PMID- 21300482 OWN - NLM STAT- MEDLINE DCOM- 20120316 LR - 20220331 IS - 1879-355X (Electronic) IS - 0360-3016 (Linking) VI - 82 IP - 2 DP - 2012 Feb 1 TI - Stage-to-stage comparison of preoperative and postoperative chemoradiotherapy for T3 mid or distal rectal cancer. PG - 856-62 LID - 10.1016/j.ijrobp.2010.10.079 [doi] AB - PURPOSE: To investigate, in a comparative analysis, the prognostic implications of postchemoradiotherapy (post-CRT) pathologic stage (ypStage) vs. postoperative pathologic stage (pStage) in rectal cancer. METHODS AND MATERIALS: Between May 2001 and December 2006, 487 patients with T3 mid or distal rectal cancer were analyzed retrospectively. Concurrent CRT was administered preoperatively (n = 364, 74.7%) or postoperatively (n = 123, 25.3%). The radiation dose was 50.4 Gy in 28 fractions. All patients underwent a total mesorectal excision and received adjuvant chemotherapy. Disease-free survival (DFS) was estimated using the Kaplan-Meier method. Differences in DFS, stratified by ypStage and pStage, were compared using the log-rank test. RESULTS: For surviving patients, the median follow-up period was 68 months (range, 12-105 months). The 5-year local recurrence-free survival rate was not different, at 95.3% and 92.1% in preoperative and postoperative CRT groups, respectively (p = 0.402), but the 5-year distant metastasis-free survival rate was significantly different, at 81.6% (preoperative CRT) vs. 65.4% (postoperative CRT; p = 0.001). The 5-year DFS rate of 78.8% in the preoperative CRT group was significantly better than the 63.0% rate in the postoperative CRT group (p = 0.002). Post-CRT pathologic Stage 0-I occurred in 42.6% (155 of 364) of the patients with preoperative CRT. The 5-year DFS rates were 90.2% (ypStage 0-I), 83.5% (ypStage II), 77.3% (pStage II), 58.6% (ypStage III), and 54.7% (pStage III). The DFS rate of ypStage 0-I was significantly better than that of ypStage II or pStage II. Post-CRT pathologic Stage II and III had similar DFS, compared with pStage II and III, respectively. CONCLUSIONS: Disease-free survival predicted by each ypStage was similar to that predicted by the respective pStage. Improved DFS with preoperative vs. postoperative CRT was associated with the ypStage 0-I group that showed a similarly favorable outcome to pStage I rectal cancer. CI - Copyright (c) 2012 Elsevier Inc. All rights reserved. FAU - Yeo, Seung-Gu AU - Yeo SG AD - Center for Colorectal Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Korea. FAU - Kim, Dae Yong AU - Kim DY FAU - Park, Ji Won AU - Park JW FAU - Choi, Hyo Seong AU - Choi HS FAU - Oh, Jae Hwan AU - Oh JH FAU - Kim, Sun Young AU - Kim SY FAU - Chang, Hee Jin AU - Chang HJ FAU - Kim, Tae Hyun AU - Kim TH FAU - Sohn, Dae Kyung AU - Sohn DK LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20110206 PL - United States TA - Int J Radiat Oncol Biol Phys JT - International journal of radiation oncology, biology, physics JID - 7603616 RN - 0W860991D6 (Deoxycytidine) RN - 6804DJ8Z9U (Capecitabine) RN - 7673326042 (Irinotecan) RN - Q573I9DVLP (Leucovorin) RN - U3P01618RT (Fluorouracil) RN - XT3Z54Z28A (Camptothecin) SB - IM MH - Adenocarcinoma/mortality/*pathology/*therapy MH - Antineoplastic Combined Chemotherapy Protocols/therapeutic use MH - Camptothecin/administration & dosage/analogs & derivatives MH - Capecitabine MH - Chemoradiotherapy/*methods/mortality MH - Chemotherapy, Adjuvant/methods MH - Deoxycytidine/administration & dosage/analogs & derivatives MH - Disease-Free Survival MH - Dose Fractionation, Radiation MH - Drug Administration Schedule MH - Female MH - Fluorouracil/administration & dosage/analogs & derivatives MH - Humans MH - Irinotecan MH - Leucovorin/administration & dosage MH - Male MH - Middle Aged MH - Neoplasm Staging/methods MH - Postoperative Period MH - Preoperative Period MH - Prognosis MH - Rectal Neoplasms/mortality/*pathology/*therapy MH - Retrospective Studies MH - Survival Rate MH - Time Factors EDAT- 2011/02/09 06:00 MHDA- 2012/03/17 06:00 CRDT- 2011/02/09 06:00 PHST- 2010/06/12 00:00 [received] PHST- 2010/09/17 00:00 [revised] PHST- 2010/10/20 00:00 [accepted] PHST- 2011/02/09 06:00 [entrez] PHST- 2011/02/09 06:00 [pubmed] PHST- 2012/03/17 06:00 [medline] AID - S0360-3016(10)03701-6 [pii] AID - 10.1016/j.ijrobp.2010.10.079 [doi] PST - ppublish SO - Int J Radiat Oncol Biol Phys. 2012 Feb 1;82(2):856-62. doi: 10.1016/j.ijrobp.2010.10.079. Epub 2011 Feb 6.