Impact of T and N substage on survival and disease relapse in adjuvant rectal cancer: A pooled analysis

被引:96
作者
Gunderson, LL
Sargent, DJ
Tepper, JE
O'Connell, MJ
Allmer, C
Smalley, SR
Martenson, JA
Haller, DG
Mayer, RJ
Rich, TA
Ajani, JA
MacDonald, JS
Goldberg, RM
机构
[1] Mayo Clin Scottsdale, Ctr Canc, Dept Radiat Oncol, Scottsdale, AZ 85259 USA
[2] Mayo Clin, Canc Ctr Stat, Rochester, MN USA
[3] Mayo Clin, Dept Oncol, Rochester, MN USA
[4] Univ N Carolina, Dept Radiat Oncol, Chapel Hill, NC USA
[5] Kansas City Community Clin Oncol Program, Dept Radiat Oncol, Kansas City, MO USA
[6] Univ Penn, Dept Med Oncol, Philadelphia, PA 19104 USA
[7] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[8] Univ Virginia, Dept Radiat Oncol, Charlottesville, VA USA
[9] Univ Texas, MD Anderson Canc Ctr, Dept Med Oncol, Houston, TX 77030 USA
[10] St Vincents Comprehens Canc Ctr, Dept Med Oncol, New York, NY USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2002年 / 54卷 / 02期
关键词
rectal cancer; adjuvant chemoradiation; staging;
D O I
10.1016/S0360-3016(02)02945-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine the rates of survival and disease control by TNM and MAC stage in three randomized North American rectal adjuvant studies. Materials and Methods: Data were merged from 2551 eligible patients on NCCTG 79-47-51 (n = 200), NCCTG 86-47-51 (n = 656), and INT 114 (n = 1695). All patients received postoperative radiation, and 96% were randomized to receive concomitant and maintenance chemotherapy. Five-year follow-up was available in 94% of patients and 7-yr follow-up in 84%. Kaplan-Meier curves were used to estimate the distribution of overall survival (OS) and disease-free survival (DFS), and p values were derived using the log-rank test. Time to local and distant relapse was estimated using cumulative incidence methodology. Analyses were adjusted for treatment effect using Cox proportional hazards models. Results: OS and DFS were dependent on both TN stage and NT stage (N substage within T stage and T substage within N stage). Even among N2 patients (4 or more LN+), T stage influenced 5-yr OS (T1-2, 69%; T3, 48%; T4, 38%). Three risk groups of patients were defined: (1) intermediate: T3N0, T1-2N1; (2) moderately high: T4N0, T1-2N2, T3N1; and (3) high: T3N2, T4N1, T4N2. For Group 1, 5-yr OS was 74% and 81%, and 5-yr DFS was 66% and 74%. For Group 2, 5-yr OS ranged from 61% to 69%, and for Group 3, OS ranged from 33% to 48%. Cumulative incidence rates of local relapse and distant metastases revealed similar differences by TN and NT stage, as seen in the survival analyses. Conclusion: Patients with a single high-risk factor of either extension beyond the rectal wall (T3N0) or nodal involvement (T1-2N1) have improved OS, DFS, and disease control when compared to those with both high risk factors. Different treatment strategies may be indicated for intermediate- (T3N0, T1-2N1) vs. moderately high or high-risk patients in view of differential survival and rates of relapse. For future trial design, it may be preferable to perform separate studies, or a planned statistical analysis, for the "intermediate-risk" vs. the "moderately high" or "high-risk" subsets of patients. (C) 2002 Elsevier Science Inc.
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页码:386 / 396
页数:11
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