Tumour regression grade (TRG) analyses in patients with resectable gastro-oesophageal adenocarcinomas treated with platinum-based neoadjuvant chemotherapy.

Histopathology

Laboratory of Molecular Oncology, Academic Unit of Oncology, School of Molecular Medical Sciences, Faculty of Medicine & Health Sciences, University of Nottingham, Nottingham, UK.

Published: October 2009

AI Article Synopsis

  • Neoadjuvant chemotherapy is the go-to treatment for gastro-oesophageal adenocarcinoma, and this study aimed to confirm the effectiveness of tumor regression grade (TRG) in predicting treatment response and potential use in future biomarker research.
  • Three blinded pathologists evaluated various tumor characteristics revealing that a significantly higher percentage of patients who received chemotherapy had a favorable TRG (grades 1, 2, or 3) compared to those who underwent primary surgery.
  • The study found that patients responding well to chemotherapy (lower TRG) exhibited significant tumor downstaging, particularly in gastric cancers, suggesting improved outcomes linked to TRG evaluation.

Article Abstract

Aims: Neoadjuvant chemotherapy followed by surgery is the standard of care for patients with gastro-oesophageal adenocarcinoma. The aims were to validate the utility of the tumour regression grade (TRG) in patients who have received chemotherapy and to investigate if (i) TRG correlates with tumour downstaging and (ii) TRG could provide a comparative platform for future predictive biomarker investigations.

Methods And Results: Three pathologists were blinded to the treatment approaches. Review included diagnosis, tumour grade, TNM staging, vascular invasion, perineural invasion, resection margin involvement and histopathological response to chemotherapy, as measured by TRG. In the neoadjuvant chemotherapy (CS) group (n = 84), 46.7% of gastric/gastro-oesophageal junction adenocarcinomas, and 45.5% of lower third oesophageal adenocarcinomas had TRG 1, 2 or 3 compared with 13.7% in the primary surgery group (n = 124) (P < 0.001 and P = 0.006, respectively). In the CS group, responders (TRG 1, 2 or 3) showed significant tumour downstaging [early ypT-stage disease (P = 0.002)]. In gastric cancers specifically, additional associations were seen with negative nodal disease (P = 0.044) and absence of vascular invasion (P = 0.027).

Conclusions: TRG may reflect response to chemotherapy. In addition, positive correlations between TRG and ypTNM staging were demonstrated that would suggest tumour downstaging.

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Source
http://dx.doi.org/10.1111/j.1365-2559.2009.03404.xDOI Listing

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