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Clinical stage after preoperative chemoradiation is a better predictor of patient outcome than the baseline stage for localized gastric cancer
被引:22
|作者:
Patel, Pooja R.
Mansfield, Paul F.
Crane, Christopher H.
Wu, Tsung-Teh
Lee, Jeffrey H.
Lynch, Patrick M.
Morris, Jeffrey
Pisters, Peter W.
Feig, Barry
Sunder, Punita K.
Izzo, Julie G.
Ajani, Jaffer A.
机构:
[1] Univ Texas, MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
[4] Univ Texas, MD Anderson Canc Ctr, Dept Clin Pathol, Houston, TX 77030 USA
[5] Univ Texas, MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
来源:
关键词:
gastric cancer;
surgery;
preoperative chemoradiation;
disease-free survival;
overall survival;
D O I:
10.1002/cncr.22870
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
BACKGROUND. For patients with localized gastric cancer (LGC) who are receiving 2 preoperative chemoradiation (CTRT), the postsurgical pathologic stage predicts overall survival (OS) better than the baseline stage. The authors hypothesized 4 that presurgical (postCTRT) stage would also correlate better with patient outcome than the baseline stage. METHODS. The authors analyzed 74 LGC patients treated with preoperative CTRT receiving similar treatment. Patients were staged with baseline endoscopic ultrasonography (EUS) and laparoscopy. Patients received induction chemotherapy, then CTRT (45 Gy), and had an attempted surgery. After CTRT, patients had complete preoperative staging including EUS in 35 patients. RESULTS. Thirty-five had all 3 sets of staging, baseline, presurgical, and postsurgical. Baseline stage did not associate with OS (P =.16) nor disease-tree survival (DFS; P =.13). However, presurgical stage was associated with OS (P =.01), and DFS (P=.05). OS was also associated with postsurgical stage and was longer for stages 0 and I than for stages III and IV (P =.01 and .04, respectively). Similarly, DFS was longer in postsurgical pathologic stages 0, 1, and 11 than in stage III or IV (P <.001, <.001, and <.01, respectively). Baseline staging did not correlate with the proportion of patients alive at 4 years; however, presurgical staging did. Patients with stage I or 11 survived longer than those with stage III or IV (81% vs 25%; P <.01). CONCLUSIONS. Heterogeneity in clinical biology of LGC is best reflected after CTRT in presurgical and postsurgical pathologic stages rather than by the baseline stage. Correlation of outcome with presurgical staging may facilitate strategies to individualize therapy for LGC. Cancer 2007; 110:989-95. (c) 2007 American Cancer Society
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页码:989 / 995
页数:7
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