PMID- 23715160 OWN - NLM STAT- MEDLINE DCOM- 20130815 LR - 20130618 IS - 1532-0979 (Electronic) IS - 0147-5185 (Linking) VI - 37 IP - 7 DP - 2013 Jul TI - Postoperative nodal status and diffuse-type histology are independent prognostic factors in resectable advanced gastric carcinomas after preoperative chemotherapy. PG - 1022-9 LID - 10.1097/PAS.0b013e31828778fd [doi] AB - Surgical resection of primary gastric lesions after neoadjuvant or palliative chemotherapy is performed for curative or palliative purpose in locally advanced (LA) or initially metastatic (IM) gastric cancer. We investigated which histomorphologic features were associated with patient prognosis. We examined 143 patients (57 LA and 86 IM) who underwent gastrectomy after chemotherapy between 2000 and 2009. The tumor regression grade (TRG)-determined by examining the residual neoplastic cells and background stromal changes-was evaluated. Progression-free (PFS) and overall survival (OS) were evaluated according to pretherapeutic and posttherapeutic clinicopathologic factors using univariate and multivariate analyses. Because both the LA and the IM groups showed similar trends of PFS and OS according to TRG, the 2 groups were analyzed together. Patients with TRG1 (no residual primary tumor) showed a superior PFS and OS than the remaining TRGs. We defined pathologic complete regression (pCR) as TRG1 with negative lymph nodes (LN) and the others as non-pCR. Sixteen patients (11.1%) had pCR with better PFS (P=0.007) and OS (P=0.006). Initial disease status (LA or IM) remained as independent prognostic factors for PFS (P=0.021) but not for OS (P=0.109). The postoperative negative LN status correlated with good outcome and postoperative diffuse-type histology correlated with poor outcome after multivariate analysis. This study showed that pCR, but not partial regression, provides meaningful prognostic information in gastrectomy after chemotherapy. In addition, postoperative LN positivity and diffuse-type histology were independent poor prognostic factors for PFS and OS. FAU - Koh, Young Wha AU - Koh YW AD - Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea. FAU - Park, Young Soo AU - Park YS FAU - Ryu, Min-Hee AU - Ryu MH FAU - Ryoo, Baek-Yeol AU - Ryoo BY FAU - Park, Hye Jin AU - Park HJ FAU - Yook, Jeong Hwan AU - Yook JH FAU - Kim, Byung Sik AU - Kim BS FAU - Kang, Yoon-Koo AU - Kang YK LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Am J Surg Pathol JT - The American journal of surgical pathology JID - 7707904 SB - IM MH - Adenocarcinoma/mortality/*secondary/therapy MH - Adult MH - Aged MH - Antineoplastic Combined Chemotherapy Protocols/*therapeutic use MH - Chemotherapy, Adjuvant/*methods MH - Disease-Free Survival MH - Female MH - Gastrectomy MH - Humans MH - Lymph Nodes/*pathology MH - Male MH - Middle Aged MH - Neoadjuvant Therapy/*methods MH - Postoperative Period MH - Prognosis MH - Republic of Korea/epidemiology MH - Retrospective Studies MH - Stomach Neoplasms/mortality/*pathology/therapy MH - Survival Rate EDAT- 2013/05/30 06:00 MHDA- 2013/08/16 06:00 CRDT- 2013/05/30 06:00 PHST- 2013/05/30 06:00 [entrez] PHST- 2013/05/30 06:00 [pubmed] PHST- 2013/08/16 06:00 [medline] AID - 10.1097/PAS.0b013e31828778fd [doi] PST - ppublish SO - Am J Surg Pathol. 2013 Jul;37(7):1022-9. doi: 10.1097/PAS.0b013e31828778fd.