TY - JOUR
T1 - Significance of histopathological tumor regression after neoadjuvant chemotherapy in gastric adenocarcinomas
T2 - A summary of 480 cases
AU - Becker, Karen
AU - Langer, Rupert
AU - Reim, Daniel
AU - Novotny, Alexander
AU - Meyer Zum Buschenfelde, Christian
AU - Engel, Jutta
AU - Friess, Helmut
AU - Hofler, Heinz
PY - 2011/5
Y1 - 2011/5
N2 - Objective: An increasing number of patients with locally advanced gastric carcinomas (GC) are being treated with preoperative chemotherapy before surgery. Background: Histopathological tumor regression may have an important prognostic impact in addition to the UICC-TNM classification system. Methods: We evaluated the histopathological tumor regression in 480 surgical resection specimens of GC after neoadjuvant cisplatin-based chemotherapy, using an established system encompassing three tumor regression grades based on the estimation of the percentage of residual tumor tissue at the primary tumor site in relation to the macroscopically identifiable former tumor bed. Tumor regression was correlated to clinicopathological characteristics and patient survival. Results: Of the patients in this study, 102 (21.2%) had complete or subtotal tumor regression (<10% residual tumor), 121 (25.2%) had partial tumor regression (10-50% residual tumor), and 257 (53.5%) had minimal or no regression (>50% residual tumor). Tumor regression was significantly associated with posttreatment tumor category (pT), lymph node status (pN), lymphatic invasion status (pL), and resection status (P < 0.001). Major histopathological regression was less frequent in tumors of the distal stomach and tumors of nonintestinal type (P = 0.003). Tumor regression (P = 0.009) and postoperative Lymph node status (P < 0.001) were independent prognostic factors for survival in a multivariate analysis of tumor regression, ypT/N/L category, resection status, grading and Lauren's classification. Conclusions: Assessment of histological tumor regression after preoperative chemotherapy in GC provides objective and highly valuable prognostic information in addition to posttherapeutic lymph node status. A standardized tumor regression grading system should be implemented in pathological reports of these tumors.
AB - Objective: An increasing number of patients with locally advanced gastric carcinomas (GC) are being treated with preoperative chemotherapy before surgery. Background: Histopathological tumor regression may have an important prognostic impact in addition to the UICC-TNM classification system. Methods: We evaluated the histopathological tumor regression in 480 surgical resection specimens of GC after neoadjuvant cisplatin-based chemotherapy, using an established system encompassing three tumor regression grades based on the estimation of the percentage of residual tumor tissue at the primary tumor site in relation to the macroscopically identifiable former tumor bed. Tumor regression was correlated to clinicopathological characteristics and patient survival. Results: Of the patients in this study, 102 (21.2%) had complete or subtotal tumor regression (<10% residual tumor), 121 (25.2%) had partial tumor regression (10-50% residual tumor), and 257 (53.5%) had minimal or no regression (>50% residual tumor). Tumor regression was significantly associated with posttreatment tumor category (pT), lymph node status (pN), lymphatic invasion status (pL), and resection status (P < 0.001). Major histopathological regression was less frequent in tumors of the distal stomach and tumors of nonintestinal type (P = 0.003). Tumor regression (P = 0.009) and postoperative Lymph node status (P < 0.001) were independent prognostic factors for survival in a multivariate analysis of tumor regression, ypT/N/L category, resection status, grading and Lauren's classification. Conclusions: Assessment of histological tumor regression after preoperative chemotherapy in GC provides objective and highly valuable prognostic information in addition to posttherapeutic lymph node status. A standardized tumor regression grading system should be implemented in pathological reports of these tumors.
UR - http://www.scopus.com/inward/record.url?scp=79954462482&partnerID=8YFLogxK
U2 - 10.1097/SLA.0b013e318216f449
DO - 10.1097/SLA.0b013e318216f449
M3 - Article
C2 - 21490451
AN - SCOPUS:79954462482
SN - 0003-4932
VL - 253
SP - 934
EP - 939
JO - Annals of Surgery
JF - Annals of Surgery
IS - 5
ER -