Pathological response following long-course neoadjuvant chemoradiotherapy for locally advanced rectal cancer

被引:564
|
作者
Ryan, R [1 ]
Gibbons, D [1 ]
Hyland, JMP [1 ]
Treanor, D [1 ]
White, A [1 ]
Mulcahy, HE [1 ]
O'Donoghue, DP [1 ]
Moriarty, M [1 ]
Fennelly, D [1 ]
Sheahan, K [1 ]
机构
[1] St Vincents Univ Hosp, Ctr Colorectal Dis, Dublin 4, Ireland
关键词
chemoradiotherapy; pathological response; rectal cancer; tumour regression grade;
D O I
10.1111/j.1365-2559.2005.02176.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: To standardize the pathological analysis of total mesorectal excision specimens of rectal cancer following neoadjuvant chemoradiotherapy for locally advanced disease (T3/T4), including tumour regression. Methods and results: Standardized dissection and reporting was used for 60 patients who underwent total mesorectal excision following long-course chemoradiotherapy. Tumour regression was scored by two pathologists (K.S., D.G.) using both an established 5-point tumour regression grade (TRG), and a novel 3-point grade. Both scores were evaluated for interobserver variability. A complete or near-complete pathological response (3-point TRG 1) was found in 10 patients (17%). Using the 5-point TRG, there was good agreement between both pathologists (kappa = 0.64). Using the 3-point grade, agreement was excellent (kappa = 0.84). No disease recurrence has been reported in patients with a complete, or near complete pathological response (3-point TRG 1), after a mean follow-up of 22 months. Conclusion: Tumour regression grade is a useful method of scoring tumour response to chemoradiotherapy in rectal cancer. TRG 1 and 2 can be regarded as a complete pathological response (ypT0). A modified 3-point grade has the advantage of better reproducibility, with similar prognostic significance.
引用
收藏
页码:141 / 146
页数:6
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