Sustainable Clinical Development of Adjuvant Chemotherapy for Colon Cancer.
Sustainable Clinical Development of Adjuvant Chemotherapy for Colon Cancer.
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DOI:
10.1002/ags3.12503
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发表时间:
2022-01
影响因子:
2.7
通讯作者:
Mori M
中科院分区:
文献类型:
--
作者:
Oki E;Ando K;Taniguchi H;Yoshino T;Mori M
Numerous clinical studies in an adjuvant setting have been conducted and the combination therapy of 5‐fluorouracil and oxaliplatin has been established as the standard treatment for Stage III and as an option for high‐risk Stage II patients. Biologics such as bevacizumab and antiepidermal growth factor receptor antibodies have failed to show additional survival benefits. The indication of adjuvant chemotherapy has been determined according to the pathological stage. Nevertheless, a pathological diagnosis does not necessarily result in selection of the optimal treatment. To improve treatment decisions, many trials have aimed to stratify patients into treatment groups using genomic testing. Recently, gene signature, Immunoscore, and circulating tumor DNA (ctDNA) assays have been reported and among them, ctDNA was shown to be a promising accurate predictive marker for recurrence. Treatment of ctDNA‐positive patients with aggressive chemotherapy may reduce recurrence rates. The ultimate goal is to accurately predict the risk of recurrence and to prevent recurrence in colon cancer patients. In this review we focus on the clinical development of adjuvant chemotherapy and stratification of patients according to risk of recurrence and the future direction of adjuvant chemotherapy. While adjuvant chemotherapy has been shown to reduce the recurrence risk in Stage II and III colon cancer (CC), better prognostic and predictive biomarkers are needed to stratify patients for treatment. In this review we focus on the development of adjuvant chemotherapy and stratification of patients according to risk of recurrence and the future direction of adjuvant chemotherapy.
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影响因子:
5.2
作者:
Chakrabarti S;Xie H;Urrutia R;Mahipal A
通讯作者:
Mahipal A
影响因子:
3.8
作者:
Clark-Langone KM;Sangli C;Krishnakumar J;Watson D
通讯作者:
Watson D
影响因子:
45.3
作者:
Cohen, Romain;Taieb, Julien;Shi, Qian
通讯作者:
Shi, Qian
DOI:
10.1056/nejmoa1713709
发表时间:
2018-03-29
期刊:
The New England journal of medicine
影响因子:
--
作者:
Grothey A;Sobrero AF;Shields AF;Yoshino T;Paul J;Taieb J;Souglakos J;Shi Q;Kerr R;Labianca R;Meyerhardt JA;Vernerey D;Yamanaka T;Boukovinas I;Meyers JP;Renfro LA;Niedzwiecki D;Watanabe T;Torri V;Saunders M;Sargent DJ;Andre T;Iveson T
通讯作者:
Iveson T
影响因子:
3.4
作者:
Huang J;Nair SG;Mahoney MR;Nelson GD;Shields AF;Chan E;Goldberg RM;Gill S;Kahlenberg MS;Quesenberry JT;Thibodeau SN;Smyrk TC;Grothey A;Sinicrope FA;Webb TA;Farr GH Jr;Pockaj BA;Berenberg JL;Mooney M;Sargent DJ;Alberts SR;Alliance for Clinical Trials in Oncology
通讯作者:
Alliance for Clinical Trials in Oncology