and substantial efforts have been made to develop a molecular biology-based classification system for GC. Analysis of the genomic signature is not always feasible, and thus, we aimed to (i) develop and validate a practical immunohistochemistry (IHC)- and polymerase chain reaction (PCR)-based molecular classification of GC and (ii) to assess HER2 status according to this classification. Materials and Methods: A total of 894 consecutive patients with GC from two individual cohorts (training, n = 507; validation, n = 387) were classified using Epstein-Barr virus (EBV) in situ hybridization, microsatellite instability (MSI) testing, and IHC for E-cadherin and p53. Results: We were able to classify patients into five groups in the training cohort: group 1 (MSI+), group 2 (EBV−, MSI−, non-epithelial-mesenchymal transition [non-EMT]-like, p53−), group 3 (EBV+), group 4 (EBV−, MSI−, non-EMT-like, p53+), and group 5 (EBV−, MSI−, EMT-like). In the training cohort, each group showed different overall survival (OS) after gastrectomy (p <.001); group 1 had the best prognosis, and group 5 showed the worst survival outcome. The significant impact of the classification system on OS was also verified in the validation cohort (p =.004). HER2 positivity was observed in 6.5% of total population, and most of HER2-positive cases (93.1%) were included in groups 2 and 4. Conclusion: We developed and validated a modified IHC- and PCR-based molecular classification system in GC, which showed significant impact on survival, irrespective of stage or other clinical variables. We also found close association between HER2 status and non-EMT phenotype in our classification system. Implications for Practice: Molecular classification of gastric cancer suggested by previous studies mostly relies on extensive genomic data analysis, which is not always available in daily practice. The authors developed a simplified immunohistochemistry- and polymerase chain reaction-based molecular classification of gastric cancer and proved the prognostic significance of this classification, as well as the close association between HER2 status and certain groups of the classification, in the largest consecutive cohort of gastric cancer. Results of this study suggest that this scheme is a cost-effective, easy-to-implement, and feasible way of classifying gastric cancer in daily clinical practice, also serving as a practical tool for aiding therapeutic decisions and predicting prognosis.
AB - Background: Gastric cancer (GC) is a heterogeneous disease, and substantial efforts have been made to develop a molecular biology-based classification system for GC. Analysis of the genomic signature is not always feasible, and thus, we aimed to (i) develop and validate a practical immunohistochemistry (IHC)- and polymerase chain reaction (PCR)-based molecular classification of GC and (ii) to assess HER2 status according to this classification. Materials and Methods: A total of 894 consecutive patients with GC from two individual cohorts (training, n = 507; validation, n = 387) were classified using Epstein-Barr virus (EBV) in situ hybridization, microsatellite instability (MSI) testing, and IHC for E-cadherin and p53. Results: We were able to classify patients into five groups in the training cohort: group 1 (MSI+), group 2 (EBV−, MSI−, non-epithelial-mesenchymal transition [non-EMT]-like, p53−), group 3 (EBV+), group 4 (EBV−, MSI−, non-EMT-like, p53+), and group 5 (EBV−, MSI−, EMT-like). In the training cohort, each group showed different overall survival (OS) after gastrectomy (p <.001); group 1 had the best prognosis, and group 5 showed the worst survival outcome. The significant impact of the classification system on OS was also verified in the validation cohort (p =.004). HER2 positivity was observed in 6.5% of total population, and most of HER2-positive cases (93.1%) were included in groups 2 and 4. Conclusion: We developed and validated a modified IHC- and PCR-based molecular classification system in GC, which showed significant impact on survival, irrespective of stage or other clinical variables. We also found close association between HER2 status and non-EMT phenotype in our classification system. Implications for Practice: Molecular classification of gastric cancer suggested by previous studies mostly relies on extensive genomic data analysis, which is not always available in daily practice. The authors developed a simplified immunohistochemistry- and polymerase chain reaction-based molecular classification of gastric cancer and proved the prognostic significance of this classification, as well as the close association between HER2 status and certain groups of the classification, in the largest consecutive cohort of gastric cancer. Results of this study suggest that this scheme is a cost-effective, easy-to-implement, and feasible way of classifying gastric cancer in daily clinical practice, also serving as a practical tool for aiding therapeutic decisions and predicting prognosis.
KW - Epithelial-mesenchymal transition
KW - Gastric cancer
KW - Microsatellite instability
KW - Molecular classification
KW - Prognosis
UR - http://www.scopus.com/inward/record.url?scp=85070104354&partnerID=8YFLogxK
U2 - 10.1634/theoncologist.2019-0058
DO - 10.1634/theoncologist.2019-0058
M3 - Article
C2 - 31371521
AN - SCOPUS:85070104354
SN - 1083-7159
VL - 24
SP - e1321-e1330
JO - Oncologist
JF - Oncologist
IS - 12
ER -