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
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.
引用
收藏
页码:386 / 396
页数:11
相关论文
共 50 条
  • [1] Impact of T and N stage and treatment on survival and relapse in adjuvant rectal cancer: A pooled analysis
    Gunderson, LL
    Sargent, DJ
    Tepper, JE
    Wolmark, N
    O'Connell, MJ
    Begovic, M
    Allmer, C
    Colangelo, L
    Smalley, SR
    Haller, DG
    Martenson, JA
    Mayer, RJ
    Rich, TA
    Ajani, JA
    MacDonald, JS
    Willett, CG
    Goldberg, RM
    JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (10) : 1785 - 1796
  • [2] Adjuvant radiochemotherapy of rectal cancer:: Retrospective study of survival rate, relapse rate and toxicity
    Küchenmeister, U
    Fietkau, R
    STRAHLENTHERAPIE UND ONKOLOGIE, 2002, 178 : 27 - 27
  • [3] Impact on overall survival and disease-free survival of adjuvant chemotherapy after neoadjuvant chemoradiotherapy for rectal cancer
    de Castro, Rafael Amaral
    Paiva, Carlos Eduardo
    Saad-Hossne, Rogerio
    Michelin, Odair Carlito
    Souza, Cristiano de Padua
    JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (15)
  • [4] Impact of adjuvant chemotherapy on survival in ypT0-2 N0 rectal cancer
    Alorabi, Mohamed Osama
    Gouda, Abdelrahman
    Abdeen, Mohammed
    Said, Ahmed
    Abdelaal, Moamen
    Eid, Reem
    Yahia, Maha
    INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 2025, 40 (01)
  • [5] Impact of robotic learning curve on histopathology in rectal cancer: A pooled analysis
    Gachabayov, Mahir
    Kim, Seon-Hahn
    Jimenez-Rodriguez, Rosa
    Kuo, Li-Jen
    Cianchi, Fabio
    Tulina, Inna
    Tsarkov, Petr
    Bergamaschi, Roberto
    SURGICAL ONCOLOGY-OXFORD, 2020, 34 : 121 - 125
  • [6] The impact of T and N stage on long-term survival of rectal cancer patients in the community
    Kozak, Kevin R.
    Moody, John S.
    JOURNAL OF SURGICAL ONCOLOGY, 2008, 98 (03) : 161 - 166
  • [7] POSTOPERATIVE ADJUVANT THERAPY OF RECTAL-CANCER - AN ANALYSIS OF DISEASE-CONTROL, SURVIVAL, AND PROGNOSTIC FACTORS
    SCHILD, SE
    MARTENSON, JA
    GUNDERSON, LL
    ILSTRUP, DM
    BERG, KK
    OCONNELL, MJ
    WEILAND, LH
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1989, 17 (01): : 55 - 62
  • [8] Impact of neoadjuvant and adjuvant radiotherapy on disease-specific survival in patients with stages II-IV rectal cancer
    Wu, Yinying
    Liu, Haiyang
    Du, Xianglin L.
    Wang, Fan
    Zhang, Jing
    Cui, Xiaohai
    Li, Enxiao
    Yang, Jin
    Yi, Min
    Zhang, Yunfeng
    ONCOTARGET, 2017, 8 (63) : 106913 - 106925
  • [9] The impact of early adjuvant chemotherapy in rectal cancer
    Noh, Gyoung Tae
    Han, Jeonghee
    Cho, Min Soo
    Hur, Hyuk
    Lee, Kang Young
    Kim, Nam Kyu
    Min, Byung Soh
    PLOS ONE, 2020, 15 (01):
  • [10] Postoperative adjuvant and salvage radiotherapy for prostate cancer: Impact on freedom from biochemical relapse and survival
    Pacholke, HD
    Wajsman, Z
    Algood, CB
    Morris, CG
    Zlotecki, RA
    UROLOGY, 2004, 64 (05) : 982 - 986