Current issues in adjuvant treatment of stage II colon cancer

被引:81
作者
Andre, Thierry
Sargent, Daniel
Tabernero, Josep
O'Connell, Michael
Buyse, Marc
Sobrero, Alberto
Misset, Jean-Louis
Boni, Corrado
de Gramont, Aimery
机构
[1] Hop Tenon, Med Oncol Serv, F-75970 Paris 20, France
[2] Hop St Antoine, CancerEst, F-75571 Paris 12, France
[3] GERCOR, F-75004 Paris, France
[4] Mayo Clin, Rochester, MN 55905 USA
[5] Vall Hebron Univ Hosp, Barcelona 08035, Spain
[6] NSABP Fdn Res Program, Pittsburgh, PA 15212 USA
[7] IDDI, B-1050 Brussels, Belgium
[8] Osped San Martino Genova, I-16132 Genoa, Italy
[9] Hop St Louis, F-75010 Paris, France
[10] Arcispedale S Maria Buova, I-42100 Reggio Emilia, Italy
关键词
colon cancer; stage II; adjuvant chemotherapy; 5-fluorouracil; leucovorin; oxaliplatin;
D O I
10.1245/ASO.2006.07.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Adjuvant chemotherapy with 5-fluorouracil modulated by folinic acid, combined with oxaliplatin, has now become an accepted standard of care for patients with stage III colon cancer. In contrast, the use of adjuvant therapy for stage II patients remains controversial, and the identification of reliable prognostic factors to aid therapeutic decision making is crucial. Methods: The authors critically review the results of clinical trials and meta-analyses investigating the value of adjuvant chemotherapy for stage II patients, emphasizing the heterogeneous nature of this population and the difficulty of performing clinical trials with sufficient power to reliably assess treatment efficacy. They also discuss the evidence concerning potential prognostic factors, particularly molecular markers. Results: Available clinical trial data do not support the routine use of adjuvant chemotherapy for all stage II patients but suggest that it should be considered, particularly for certain high-risk patients. Recent guidelines advocate considering factors such as tumor differentiation, tumor perforation, number of lymph nodes examined, and T stage when assessing the likely benefit:risk ratio. Microsatellite instability and allelic imbalance seem to be strong predictors of good and poor prognosis, respectively, and in the near future, therapeutic decision-making models are likely to be further refined by the inclusion of such molecular markers. Conclusions: There is growing evidence that the prognosis of certain stage II patients with unfavorable prognostic factors can be improved by adjuvant chemotherapy, and increasingly refined tools are now available to define those most likely to benefit. Referral of stage II patients for individual assessment is strongly recommended.
引用
收藏
页码:887 / 898
页数:12
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