Eundong Park, Xin Wang, Michel Kmeid, Noureldien Darwish, Clifton G Fulmer, Nusret Bekir Subasi, Marcello P Toscano, Jing Zhou, Haiyan Qiu, Maciej Gracz, Xulang Zhang, Hwajeong Lee
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引用次数: 0
Abstract
Purpose: Prostate-specific membrane antigen (PSMA) is expressed in tumor-associated vessels of diverse malignancies, such as colorectal cancer (CRC). PSMA-targeted approaches show promise for diagnosing, treating, and assessing therapy response in non-prostatic cancer. Disease monitoring following neoadjuvant chemoradiation (CRT) is especially important in rectal cancer.
Methods: Firstly, clinical and histologic features of untreated CRC (n = 237; 54 from rectum) were examined for their association with PSMA expression. Secondly, rectal cancer cases following neoadjuvant CRT (n = 45) were retrieved to assess the relationship between PSMA expression, downstaging, and tumor volume reduction and were compared with untreated rectal cancers (n = 54).
Results: In untreated CRC, PSMA expression was negatively associated with pTNM stage, pT stage, pN stage, tumor deposit presence and count, and post-op adjuvant therapy administration. Higher PSMA expression was correlated with shorter overall survival when pTNM stage was controlled. In the treated rectal cancer group, advanced pTNM stage was associated with a reduced PSMA expression. In addition, treated rectal cancers showed lower PSMA expression than untreated rectal cancers. While PSMA levels correlated with tumor volume reduction and downstaging following CRT, this association was lost in stage-matched analysis.
Conclusion: PSMA expression was lower in more advanced CRCs, and the trend persisted in treated rectal cancer. After adjusting for pTNM stage, higher PSMA expression was predictive of reduced overall survival. Post-CRT PSMA level was associated with downstaging and pathologic tumor volume reduction in rectal cancer. Further studies are needed to assess the clinical value of PSMA-directed approaches in CRC management.
期刊介绍:
The Journal of Gastrointestinal Cancer is a multidisciplinary medium for the publication of novel research pertaining to cancers arising from the gastrointestinal tract.The journal is dedicated to the most rapid publication possible.The journal publishes papers in all relevant fields, emphasizing those studies that are helpful in understanding and treating cancers affecting the esophagus, stomach, liver, gallbladder and biliary tree, pancreas, small bowel, large bowel, rectum, and anus. In addition, the Journal of Gastrointestinal Cancer publishes basic and translational scientific information from studies providing insight into the etiology and progression of cancers affecting these organs. New insights are provided from diverse areas of research such as studies exploring pre-neoplastic states, risk factors, epidemiology, genetics, preclinical therapeutics, surgery, radiation therapy, novel medical therapeutics, clinical trials, and outcome studies.In addition to reports of original clinical and experimental studies, the journal also publishes: case reports, state-of-the-art reviews on topics of immediate interest or importance; invited articles analyzing particular areas of pancreatic research and knowledge; perspectives in which critical evaluation and conflicting opinions about current topics may be expressed; meeting highlights that summarize important points presented at recent meetings; abstracts of symposia and conferences; book reviews; hypotheses; Letters to the Editors; and other items of special interest, including:Complex Cases in GI Oncology: This is a new initiative to provide a forum to review and discuss the history and management of complex and involved gastrointestinal oncology cases. The format will be similar to a teaching case conference where a case vignette is presented and is followed by a series of questions and discussion points. A brief reference list supporting the points made in discussion would be expected.