Prognostic Significance of Tumor Regression After Preoperative Chemoradiotherapy for Rectal Cancer

Author:

Rödel Claus1,Martus Peter1,Papadoupolos Thomas1,Füzesi Laszlo1,Klimpfinger Martin1,Fietkau Rainer1,Liersch Torsten1,Hohenberger Werner1,Raab Rudolf1,Sauer Rolf1,Wittekind Christian1

Affiliation:

1. From the Department of Radiation Therapy, Department of Surgery, and Institute of Pathology, University of Erlangen, Erlangen; Institute of Medical Informatics, Biometry and Epidemiology, Charité University Medicine, Berlin; Department of Pathology, University Hospital Göttingen; Germany Department of Surgery, University of Göttingen, Göttingen; Department of Radiation Therapy, University of Rostock, Rostock; Department of Surgery, Klinikum Oldenburg, Oldenburg; Institute of Pathology, University of...

Abstract

Purpose We assessed the impact of tumor regression grading (TRG) and its value in correlation to established prognostic factors in a cohort of rectal carcinoma patients treated by preoperative chemoradiotherapy (CRT). Patients and Methods TRG was evaluated on surgical specimens of 385 patients treated within the preoperative CRT arm of the CAO/ARO/AIO-94 trial: 50.4 Gy was delivered, fluorouracil was given in the first and fifth week, and surgery was performed 6 weeks thereafter. TRG was determined by the amount of viable tumor versus fibrosis, ranging from TRG 4 when no viable tumor cells were detected, to TRG 0 when fibrosis was completely absent. TRG 3 was defined as regression more than 50% with fibrosis outgrowing the tumor mass, TRG 2 was defined as regression less than 50%, and TRG 1 was defined basically as a morphologically unaltered tumor mass. We performed an initially unplanned, hypothesis-generating analysis with respect to the prognostic value of this TRG system. Results TRG 4, 3, 2, 1, 0 was found in 10.4%, 52.2%, 13.8%, 15.3%, and 8.3% of the resected specimens, respectively. Five-year disease-free survival (DFS) after CRT and curative resection was 86% for TRG 4, 75% for grouped TRG 2 + 3, and 63% for grouped TRG 0 + 1 (P = .006). On multivariate analysis, the pathologic T category and the nodal status after CRT were the most important independent prognostic factors for DFS. Conclusion In this exploratory analysis, complete (TRG 4) and intermediate pathologic response (TRG 2 + 3) suggested improved DFS after preoperative CRT. TRG assessment should be implemented in pathologic evaluation and prospectively validated in further studies.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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