Original Article
Modern Pathology advance online publication 2 October 2009; doi: 10.1038/modpathol.2009.123
Prognostic significance of histopathological tumor regression after neoadjuvant chemotherapy in esophageal adenocarcinomas
Rupert Langer1,5, Katja Ott2,5, Marcus Feith3, Florian Lordick4, Jörg-Rüdiger Siewert3 and Karen Becker1
- 1Institute of Pathology, Technische Universität München, München, Germany
- 2Department of Surgery, Universität Heidelberg, Heidelberg, Germany
- 3Department of Surgery, Klinikum Rechts der Isar, Technische Universität München, München, Germany
- 4Department of Medical Oncology, National Center for Tumor Diseases (NCT), Heidelberg, Germany
Correspondence: Dr R Langer, MD, Institute of Pathology, Klinikum Rechts der Isar, Technische Universität München, Trogerstrasse 18, D-81675 München, Germany. E-mail: rupert.langer@lrz.tu-muenchen.de
5These authors contributed equally to this work.
Received 2 March 2009; Revised 8 July 2009; Accepted 20 July 2009; Published online 2 October 2009.
Abstract
We evaluated histomorphological findings in 92 surgical resection specimens of locally advanced esophageal adenocarcinomas after neoadjuvant cisplatin-based chemotherapy. Tumor response to neoadjuvant chemotherapy was determined using a system encompassing three tumor regression grades based on the estimation of the percentage of residual tumor tissue of the primary tumor site in relation to the macroscopically identifiable previous tumor bed. The significance of this system was validated by correlation of the tumor regression grades with the corresponding clinicopathological characteristics and patient survival. Seven patients (7%) had complete tumor regression (grade tumor regression grade 1), 48 patients (52%) had subtotal or partial tumor regression (tumor regression grade 2: 1–50% residual tumor), and 37 patients (40%) had minimal or no regression (tumor regression grade 3: >50% residual tumor). Tumor regression was significantly associated with posttreatment complete tumor resection status (UICC R0 status; P=0.016), tumor category (UICC pT category; P<0.001), and with the absence of either lymph node metastases (P=0.001) or lymphatic invasion (P<0.001). Survival analysis showed a significant prognostic relevance of the applied regression system in univariate (P<0.001) and multivariate analyses as a single independent factor (P=0.024). We conclude that the effect of preoperative chemotherapy in esophageal adenocarcinomas can be assessed by the determination of histological tumor regression, providing highly valuable prognostic information, which may even exceed the prognostic impact of the current TNM classification of these tumors. Therefore, we strongly recommend the implementation of a standardized tumor regression grading system in pathological reports of esophageal adenocarcinomas treated by neoadjuvant chemotherapy.
Keywords:
adenocarcinoma, esophagus, regression, classification, chemotherapy

