Gunderson Leonard L, Sargent Daniel J, Tepper Joel E, O'Connell Michael J, Allmer Cristine, Smalley Steven R, Martenson James A, Haller Daniel G, Mayer Robert J, Rich Tyvin A, Ajani Jaffer A, Macdonald John S, Goldberg Richard M
Department of Radiation Oncology, Mayo Clinic Scottsdale, Scottsdale, AZ 85259, USA.
Int J Radiat Oncol Biol Phys. 2002 Oct 1;54(2):386-96. doi: 10.1016/s0360-3016(02)02945-0.
To determine the rates of survival and disease control by TNM and MAC stage in three randomized North American rectal adjuvant studies.
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.
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.
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.
在三项北美直肠癌辅助治疗随机研究中,确定按TNM和MAC分期的生存率及疾病控制率。
合并了来自NCCTG 79 - 47 - 51(n = 200)、NCCTG 86 - 47 - 51(n = 656)和INT 114(n = 1695)的2551例符合条件患者的数据。所有患者均接受术后放疗,96%的患者被随机分配接受同步和维持化疗。94%的患者有5年随访数据,84%的患者有7年随访数据。采用Kaplan - Meier曲线估计总生存期(OS)和无病生存期(DFS)的分布,并使用对数秩检验得出p值。采用累积发病率方法估计局部和远处复发时间。使用Cox比例风险模型对治疗效果进行分析调整。
OS和DFS均取决于TN分期和NT分期(T期内的N亚分期以及N期内的T亚分期)。即使在N2患者(4个或更多淋巴结阳性)中,T分期也影响5年OS(T1 - 2期为69%;T3期为48%;T4期为38%)。定义了三组风险患者:(1)中度风险:T3N0、T1 - 2N1;(2)中度高风险:T4N0、T1 - 2N2、T3N1;(3)高风险:T3N2、T4N1、T4N2。对于第1组,5年OS为74%和81%,5年DFS为66%和74%。对于第2组,5年OS为61%至69%,对于第3组,OS为33%至48%。局部复发和远处转移的累积发病率在TN和NT分期上显示出类似差异,如生存分析中所见。
与具有两个高风险因素的患者相比,仅具有一个高风险因素(直肠壁外侵犯(T3N0)或淋巴结受累(T1 - 2N1))的患者在OS、DFS和疾病控制方面有所改善。鉴于生存差异和复发率不同,对于中度风险(T3N0、T1 - 2N1)与中度高风险或高风险患者可能需要不同的治疗策略。对于未来的试验设计,对“中度风险”与“中度高风险”或“高风险”患者亚组分别进行研究或进行计划好的统计分析可能更为可取。